Report of a third family with Oliver syndrome [2]

American Journal of Medical Genetics, Part A

Volumn 139 A, Issue 2, 2005, Pages 159-161

  Salpietro, Carmelo Damiano ^a   Briuglia, Silvana ^a   Bertuccio, Graziella ^a   Rigoli, Luciana ^a   Mingarelli, Rita ^b   Dallapiccola, Bruno ^b  

^a UNIVERSITY OF MESSINA   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANAMNESIS; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHROMOSOME DISORDER; CLINICAL FEATURE; CONGENITAL MALFORMATION; EPILEPSY; FEMALE; GENETIC ANALYSIS; HUMAN; LABORATORY TEST; LETTER; MALE; MALFORMATION SYNDROME; MENTAL DEFICIENCY; OLIVER SYNDROME; POLYDACTYLY; PRIORITY JOURNAL; GENETIC COUNSELING; GENETICS; PATHOPHYSIOLOGY; RADIOGRAPHY; SYNDROME;

ADOLESCENT; ADULT; FEMALE; GENETIC COUNSELING; HUMANS; MALE; POLYDACTYLY; SYNDROME;

EID: 33645848768     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.30999     Document Type: Letter

References (4)

1. Castilla EE, Lugarinho R, da Graca Dutra M, Salgado LJ. 1998. Associated anomalies in individuals with polydactyly. Am J Med Genet 80:459-465.
2. Gorlin RJ, Cohen MM, Hennekam RCM. 2001. Syndromes of the head and neck. New York: Oxford University Press.
3. Oliver CP. 1940. Recessive polydactylism associated with mental deficiency. J Hered 31:365-367.
4. Stevenson RE, Wilkes G. 1983. Polydactyly and mental retardation in siblings. Proc Greenwood Genet Center 2:20-22.