Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Polymorphism in and localization of the gene LCP2 (SLP-76) to chromosome 5q33.1-qter.

Genomics - 1 Jul 1996

Sunden S L, Carr L L, Clements J L, Motto D G, Koretzky G A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adaptor Proteins, Signal Transducing
Share to Base Sequence
Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 5

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hematopoietic Stem Cells

Share to Lod Score

Share to Phosphoproteins

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 8661136
DOI: 10.1006/geno.1996.0354

Genes

LCP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polymorphism in and localization of the gene LCP2 (SLP-76) to chromosome 5q33.1-qter.PMID 8661136Read ↗

Physical mapping of distinct 7q22 deletions in uterine leiomyoma and analysis of a recently annotated 7q22 candidate gene.Semantic proximity Read ↗

A novel compound heterozygous variant in the LLS gene is associated with nonsyndromic hypotrichosis.Semantic proximity Read ↗

Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s.Semantic proximity Read ↗

C306A single nucleotide polymorphism in the human CEBPD gene that maps at 8p11.1-p11.2.Semantic proximity Read ↗

Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.Semantic proximity Read ↗

Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.Semantic proximity Read ↗

Two novel polymorphisms (c954T>C and c1038A>G) in exon8 of NPHS2 gene identified in Taiwan Chinese.Semantic proximity Read ↗

LCAT deficiency: molecular and phenotypic characterization of an Italian family.Semantic proximity Read ↗

Identification of a Locus for Progressive Familial Intrahepatic Cholestasis PFIC2on Chromosome 2q24Semantic proximity Read ↗

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneitySemantic proximity Read ↗

Structure and chromosome localization of the human CASP8 geneSemantic proximity Read ↗

Linkage analysis in a large family with primary pulmonary hypertension: genetic heterogeneity and a second primary pulmonary hypertension locus on 2q31-32.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.