CDKN1C mutations and genital anomalies

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 1, 2012, Pages 265-

  Welsh, Holly I ^a   Stockley, Tracy L ^b,c   Parkinson, Nicole ^b,c   Ardinger, Holly H ^a  

^a CHILDREN S MERCY HOSPITAL   (United States)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CDKN1C GENE; EAR MALFORMATION; GENE; GENE MUTATION; GENE SEQUENCE; HUMAN; HYPOSPADIAS; INGUINAL HERNIA; INHERITANCE; LETTER; MALE; MALE GENITAL TRACT MALFORMATION; METHYLATION; OMPHALOCELE; PRIORITY JOURNAL;

BECKWITH-WIEDEMANN SYNDROME; CYCLIN-DEPENDENT KINASE INHIBITOR P57; GENETIC ASSOCIATION STUDIES; GENITALIA; HUMANS; INFANT, NEWBORN; MALE; MUTATION; SEQUENCE ANALYSIS;

EID: 84355161395     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34388     Document Type: Letter

References (3)

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