Bloom syndrome: A single complementation group defines patients of diverse ethnic origin

American Journal of Human Genetics

Volumn 42, Issue 6, 1988, Pages 816-824

  Weksberg, R ^a   Smith, C ^a   Anson Cartwright, L ^a   Maloney, K ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOM SYNDROME; CELL CULTURE; CYTOLOGY; ETHNIC GROUP; ETHNIC OR RACIAL ASPECTS; GENETIC HETEROGENEITY; HEREDITY; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; SISTER CHROMATID EXCHANGE;

ADOLESCENT; ADULT; BLOOM SYNDROME; CELL FUSION; CELL LINE; CHILD; CHILD, PRESCHOOL; GENETIC COMPLEMENTATION TEST; GENETIC MARKERS; HUMAN; INFANT; KARYOTYPING; SISTER CHROMATID EXCHANGE; SUPPORT, NON-U.S. GOV'T; VARIATION (GENETICS);

EID: 0023943610     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)