Johnson-McMillin syndrome: Report of a new case with novel features

Birth Defects Research Part A - Clinical and Molecular Teratology

Volumn 73, Issue 9, 2005, Pages 638-641

  Cushman, Lisa J ^a   Torres Martinez, Wilfredo ^a   Weaver, David D ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

AADH syndrome; Alopecia; Autosomal dominant inheritance; Birth defects; Branchial arch; Johnson neuroectodermal syndrome; Johnson Mcmillin syndrome

Indexed keywords

ALOPECIA; ANOSMIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CLINICAL FEATURE; CONDUCTION DEAFNESS; DEVELOPMENTAL DISORDER; DIFFERENTIAL DIAGNOSIS; EAR MALFORMATION; EMBRYO DEVELOPMENT; FEMALE; HUMAN; HYPERGONADOTROPIC HYPOGONADISM; JOHNSON MCMILLIN SYNDROME; MULTIPLE MALFORMATION SYNDROME; NEURECTODERM; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ALOPECIA; CHILD, PRESCHOOL; EAR, EXTERNAL; FACIAL ASYMMETRY; FEMALE; GENES, DOMINANT; HEARING LOSS, CONDUCTIVE; HUMANS; MENTAL RETARDATION; NEUROCUTANEOUS SYNDROMES; SYNDROME;

EID: 26444493603     PISSN: 15420752     EISSN: None     Source Type: Journal    
DOI: 10.1002/bdra.20178     Document Type: Article

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