Literature DB >> 10951468

Acampomelic campomelic dysplasia with SOX9 mutation.

M K Thong1, G Scherer, K Kozlowski, E Haan, L Morris.   

Abstract

Acampomelic campomelic dysplasia is a rare clinical variant of the more commonly encountered campomelic dysplasia (CMD1), characterized by absence of long bone curvature (acampomelia). We present a patient with acampomelic CMD1 with a de novo SOX9 missense mutation and report his clinical course to age one year, thereby contributing to genotype-phenotype correlation in CMD1. 2000. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10951468

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

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4.  Acampomelic form of campomelic dysplasia with SOX9 missense mutation.

Authors:  Hariharan Gopakumar; Andrea Superti-Furga; Sheila Unger; Gerd Scherer; P K Rajiv; Sheela Nampoothiri
Journal:  Indian J Pediatr       Date:  2013-04-07       Impact factor: 1.967

5.  Clinical and molecular characterization of a Brazilian cohort of campomelic dysplasia patients, and identification of seven new SOX9 mutations.

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Review 6.  Diverse Regulation but Conserved Function: SOX9 in Vertebrate Sex Determination.

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  6 in total

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