home > bioproject > PRJNA74829
identifier PRJNA74829
type bioproject
sameAs
sra-study  SRP003269
organism Homo sapiens
title Genetic Analysis of Limb Malformation Disorders: Freeman Sheldon Exome Sequencing
description The overall goal of this project is to investigate the etiology and pathogenesis of malformations (i.e., birth defects) of the limb, concentrating on abnormalities of limb patterning such as limb deficiency/duplications and multiple congenital contractures. The exome sequences of four unrelated individuals were obtained by massively parallel DNA sequencing. The three individuals were affected with Freeman Sheldon syndrome (OMIM:193700).
data type Phenotype or Genotype
organization
publication
Targeted capture and massively parallel sequencing of 12 human exomes.
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