Report of a further family with dominant deafness-onychodystrophy (DDOD) syndrome

American Journal of Medical Genetics, Part A

Volumn 155, Issue 10, 2011, Pages 2512-2515

  White, Susan M ^a,b   Fahey, Michael ^c  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c MONASH UNIVERSITY   (Australia)

Author keywords

Deafness; Dominant deafness onychodystrophy (DDOD) syndrome; Onychodystrophy

Indexed keywords

ADULT; AGED; ARTICLE; AUTOPSY; AUTOSOMAL DOMINANT DISORDER; BRACHYDACTYLY; BRONCHITIS; CASE REPORT; CONGENITAL RUBELLA SYNDROME; DOMINANT DEAFNESS ONYCHODYSTROPHY SYNDROME; EPILEPSY; FACE DYSMORPHIA; FEMALE; FOOT RADIOGRAPHY; HAND RADIOGRAPHY; HUMAN; HYPOTELORISM; INFANT; MALE; MYOPIA; NAIL APLASIA; NAIL DYSPLASIA; NAIL DYSTROPHY; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SKIN APLASIA; SUDDEN INFANT DEATH SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; FEMALE; GENES, DOMINANT; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; MALE; NAILS, MALFORMED; PEDIGREE; SYNDROME;

EID: 80053124868     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34184     Document Type: Article

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