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Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene

JCRPE Journal of Clinical Research in Pediatric Endocrinology - Turkey
doi 10.4274/jcrpe.1835
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Abstract

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Categories
Child HealthEndocrinologyPerinatologyPediatricsMetabolismDiabetes
Date

March 5, 2015

Authors
Abdullah ÇimSalih CoşkunOrhan GörükmezHatice YükselÜnal UlucaErminia Di PietroFrançois PlourdeNancy Elise Braverman
Publisher

Galenos Yayinevi


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