Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome

American Journal of Human Genetics

Volumn 65, Issue 3, 1999, Pages 779-783

  Brzustowicz, L M ^a,b,e   Farrell, S ^c   Khan, M B ^a   Weksberg, R ^d  

^a RUTGERS UNIVERSITY   (United States)

^b RUTGERS NEW JERSEY MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF TORONTO   (Canada)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e RUTGERS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XP; FEMALE; GENE DISRUPTION; GENE LOCATION; GENE LOCUS; GENOTYPE; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; SIMPSON GOLABI BEHMEL SYNDROME; TANDEM REPEAT;

HYDROPS;

EID: 0033358672     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302527     Document Type: Article

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