Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis.
The Journal of investigative dermatology | 1997-10-01 | PMID 9326398
Korge B P, Ishida-Yamamoto A, Pünter C and 5 more
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.
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Publications
Page 901 of 10600
Strategies for determining HLA compatibility in related donor bone marrow transplantation.
Transplantation | 1997-09-27 | PMID 9326406
Zachary A A, Vogelsang G B, Steinberg A G and 1 more
Segregation analysis of prostate cancer in Sweden: support for dominant inheritance.
American journal of epidemiology | 1997-10-01 | PMID 9326432
Grönberg H, Damber L, Damber J E and 1 more
Power and sample size calculations for case-control studies of gene-environment interactions with a polytomous exposure variable.
American journal of epidemiology | 1997-10-01 | PMID 9326439
Foppa I, Spiegelman D
Effect of strain on human keratinocytes in vitro.
Journal of cellular physiology | 1997-10-01 | PMID 9326450
Takei T, Rivas-Gotz C, Delling C A and 5 more
Interleukin-1 induces major phenotypic changes in human skin microvascular endothelial cells.
Journal of cellular physiology | 1997-10-01 | PMID 9326452
Romero L I, Zhang D N, Herron G S and 1 more
Dependence of mesenchymal cell responses on duration of exposure to bone morphogenetic protein-2 in vitro.
Journal of cellular physiology | 1997-10-01 | PMID 9326453
Puleo D A
The yeast Prp3 protein is a U4/U6 snRNP protein necessary for integrity of the U4/U6 snRNP and the U4/U6.U5 tri-snRNP.
RNA (New York, N.Y.) | 1997-10-01 | PMID 9326489
Anthony J G, Weidenhammer E M, Woolford J L
Probing the structure of the regulatory region of human transferrin receptor messenger RNA and its interaction with iron regulatory protein-1.
RNA (New York, N.Y.) | 1997-10-01 | PMID 9326491
Schlegl J, Gegout V, Schläger B and 5 more
A yeast sterol auxotroph (erg25) is rescued by addition of azole antifungals and reduced levels of heme.
Proceedings of the National Academy of Sciences of the United States of America | 1997-10-14 | PMID 9326581
Gachotte D, Pierson C A, Lees N D and 3 more
A phylogenetic perspective on P transposable element evolution in Drosophila.
Proceedings of the National Academy of Sciences of the United States of America | 1997-10-14 | PMID 9326626
Clark J B, Kidwell M G
The atypical codon usage of the plant psbA gene may be the remnant of an ancestral bias.
Proceedings of the National Academy of Sciences of the United States of America | 1997-10-14 | PMID 9326627
Morton B R, Levin J A
Cleft palate in mice with a targeted mutation in the gamma-aminobutyric acid-producing enzyme glutamic acid decarboxylase 67.
Proceedings of the National Academy of Sciences of the United States of America | 1997-10-14 | PMID 9326630
Condie B G, Bain G, Gottlieb D I and 1 more
A dominant form of inherited retinal degeneration caused by a non-photoreceptor cell-specific mutation.
Proceedings of the National Academy of Sciences of the United States of America | 1997-10-14 | PMID 9326664
Li L, Dowling J E
Genes: ERG
Arabidopsis thaliana mutants altered in homologous recombination.
Proceedings of the National Academy of Sciences of the United States of America | 1997-10-14 | PMID 9326679
Masson J E, Paszkowski J
Three CAG trinucleotide repeats on chromosome 6 (D6S1014, D6S1015, and D6S1058) are not expanded in 30 families with schizophrenia.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology | 1997-10-01 | PMID 9326753
Ohara K, Tani K, Tsukamoto T and 7 more
Possible association of a polymorphism of the tryptophan hydroxylase gene with suicidal behavior in depressed patients.
The American journal of psychiatry | 1997-10-01 | PMID 9326831
Mann J J, Malone K M, Nielsen D A and 3 more
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.
Nature genetics | 1997-10-01 | PMID 9326933
Hildebrandt F, Otto E, Rensing C and 5 more
Genes: NPHP1, MALL
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.
Nature genetics | 1997-10-01 | PMID 9326936
Simon D B, Bindra R S, Mansfield T A and 18 more
Genes: CLCNKB, CLCNKA
Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation.
Nature genetics | 1997-10-01 | PMID 9326937
Lu W, Peissel B, Babakhanlou H and 6 more
Genes: PKD1
Male-driven evolution of DNA sequences in birds.
Nature genetics | 1997-10-01 | PMID 9326938
Ellegren H, Fridolfsson A K
Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene.
Nature genetics | 1997-10-01 | PMID 9326940
Jansen G A, Ofman R, Ferdinandusse S and 8 more
Genes: PHYH
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
Nature genetics | 1997-10-01 | PMID 9326941
Gu S M, Thompson D A, Srikumari C R and 8 more
Genes: RPE, RPE65
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa.
Nature genetics | 1997-10-01 | PMID 9326942
Maw M A, Kennedy B, Knight A and 7 more
Genes: RLBP1, RPE
The genetic and functional basis of isolated 17,20-lyase deficiency.
Nature genetics | 1997-10-01 | PMID 9326943
Geller D H, Auchus R J, Mendonça B B and 1 more
Drosophila CBP is required for dorsal-dependent twist gene expression.
Nature genetics | 1997-10-01 | PMID 9326945
Akimaru H, Hou D X, Ishii S
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
Nature genetics | 1997-10-01 | PMID 9326946
Rötig A, de Lonlay P, Chretien D and 5 more
Genes: GAA
Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.
Nature genetics | 1997-10-01 | PMID 9326947
Pereira L, Andrikopoulos K, Tian J and 9 more
Genes: FBN1
Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome.
Nature genetics | 1997-10-01 | PMID 9326952
McGrath J A, McMillan J R, Shemanko C S and 5 more
Genes: PKP1
Abnormal skeletal muscle bioenergetics in familial hypertrophic cardiomyopathy.
Heart (British Cardiac Society) | 1997-08-01 | PMID 9326994
Thompson C H, Kemp G J, Taylor D J and 6 more
Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease.
QJM : monthly journal of the Association of Physicians | 1997-08-01 | PMID 9327029
van der Put N M, van der Molen E F, Kluijtmans L A and 6 more
No evidence for the influence of HLA class II in alleles in isocyanate-induced asthma.
American journal of industrial medicine | 1997-11-01 | PMID 9327077
Rihs H P, Barbalho-Krölls T, Huber H and 1 more
ApoE genotype and Alzheimer's disease in adults with Down syndrome: meta-analysis.
American journal of mental retardation : AJMR | 1997-09-01 | PMID 9327086
Prasher V P, Chowdhury T A, Rowe B R and 1 more
Genetic construction and characterization of an anti-monkey CD3 single-chain immunotoxin with a truncated diphtheria toxin.
Bioconjugate chemistry | 2000-01-01 | PMID 9327133
Ma S, Hu H, Thompson J and 3 more
Prognostic implications of c-Ki-ras2 mutations in patients with advanced colorectal cancer treated with 5-fluorouracil and interferon: a study of the eastern cooperative oncology group (EST 2292)
The cancer journal from Scientific American | 2000-01-01 | PMID 9327152
Wadler S, Bajaj R, Neuberg D and 3 more
Recent advances in lymphoma biology.
Current opinion in oncology | 1997-09-01 | PMID 9327217
Ghia P, Nadler L M
Human omental microvascular endothelial and mesothelial cells: characterization of two distinct mesodermally derived epithelial cells.
Microvascular research | 1997-09-01 | PMID 9327382
Chung-Welch N, Patton W F, Shepro D and 1 more
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'.
Neuromuscular disorders : NMD | 1997-09-01 | PMID 9327403
Rubio J C, Martín M A, Bautista J and 3 more
Increased species diversity and extended habitat range of sulfur-oxidizing Thiomicrospira spp.
Applied and environmental microbiology | 1997-10-01 | PMID 9327542
Brinkhoff T, Muyzer G
The freeze-thaw stress response of the yeast Saccharomyces cerevisiae is growth phase specific and is controlled by nutritional state via the RAS-cyclic AMP signal transduction pathway.
Applied and environmental microbiology | 1997-10-01 | PMID 9327544
Park J I, Grant C M, Attfield P V and 1 more
Critical role of anteiso-C15:0 fatty acid in the growth of Listeria monocytogenes at low temperatures.
Applied and environmental microbiology | 1997-10-01 | PMID 9327552
Annous B A, Becker L A, Bayles D O and 2 more
Phenotypic and genotypic biotyping of environmental strains of Vibrio cholerae non-O1 isolated in Italy.
Applied and environmental microbiology | 1997-10-01 | PMID 9327577
Filetici E, Bonadonna L, Ciccozzi M and 3 more
The gene encoding flavanone 3-hydroxylase is expressed normally in the pale yellow flowers of the Japanese morning glory carrying the speckled mutation which produce neither flavonol nor anthocyanin but accumulate chalcone, aurone and flavanone.
Plant & cell physiology | 1997-08-01 | PMID 9327594
Hoshino A, Abe Y, Saito N and 2 more
An unusual mitochondrial atp9-rpl16 cotranscript found in the maternal distorted leaf mutant of Arabidopsis thaliana: implication of GUG as an initiation codon in plant mitochondria.
Plant & cell physiology | 1997-08-01 | PMID 9327595
Sakamoto W, Tan S H, Murata M and 1 more
Allelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas.
The American journal of pathology | 1997-10-01 | PMID 9327728
Vortmeyer A O, Lubensky I A, Fogt F and 3 more
Genes: VHL
A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).
Arteriosclerosis, thrombosis, and vascular biology | 1997-09-01 | PMID 9327760
Cattaneo M, Tsai M Y, Bucciarelli P and 4 more
Genes: MTHFR
Alu-repeat polymorphism in the gene coding for tissue-type plasminogen activator (t-PA) and risks of myocardial infarction among middle-aged men.
Arteriosclerosis, thrombosis, and vascular biology | 1997-09-01 | PMID 9327764
Ridker P M, Baker M T, Hennekens C H and 2 more
Genetic variation in factor VII associated with variation in plasma lipoprotein(a) concentration.
Arteriosclerosis, thrombosis, and vascular biology | 1997-09-01 | PMID 9327766
Hegele R A, Breckenridge W C, Brunt J H and 1 more
HDL deficiency in genetically engineered mice requires elevated LDL to accelerate atherogenesis.
Arteriosclerosis, thrombosis, and vascular biology | 1997-09-01 | PMID 9327769
Hughes S D, Verstuyft J, Rubin E M
The II genotype of the angiotensin-converting enzyme gene delays the onset of acute coronary syndromes.
Arteriosclerosis, thrombosis, and vascular biology | 1997-09-01 | PMID 9327770
Iwai N, Tamaki S, Ohmichi N and 1 more
Genes: ACE
Dietary fat clearance in normal subjects is modulated by genetic variation at the apolipoprotein B gene locus.
Arteriosclerosis, thrombosis, and vascular biology | 1997-09-01 | PMID 9327775
Lopez-Miranda J, Ordovas J M, Ostos M A and 7 more
Induction of chromosome-specific aneuploidy and micronuclei in human lymphocytes by metabolites of 1,3-butadiene.
Carcinogenesis | 1997-09-01 | PMID 9328162
Xi L, Zhang L, Wang Y and 1 more
Smad4 (homolog of human DPC4) and Smad2 (homolog of human JV18-1): candidates for murine lung tumor resistance and suppressor genes.
Carcinogenesis | 1997-09-01 | PMID 9328171
Devereux T R, Anna C H, Patel A C and 3 more
Both estradiol and tamoxifen decrease proliferation and invasiveness of cancer cells transfected with a mutated estrogen receptor.
The Journal of steroid biochemistry and molecular biology | 1997-04-01 | PMID 9328205
Garcia M, Derocq D, Platet N and 4 more
Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndrome.
The Journal of steroid biochemistry and molecular biology | 1997-04-01 | PMID 9328206
Bevan C L, Hughes I A, Patterson M N
GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs.
Journal of neurology, neurosurgery, and psychiatry | 1997-09-01 | PMID 9328244
Jarman P R, Bandmann O, Marsden C D and 1 more
Genes: GCH1
Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affected.
Journal of neurology, neurosurgery, and psychiatry | 1997-09-01 | PMID 9328258
Wicklein E M, Orth U, Gal A and 1 more
Aryl hydrocarbon (Ah) nonresponsiveness in estrogen receptor-negative MDA-MB-231 cells is associated with expression of a variant arnt protein.
Archives of biochemistry and biophysics | 1997-10-01 | PMID 9328285
Wilson C L, Thomsen J, Hoivik D J and 4 more
Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families.
Hepatology (Baltimore, Md.) | 1997-10-01 | PMID 9328324
Adams P C, Campion M L, Gandon G and 3 more
Genes: HFE
Prevalence, risk factors, and genotype distribution of hepatitis C virus infection in the general population: a community-based survey in southern Italy.
Hepatology (Baltimore, Md.) | 1997-10-01 | PMID 9328327
Guadagnino V, Stroffolini T, Rapicetta M and 10 more
HLA-C genes and susceptibility to type 1 autoimmune hepatitis.
Hepatology (Baltimore, Md.) | 1997-10-01 | PMID 9328330
Strettell M D, Thomson L J, Donaldson P T and 3 more
Analysis of the role of E2A-encoded proteins in insulin gene transcription.
Molecular endocrinology (Baltimore, Md.) | 1997-10-01 | PMID 9328343
Sharma A, Henderson E, Gamer L and 2 more
Colony-stimulating factor-1 plays a major role in the development of reproductive function in male mice.
Molecular endocrinology (Baltimore, Md.) | 1997-10-01 | PMID 9328346
Cohen P E, Hardy M P, Pollard J W
Stage-specific expression of Dlx-5 during osteoblast differentiation: involvement in regulation of osteocalcin gene expression.
Molecular endocrinology (Baltimore, Md.) | 1997-10-01 | PMID 9328350
Ryoo H M, Hoffmann H M, Beumer T and 6 more
Effect of increasing serum albumin on serum lipoprotein(a) concentration in patients receiving CAPD.
American journal of kidney diseases : the official journal of the National Kidney Foundation | 1997-10-01 | PMID 9328365
Yang W S, Min W K, Park J S and 1 more
Comparison of chemical carcinogen skin tumor induction efficacy in inbred, mutant, and hybrid strains of mice: morphologic variations of induced tumors and absence of a papillomavirus cocarcinogen.
Molecular carcinogenesis | 1997-09-01 | PMID 9328433
Sundberg J P, Sundberg B A, Beamer W G
Decreases in phorbol ester-induced papilloma development in v-Ha-ras transgenic TG.AC mice during reduced gene dosage of bcl-2.
Molecular carcinogenesis | 1997-09-01 | PMID 9328437
Trempus C S, Haseman J K, Tennant R W
Evidence that mirex promotes a unique population of epidermal cells that cannot be distinguished by their mutant Ha-ras genotype.
Molecular carcinogenesis | 1997-09-01 | PMID 9328442
Kim T W, Porter K L, Foley J F and 2 more
Genes: PCNA
New strains of inbred SENCAR mice with increased susceptibility to induction of papillomas and squamous cell carcinomas in skin.
Molecular carcinogenesis | 1997-09-01 | PMID 9328445
Hennings H, Lowry D T, Yuspa S H and 2 more
Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing patterns in different cell types.
Human molecular genetics | 1997-11-01 | PMID 9328464
Kilian A, Bowtell D D, Abud H E and 6 more
The human GARS-AIRS-GART gene encodes two proteins which are differentially expressed during human brain development and temporally overexpressed in cerebellum of individuals with Down syndrome.
Human molecular genetics | 1997-11-01 | PMID 9328467
Brodsky G, Barnes T, Bleskan J and 3 more
Genes: GART
Germline mutations of the CDKN2 gene in UK melanoma families.
Human molecular genetics | 1997-11-01 | PMID 9328469
Harland M, Meloni R, Gruis N and 10 more
Genes: CDK4, CDK6
Higher proportion of intact exon 9 CFTR mRNA in nasal epithelium compared with vas deferens.
Human molecular genetics | 1997-11-01 | PMID 9328474
Mak V, Jarvi K A, Zielenski J and 2 more
Genes: CFTR
Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19.
Human molecular genetics | 1997-11-01 | PMID 9328475
Semina E V, Reiter R S, Murray J C
Distortion of allelic expression of apolipoprotein E in Alzheimer's disease.
Human molecular genetics | 1997-11-01 | PMID 9328480
Lambert J C, Pérez-Tur J, Dupire M J and 6 more
Genes: APOE
Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosis.
Human molecular genetics | 1997-11-01 | PMID 9328481
Jones A C, Daniells C E, Snell R G and 5 more
Genes: TSC1, TSC2, PKD1
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Human molecular genetics | 1997-11-01 | PMID 9328482
Carrasquillo M M, Zlotogora J, Barges S and 1 more
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
Human molecular genetics | 1997-11-01 | PMID 9328483
Tyson J, Tranebjaerg L, Bellman S and 10 more
Detection of colorectal cancer K-ras mutations using a simplified oligonucleotide ligation assay.
Journal of immunological methods | 1997-08-07 | PMID 9328563
Rothschild C B, Brewer C S, Loggie B and 2 more
The appearance of the CD4+CD8+ phenotype on activated T cells: possible role of antigen transfer.
Human immunology | 1997-06-01 | PMID 9328784
Rabinowitz R, Hadar R, Schlesinger M
Peptide recognition by T-cell clones of an HLA-DRB1*1501/*0901 heterozygous donor is promiscuous only between parental alleles.
Human immunology | 1997-06-01 | PMID 9328787
Agrewala J N, Deacock S, Jurcevic S and 1 more
HLA-DQ alleles associate with cutaneous features of onchocerciasis. The Kaduna-London-Manchester Collaboration for Research on Onchocerciasis.
Human immunology | 1997-06-01 | PMID 9328789
Murdoch M E, Payton A, Abiose A and 6 more
HLA class I and class II allele and haplotype distribution in the Venezuelan population.
Human immunology | 1997-06-01 | PMID 9328790
Makhatadze N J, Franco M T, Layrisse Z
HLA-DR and -DQ associations with multiple sclerosis in Turkey.
Human immunology | 1997-06-01 | PMID 9328791
Saruhan-Direskeneli G, Esin S, Baykan-Kurt B and 3 more
Polymorphism at codons 114, 116, 145, and 163 muddle the typing of HLA-B*1304.
Human immunology | 1997-06-01 | PMID 9328792
Ellexson M, Lai-Kwan P, Lau M and 5 more
A comparative study of HLA-DRB typing by transcription-mediated amplification with the hybridization protection assay (TMA/HPA) versus PCR/SSOP.
Human immunology | 1997-06-01 | PMID 9328793
Smith A G, Matsubara K, Mickelson E and 4 more
v-erbA oncogene initiates ultrastructural changes characteristic of early and intermediate events of meiotic maturation in Xenopus oocytes.
Journal of cellular biochemistry | 1997-11-01 | PMID 9328824
Nagl S B, Bunn C F, Allison L A
Reduced utilization of Man5GlcNAc2-P-P-lipid in a Lec9 mutant of Chinese hamster ovary cells: analysis of the steps in oligosaccharide-lipid assembly.
Journal of cellular biochemistry | 1997-11-01 | PMID 9328825
Hall C W, McLachlan K R, Krag S S and 1 more
Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria.
Kidney international | 1997-10-01 | PMID 9328927
Nakazato H, Hattori S, Furuse A and 6 more
Genes: CLCN5
Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
Kidney international | 1997-10-01 | PMID 9328929
Akuta N, Lloyd S E, Igarashi T and 5 more
Genes: CLCN5
Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group.
Headache | 1997-09-01 | PMID 9329229
Ophoff R A, Terwindt G M, Vergouwe M N and 2 more
A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329347
Wada N, Chiba H, Shimizu C and 3 more
Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329356
Jääskeläinen J, Levo A, Voutilainen R and 1 more
Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329371
Hegele R A, Connelly P W, Scherer S W and 4 more
Genes: PON2
A case of metastatic medullary thyroid carcinoma: early identification before surgery of an RET proto-oncogene somatic mutation in fine-needle aspirate specimens.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329372
Russo D, Arturi F, Chiefari E and 4 more
Genes: RET
Molecular scanning of beta-3-adrenergic receptor gene in total congenital lipoatrophic diabetes mellitus.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329375
Silver K, Walston J, Plotnick L and 3 more
Detection of skewed X-inactivation in two female carriers of vasopressin type 2 receptor gene mutation.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329382
Nomura Y, Onigata K, Nagashima T and 4 more
Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329385
Pinto G, Netchine I, Sobrier M L and 3 more
Genes: GHRH, PRL
Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329388
Biebermann H, Schöneberg T, Krude H and 3 more
Genes: TSHR
A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation.
The Journal of clinical endocrinology and metabolism | 1997-10-01 | PMID 9329390
Giraud S, Choplin H, Teh B T and 7 more
Genes: MEN1