Waardenburg syndrome: Variable phenotypic expression in monozygotic twins

Clinical Dysmorphology

Volumn 7, Issue 1, 1998, Pages 77-78

  Suyugül, Zuhal ^a,b   Tüysüz, Beyhan ^a,b   Tükenmez, Faruk ^a,b   Basaran, Müjdat ^a,b   Cenani, Asim ^a,b  

^a ISTANBUL UNIVERSITY   (Turkey)

^b MARMARA UNIVERSITY   (Turkey)

Author keywords

Monozygotic twins; Waardenburg syndrome

Indexed keywords

CASE REPORT; CONGENITAL MALFORMATION; DUODENUM; FACIES; FEMALE; GENETICS; HUMAN; INFANT; LETTER; MONOZYGOTIC TWINS; PATHOLOGY; PHENOTYPE; TWINS; WAARDENBURG SYNDROME;

DISEASES IN TWINS; DUODENUM; FACIES; FEMALE; HUMANS; INFANT; PHENOTYPE; TWINS, MONOZYGOTIC; WAARDENBURG'S SYNDROME;

EID: 0031613097     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199801000-00017     Document Type: Article

References (3)

1. Baldwin CT, Hoth CF, Macina RA et al. (1996). Mutations in PAX3 that cause Waardenburg syndrome Type I: ten new mutations and review of the literature. Am J Med Genet 58:115-122.
2. Reynolds JE, Meyer JM, Landa B et al. (1995). Analysis of variability of clinical manifestations in Waardenburg syndrome. Am J Med Genet 57:540-547.
3. Silva EO (1991). Waardenburg I syndrome: a clinical and genetic study of two large Brazilian kindreds, and literature review. Am J Med Genet 40:65-74.