Literature DB >> 10498937

Genetics of limb anomalies in humans.

S Manouvrier-Hanu1, M Holder-Espinasse, S Lyonnet.   

Abstract

The limbs have an essential function in all vertebrates. In animals, the key genes that are involved in the growth and patterning of the limb buds, and of the development of the complex extremities, have been identified and their interactions recognized. Aided by these discoveries, human genetics has also been able to identify, or at least localize, certain genes responsible for anomalies of the limbs. These malformations are isolated or associated with anomalies of other developmental fields, according to the expression domain of the gene involved. Increasing knowledge of the embryology and genes involved has lead to a regrouping of malformation manifestations in genetics terms. Clear genotype-phenotype correlations are difficult to establish owing to the interlinking network of genetic signals underlying limb development.

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Year:  1999        PMID: 10498937     DOI: 10.1016/s0168-9525(99)01823-5

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  13 in total

1.  Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

Authors:  K Bosse; R C Betz; Y A Lee; T F Wienker; A Reis; H Kleen; P Propping; S Cichon; M M Nöthen
Journal:  Am J Hum Genet       Date:  2000-06-30       Impact factor: 11.025

2.  Why study human limb malformations?

Authors:  Andrew O M Wilkie
Journal:  J Anat       Date:  2003-01       Impact factor: 2.610

3.  Sequence characterization and promoter identification of porcine APC10 gene.

Authors:  W B He; Z W Wang; Y Li; Z L Tang; S L Yang; Y L Mu; K M Peng; K Li
Journal:  Mol Biol Rep       Date:  2010-03-16       Impact factor: 2.316

4.  Association between selected folate pathway polymorphisms and nonsyndromic limb reduction defects: a case-parental analysis.

Authors:  Mario A Cleves; Charlotte A Hobbs; Weizhi Zhao; Patrycja A Krakowiak; Stewart L MacLeod
Journal:  Paediatr Perinat Epidemiol       Date:  2011-01-04       Impact factor: 3.980

5.  Oligosyndactylism mice have an inversion of chromosome 8.

Authors:  Thomas L Wise; Dimitrina D Pravtcheva
Journal:  Genetics       Date:  2004-12       Impact factor: 4.562

6.  A minimalist approach to gene mapping: locating the gene for acheiropodia, by homozygosity analysis.

Authors:  M A Escamilla; M C DeMille; E Benavides; E Roche; L Almasy; S Pittman; J Hauser; D F Lew; N B Freimer; M R Whittle
Journal:  Am J Hum Genet       Date:  2000-04-25       Impact factor: 11.025

7.  Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.

Authors:  G C Schwabe; S Tinschert; C Buschow; P Meinecke; G Wolff; G Gillessen-Kaesbach; M Oldridge; A O Wilkie; R Kömec; S Mundlos
Journal:  Am J Hum Genet       Date:  2000-09-12       Impact factor: 11.025

8.  Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genes.

Authors:  Thomas J Carney; Natália Martins Feitosa; Carmen Sonntag; Krasimir Slanchev; Johannes Kluger; Daiji Kiyozumi; Jan M Gebauer; Jared Coffin Talbot; Charles B Kimmel; Kiyotoshi Sekiguchi; Raimund Wagener; Heinz Schwarz; Phillip W Ingham; Matthias Hammerschmidt
Journal:  PLoS Genet       Date:  2010-04-15       Impact factor: 5.917

9.  The epidemiology, genetics and future management of syndactyly.

Authors:  D Jordan; S Hindocha; M Dhital; M Saleh; W Khan
Journal:  Open Orthop J       Date:  2012-03-23

10.  Birth prevalence for congenital limb defects in the northern Netherlands: a 30-year population-based study.

Authors:  Ecaterina Vasluian; Corry K van der Sluis; Anthonie J van Essen; Jorieke E H Bergman; Pieter U Dijkstra; Heleen A Reinders-Messelink; Hermien E K de Walle
Journal:  BMC Musculoskelet Disord       Date:  2013-11-16       Impact factor: 2.362

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