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Article

A high frequency polymorphism in the candidate region for tuberous sclerosis 1 (TSC1) at 9q34.

Annals of human genetics - 1 May 1996

Mor O, Duhig T, Fried M

Abstract excerpt

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Topics

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Share to Chromosomes, Human, Pair 9
Share to Electrophoresis, Polyacrylamide Gel
Share to Gene Frequency
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Heterozygote

Share to Homozygote

Share to Polymorphism, Single-Stranded Conformational

Share to Tuberous Sclerosis

Source

Identifiers

PMID: 8800442
DOI: 10.1111/j.1469-1809.1996.tb00429.x

Genes

TSC1

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A high frequency polymorphism in the candidate region for tuberous sclerosis 1 (TSC1) at 9q34.PMID 8800442Read ↗

A high-resolution linkage map of human 9q34.1.Semantic proximity Read ↗

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.Semantic proximity Read ↗

Large deletion at the TSC1 locus in a family with tuberous sclerosis complex.Semantic proximity Read ↗

D10S681, a microsatellite polymorphism near the RET locus.Semantic proximity Read ↗

Three novel mutations of TSC1 gene in Chinese patients with tuberous sclerosis complex.Semantic proximity Read ↗

A novel missense mutation in the GTPase activating protein homology region of TSC2 in two large families with tuberous sclerosis complexSemantic proximity Read ↗

Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) gene.Semantic proximity Read ↗

Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex.Semantic proximity Read ↗

Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family.Semantic proximity Read ↗

Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.Semantic proximity Read ↗

TRPS1 codon 952 constitutes a mutational hot spot in trichorhinophalangeal syndrome type I and could be associated with intellectual disability.Semantic proximity Read ↗

[Mutation and polymorphism in exon 4 of tuberous sclerosis complex gene].Semantic proximity Read ↗

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