Literature DB >> 9660051

Limb development: molecular dysmorphology is at hand!

J W Innis1, D P Mortlock.   

Abstract

We present a review of limb development integrating current molecular information and selected genetic disorders to illustrate the advances made in this field over the last few years. With this knowledge, clinical geneticists can now begin to consider molecular mechanisms and pathways when investigating patients with limb malformation syndromes.

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Year:  1998        PMID： 9660051     DOI： 10.1111/j.1399-0004.1998.tb02744.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  3 in total

1.  Why study human limb malformations?

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

2.  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

3.  p63 Coordinates anogenital modeling and epithelial cell differentiation in the developing female urogenital tract.

Authors:  Tan A Ince; Aida P Cviko; Bradley J Quade; Annie Yang; Frank D McKeon; George L Mutter; Christopher P Crum
Journal:  Am J Pathol       Date:  2002-10       Impact factor: 4.307
  3 in total

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