Publication catalog

Biomedical publications with connected research

Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.

Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.

Publications

Page 1108 of 10600

Thrombopoietin-induced conformational change in p53 lies downstream of the p44/p42 mitogen activated protein kinase cascade in the human growth factor-dependent cell line M07e.
Oncogene | 1999-02-18 | PMID 10050883
Ritchie A, Braun S E, He J and 1 more
DYT1 mutation in French families with idiopathic torsion dystonia.
Brain : a journal of neurology | 1999-01-01 | PMID 10050893
Lebre A S, Durr A, Jedynak P and 4 more
No association between the intronic presenilin 1 polymorphism and Alzheimer's disease in the Chinese population.
American journal of medical genetics | 1999-02-05 | PMID 10050959
Wu X, Jiang S, Lin S and 6 more
Genes: APOE
Complex segregation analysis for obsessive compulsive disorder and related disorders.
American journal of medical genetics | 1999-02-05 | PMID 10050965
Cavallini M C, Pasquale L, Bellodi L and 1 more
Anticipation is not associated with CAG repeat expansion in parent-offspring pairs of patients affected with schizophrenia.
American journal of medical genetics | 1999-02-05 | PMID 10050967
Martorell L, Pujana M A, Valero J and 5 more
No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder.
American journal of medical genetics | 1999-02-05 | PMID 10050968
Guy C A, Bowen T, Williams N and 6 more
Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder.
American journal of medical genetics | 1999-02-05 | PMID 10050970
Franks E, Guy C, Jacobsen N and 4 more
Intergenerational CAG repeat expansion at ERDA1 in a family with childhood-onset depression, schizoaffective disorder, and recurrent major depression.
American journal of medical genetics | 1999-02-05 | PMID 10050972
Vincent J B, Kovacs M, Krol R and 2 more
Genetic variation in the serotonin transporter promoter region affects serotonin uptake in human blood platelets.
American journal of medical genetics | 1999-02-05 | PMID 10050973
Greenberg B D, Tolliver T J, Huang S J and 3 more
Genes: HTT
102T/C polymorphism of serotonin receptor type 2A gene is not associated with schizophrenia in either Chinese or British populations.
American journal of medical genetics | 1999-02-05 | PMID 10050975
He L, Li T, Melville C and 11 more
Townes-Brocks syndrome.
Journal of medical genetics | 1999-02-01 | PMID 10051003
Powell C M, Michaelis R C
Polymorphisms in PTEN in breast cancer families.
Journal of medical genetics | 1999-02-01 | PMID 10051004
Carroll B T, Couch F J, Rebbeck T R and 1 more
Genes: PTEN
A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.
Journal of medical genetics | 1999-02-01 | PMID 10051005
Froggatt N J, Green J, Brassett C and 4 more
Genes: MSH2, MLH1
Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length.
Journal of medical genetics | 1999-02-01 | PMID 10051007
Kehoe P, Krawczak M, Harper P S and 2 more
Genes: APOE
Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.
Journal of medical genetics | 1999-02-01 | PMID 10051008
Mizushima K, Watanabe M, Kondo I and 5 more
Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis.
Journal of medical genetics | 1999-02-01 | PMID 10051010
Lako M, Ramsden S, Campbell R D and 1 more
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndrome.
Journal of medical genetics | 1999-02-01 | PMID 10051019
Di Rocco M, Arslanian A, Romanengo M and 2 more
Interindividual variation of plasma haloperidol concentrations and the impact of concomitant medications: the analysis of therapeutic drug monitoring data.
Therapeutic drug monitoring | 1999-02-01 | PMID 10051058
Hirokane G, Someya T, Takahashi S and 2 more
Genes: HAL
Biologic variation of serum and salivary lithium.
Therapeutic drug monitoring | 1999-02-01 | PMID 10051061
Moody J P
Therapeutic drug monitoring of risperidone using a new, rapid HPLC method: reappraisal of interindividual variability factors.
Therapeutic drug monitoring | 1999-02-01 | PMID 10051063
Balant-Gorgia A E, Gex-Fabry M, Genet C and 1 more
Transcriptional down-regulation of the rabbit pulmonary artery endothelin B receptor during phenotypic modulation.
British journal of pharmacology | 1999-01-01 | PMID 10051126
Owe-Young R, Schyvens C G, Qasabian R A and 3 more
Acetylcholine-induced relaxation in blood vessels from endothelial nitric oxide synthase knockout mice.
British journal of pharmacology | 1999-01-01 | PMID 10051139
Chataigneau T, Félétou M, Huang P L and 3 more
Selective effects of a 4-oxystilbene derivative on wild and mutant neuronal chick alpha7 nicotinic receptor.
British journal of pharmacology | 1999-01-01 | PMID 10051147
Maggi L, Palma E, Eusebi F and 4 more
Identification of a region of the C-terminal domain involved in short-term desensitization of the prostaglandin EP4 receptor.
British journal of pharmacology | 1999-01-01 | PMID 10051157
Bastepe M, Ashby B
Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.
American journal of medical genetics | 1999-02-12 | PMID 10051161
Mohandas T K, Park J P, Spellman R A and 6 more
Genes: GABRB3, SNRPN
Large kindred with Ehlers-Danlos syndrome type IV due to a point mutation (G571S) in the COL3A1 gene of type III procollagen: low risk of pregnancy complications and unexpected longevity in some affected relatives.
American journal of medical genetics | 1999-02-12 | PMID 10051163
Gilchrist D, Schwarze U, Shields K and 3 more
De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes.
American journal of medical genetics | 1999-02-12 | PMID 10051165
Reddy K S, Sulcova V, Young H and 2 more
Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the Pendred gene.
American journal of medical genetics | 1999-02-12 | PMID 10051166
Abe S, Usami S, Hoover D M and 3 more
Calculating posterior cystic fibrosis risk with echogenic bowel and one characterized cystic fibrosis mutation: avoiding pitfalls in the risk calculations.
American journal of medical genetics | 1999-02-12 | PMID 10051167
Hodge S E, Lebo R V, Yesley A R and 3 more
Genes: CFTR
Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.
American journal of medical genetics | 1999-02-12 | PMID 10051168
Tsai C H, Van Dyke D L, Feldman G L
Plasma platelet-activating factor acetylhydrolase deficiency in Japanese patients with asthma.
American journal of respiratory and critical care medicine | 1999-03-01 | PMID 10051281
Satoh N, Asano K, Naoki K and 4 more
G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men.
Circulation | 1999-03-02 | PMID 10051291
Ridker P M, Hennekens C H, Miletich J P
PlA polymorphism of platelet glycoprotein IIIa and risk of restenosis after coronary stent placement.
Circulation | 1999-03-02 | PMID 10051292
Kastrati A, Schömig A, Seyfarth M and 6 more
Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.
Circulation | 1999-03-02 | PMID 10051298
Lazarus A, Varin J, Ounnoughene Z and 8 more
The mouse mutation Pdn (Polydactyly Nagoya) is caused by the integration of a retrotransposon into the Gli3 gene.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051311
Thien H, Rüther U
Jumbled spine and ribs (Jsr): a new mutation on mouse chromosome 5.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051313
Miyoshi H, Kon Y, Seo K W and 3 more
Genes: MOG
Cloning of the mouse organic cation transporter 2 gene, Slc22a2, from an enhancer-trap transgene integration locus.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051314
Mooslehner K A, Allen N D
Quantitative trait loci for growth traits in C57BL/6J x DBA/2J mice.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051315
Morris K H, Ishikawa A, Keightley P D
Genetic typing of the senescence-accelerated mouse (SAM) strains with microsatellite markers.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051317
Xia C, Higuchi K, Shimizu M and 6 more
Genetic localization and transmission of the mouse osteopetrotic grey-lethal mutation.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051318
Vacher J, Bernard H
Mapping and characterization of quantitative trait loci for non-insulin-dependent diabetes mellitus with an improved genetic map in the Otsuka Long-Evans Tokushima fatty rat.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051320
Wei S, Wei K, Moralejo D H and 7 more
Complete genome searches for quantitative trait loci controlling blood pressure and related traits in four segregating populations derived from Dahl hypertensive rats.
Mammalian genome : official journal of the International Mammalian Genome Society | 1999-03-01 | PMID 10051321
Kato N, Hyne G, Bihoreau M T and 3 more
Phylogenetic relations among percid fishes as inferred from mitochondrial cytochrome b DNA sequence data.
Molecular phylogenetics and evolution | 1998-12-01 | PMID 10051387
Song C B, Near T J, Page L M
Molecular phylogenetics of finches and sparrows: consequences of character state removal in cytochrome b sequences.
Molecular phylogenetics and evolution | 1998-12-01 | PMID 10051390
Groth J G
Molecular phylogeny and biogeography of the marine shrimp Penaeus.
Molecular phylogenetics and evolution | 1998-12-01 | PMID 10051392
Baldwin J D, Bass A L, Bowen B W and 1 more
Phylogenetic analysis of southern hemisphere flat oysters based on partial mitochondrial 16S rDNA gene sequences.
Molecular phylogenetics and evolution | 1998-12-01 | PMID 10051395
Jozefowicz C J, Foighil D O
Phylogenetic utility of the external transcribed spacer (ETS) of 18S-26S rDNA: congruence of ETS and ITS trees of Calycadenia (Compositae).
Molecular phylogenetics and evolution | 1998-12-01 | PMID 10051397
Baldwin B G, Markos S
Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family.
Genomics | 1999-03-01 | PMID 10051399
Ahmad W, Zlotogorski A, Panteleyev A A and 6 more
Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp).
Genomics | 1999-03-01 | PMID 10051400
Eddleston J, Murdoch J N, Copp A J and 1 more
Structure of the human palmitoyl-protein thioesterase-2 gene (PPT2) in the major histocompatibility complex on chromosome 6p21.3.
Genomics | 1999-03-01 | PMID 10051407
Soyombo A A, Yi W, Hofmann S L
Genes: PPT2, NCL, PPT1
Plasmalogens as endogenous antioxidants: somatic cell mutants reveal the importance of the vinyl ether.
The Biochemical journal | 1999-03-15 | PMID 10051451
Zoeller R A, Lake A C, Nagan N and 3 more
A p53 genetic polymorphism as a modulator of hepatocellular carcinoma risk in relation to chronic liver disease, familial tendency, and cigarette smoking in hepatitis B carriers.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051470
Yu M W, Yang S Y, Chiu Y H and 3 more
The human p53 gene mutated at position 249 per se is not sufficient to immortalize human liver cells.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051487
Schleger C, Becker R, Oesch F and 1 more
Control of the tissue inhibitor of metalloproteinases-1 promoter in culture-activated rat hepatic stellate cells: regulation by activator protein-1 DNA binding proteins.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051488
Bahr M J, Vincent K J, Arthur M J and 7 more
Efficacy of lamivudine in patients with hepatitis B e antigen-negative/hepatitis B virus DNA-positive (precore mutant) chronic hepatitis B. Lamivudine Precore Mutant Study Group.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051494
Tassopoulos N C, Volpes R, Pastore G and 7 more
Hepatitis B virus X protein transactivates the inducible nitric oxide synthase promoter.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051498
Amaro M J, Bartolomé J, Carreño V
Genes: CAT
YMDD motif in hepatitis B virus DNA polymerase influences on replication and lamivudine resistance: A study by in vitro full-length viral DNA transfection.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051501
Ono-Nita S K, Kato N, Shiratori Y and 4 more
High prevalence of 1762(T) 1764(A) mutations in the basic core promoter of hepatitis B virus isolated from black Africans with hepatocellular carcinoma compared with asymptomatic carriers.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051502
Baptista M, Kramvis A, Kew M C
Different hepatitis B virus genotypes are associated with different mutations in the core promoter and precore regions during hepatitis B e antigen seroconversion.
Hepatology (Baltimore, Md.) | 1999-03-01 | PMID 10051506
Chan H L, Hussain M, Lok A S
Mutations in the S4 region isolate the final voltage-dependent cooperative step in potassium channel activation.
The Journal of general physiology | 1999-03-01 | PMID 10051516
Ledwell J L, Aldrich R W
Suppression of replication of multidrug-resistant HIV type 1 variants by combinations of thymidylate synthase inhibitors with zidovudine or stavudine.
Molecular pharmacology | 1999-03-01 | PMID 10051538
Gao W Y, Johns D G, Tanaka M and 1 more
Role of a conserved lysine residue in the peripheral cannabinoid receptor (CB2): evidence for subtype specificity.
Molecular pharmacology | 1999-03-01 | PMID 10051546
Tao Q, McAllister S D, Andreassi J and 7 more
Angiopoietins 3 and 4: diverging gene counterparts in mice and humans.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051567
Valenzuela D M, Griffiths J A, Rojas J and 12 more
Cytochrome P450 CYP1B1 determines susceptibility to 7, 12-dimethylbenz[a]anthracene-induced lymphomas.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051580
Buters J T, Sakai S, Richter T and 7 more
Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051618
Ghosh S, Watanabe R M, Hauser E R and 37 more
Localization of non-Mhc collagen-induced arthritis susceptibility loci in DBA/1j mice.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051620
McIndoe R A, Bohlman B, Chi E and 3 more
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051637
Pelin K, Hilpelä P, Donner K and 17 more
Genes: TPM3
Mutated epithelial cadherin is associated with increased tumorigenicity and loss of adhesion and of responsiveness to the motogenic trefoil factor 2 in colon carcinoma cells.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051639
Efstathiou J A, Liu D, Wheeler J M and 9 more
Genes: CDH1
Analysis of masked mutations in familial adenomatous polyposis.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051640
Laken S J, Papadopoulos N, Petersen G M and 6 more
Genes: APC, FAP
Overexpression of a Shaker-type potassium channel in mammalian central nervous system dysregulates native potassium channel gene expression.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051663
Sutherland M L, Williams S H, Abedi R and 3 more
A neomorphic syntaxin mutation blocks volatile-anesthetic action in Caenorhabditis elegans.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051668
van Swinderen B, Saifee O, Shebester L and 3 more
Reverse genetic analysis of Caenorhabditis elegans presenilins reveals redundant but unequal roles for sel-12 and hop-1 in Notch-pathway signaling.
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051671
Westlund B, Parry D, Clover R and 2 more
Two gonadotropin-releasing hormone receptor subtypes with distinct ligand selectivity and differential distribution in brain and pituitary in the goldfish (Carassius auratus).
Proceedings of the National Academy of Sciences of the United States of America | 1999-03-02 | PMID 10051676
Illing N, Troskie B E, Nahorniak C S and 3 more
Immunogenetics of atopic asthma: association of DRB1*1101 DQA1*0501 DQB1*0301 haplotype with Dermatophagoides spp.-sensitive asthma in a sample of the Venezuelan population.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology | 1999-01-01 | PMID 10051703
Lara-Marquez M L, Yunis J J, Layrisse Z and 7 more
Lack of association of atopy/asthma and the interleukin-4 receptor alpha gene in Japanese.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology | 1999-02-01 | PMID 10051727
Noguchi E, Shibasaki M, Arinami T and 7 more
Excitatory synaptic transmission and its modulation by PKC is unchanged in the hippocampus of GAP-43-deficient mice.
The European journal of neuroscience | 1999-02-01 | PMID 10051744
Capogna M, Fankhauser C, Gagliardini V and 2 more
Chronic morphine exposure and spontaneous withdrawal are associated with modifications of dopamine receptor and neuropeptide gene expression in the rat striatum.
The European journal of neuroscience | 1999-02-01 | PMID 10051749
Georges F, Stinus L, Bloch B and 1 more
[Markers for risk of IDDM in children of Danish patients with IDDM. A population-based, historical prospective study].
Ugeskrift for laeger | 1999-02-15 | PMID 10051805
Lorenzen T, Pociot F, Stilgren L S and 9 more
Protein carbonyl accumulation in aging dauer formation-defective (daf) mutants of Caenorhabditis elegans.
The journals of gerontology. Series A, Biological sciences and medical sciences | 1999-02-01 | PMID 10051850
Yasuda K, Adachi H, Fujiwara Y and 1 more
Age-related phenotypic alterations in populations of purified human bone precursor cells.
The journals of gerontology. Series A, Biological sciences and medical sciences | 1999-02-01 | PMID 10051851
Long M W, Ashcraft E K, Normalle D and 1 more
Thermostability reinforcement through a combination of thermostability-related mutations of N-carbamyl-D-amino acid amidohydrolase.
Bioscience, biotechnology, and biochemistry | 1999-01-01 | PMID 10052127
Ikenaka Y, Nanba H, Yajima K and 3 more
Cloning and characterization of chemotaxis genes in Pseudomonas aeruginosa.
Bioscience, biotechnology, and biochemistry | 1999-01-01 | PMID 10052136
Kato J, Nakamura T, Kuroda A and 1 more
gigas, a Drosophila homolog of tuberous sclerosis gene product-2, regulates the cell cycle.
Cell | 1999-02-19 | PMID 10052455
Ito N, Rubin G M
Genes: TSC1, TSC2
Transducing the Dpp morphogen gradient in the wing of Drosophila: regulation of Dpp targets by brinker.
Cell | 1999-02-19 | PMID 10052457
Campbell G, Tomlinson A
The Drosophila gene brinker reveals a novel mechanism of Dpp target gene regulation.
Cell | 1999-02-19 | PMID 10052458
Jaźwińska A, Kirov N, Wieschaus E and 2 more
Genetic heterogeneity of Escherichia coli O157:H7 in Scotland and its utility in strain subtyping.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 1998-12-01 | PMID 10052547
Allison L, Stirrat A, Thomson-Carter F M
Common fragile site expression and genetic predisposition to breast cancer.
Teratogenesis, carcinogenesis, and mutagenesis | 1998-01-01 | PMID 10052563
Ceçener G, Egeli U, Taşdelen I and 3 more
Associations between amino acids in the evolution of HIV type 1 protease sequences under indinavir therapy.
AIDS research and human retroviruses | 1999-02-10 | PMID 10052755
Brown A J, Korber B T, Condra J H
Prognosis versus actual outcome. IV. The effectiveness of clinical parameters and IL-1 genotype in accurately predicting prognoses and tooth survival.
Journal of periodontology | 1999-01-01 | PMID 10052770
McGuire M K, Nunn M E
The effect of reserpine, an inhibitor of multidrug efflux pumps, on the in-vitro activities of ciprofloxacin, sparfloxacin and moxifloxacin against clinical isolates of Staphylococcus aureus.
The Journal of antimicrobial chemotherapy | 1998-12-01 | PMID 10052906
Schmitz F J, Fluit A C, Lückefahr M and 6 more
In-vitro selection of porin-deficient mutants of two strains of Klebsiella pneumoniae with reduced susceptibilities to meropenem, but not to imipenem.
The Journal of antimicrobial chemotherapy | 1998-12-01 | PMID 10052909
Pragai Z, Nagy E
Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B.
American journal of human genetics | 1999-03-01 | PMID 10053004
Reiss J, Dorche C, Stallmeyer B and 3 more
Genes: MOCS2, MOCS1
Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development.
American journal of human genetics | 1999-03-01 | PMID 10053005
Kosaki K, Bassi M T, Kosaki R and 4 more
A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.
American journal of human genetics | 1999-03-01 | PMID 10053006
Tavormina P L, Bellus G A, Webster M K and 11 more
Genes: FGFR3
Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
American journal of human genetics | 1999-03-01 | PMID 10053007
Sybert V P, Francis J S, Corden L D and 4 more
Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome.
American journal of human genetics | 1999-03-01 | PMID 10053008
Toh S, Wada M, Uchiumi T and 6 more
Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.
American journal of human genetics | 1999-03-01 | PMID 10053009
Funke B, Edelmann L, McCain N and 7 more
Genes: RANBP1, ZNF74
Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.
American journal of human genetics | 1999-03-01 | PMID 10053010
Plenge R M, Tranebjaerg L, Jensen P K and 2 more
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.
American journal of human genetics | 1999-03-01 | PMID 10053011
Richter A, Rioux J D, Bouchard J P and 10 more
Genes: SGCG
Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36.
American journal of human genetics | 1999-03-01 | PMID 10053012
Gibbs M, Stanford J L, McIndoe R A and 11 more