Severe Phenotype of X-linked Dominant Chondrodysplasia Punctata

Overview

Journal Clin Case Rep

Date 2017 Sep 8

PMID 28878897

Citations 1

Authors

Nadirah Damseh

Karen Chong

Christian Marshall

Lisa Kratz

Ronni Teitelbaum

Patrick Shannon

Peter Kannu

Affiliations

Soon will be listed here.

Abstract

A prenatally ascertained case representing the more severe end of the X-linked dominant chondrodysplasia punctata (CDPX2).

Citing Articles

Severe phenotype of X-linked dominant chondrodysplasia punctata.

Damseh N, Chong K, Marshall C, Kratz L, Teitelbaum R, Shannon P Clin Case Rep. 2017; 5(9):1435-1437.

PMID: 28878897 PMC: 5582310. DOI: 10.1002/ccr3.1008.

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Damseh N, Chong K, Marshall C, Kratz L, Teitelbaum R, Shannon P . Severe phenotype of X-linked dominant chondrodysplasia punctata. Clin Case Rep. 2017; 5(9):1435-1437. PMC: 5582310. DOI: 10.1002/ccr3.1008. View

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