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CompleteSHOX deficiency causes Langer mesomelic dysplasia

✍ Scribed by Zinn, Andrew R. ;Wei, Fanglin ;Zhang, Ling ;Elder, Frederick F. ;Scott, Charles I. ;Marttila, Pia ;Ross, Judith L.


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
188 KB
Volume
110
Category
Article
ISSN
0148-7299

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Pseudodominant inheritance of Langer mes
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## Abstract We report the clinical and molecular analysis in a consanguineous family in which the skeletal dysplasias LΓ©ri‐Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD) both segregate. A newborn male and his mother, both with Langer mesomelic dysplasia, are described. A homozyg