Conradi-Hünermann-Happle syndrome with unilateral distribution;Syndrome de Conradi-Hünermann-Happle de disposition unilatérale

Annales de Dermatologie et de Venereologie

Volumn 137, Issue 1, 2010, Pages 44-47

  Hello, M ^a   David, A ^b   Barbarot, S ^a  

^a CLINIQUE DERMATOLOGIQUE   (France)

^b NANTES UNIVERSITY HOSPITAL   (France)

Author keywords

Conradi H nermann Happle syndrome; EBP gene; Genodermatosis; Punctuate epiphyseal calcifications; X linked dominant chondrodysplasia punctata

Indexed keywords

3 BETA HYDROXYSTEROID ISOMERASE; ISOMERASE; UNCLASSIFIED DRUG;

ARTICLE; CALCIFYING CHONDRODYSTROPHY; CASE REPORT; ERYTHEMA; FEMALE; GENE MUTATION; HUMAN; MOSAICISM; NEWBORN; X CHROMOSOME INACTIVATION;

CHONDRODYSPLASIA PUNCTATA; FEMALE; HUMANS; INFANT, NEWBORN; MORPHOGENESIS; STEROID ISOMERASES; X CHROMOSOME INACTIVATION;

EID: 74149084613     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.annder.2009.11.006     Document Type: Article

References (11)

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