A genetic etiology for DiGeorge syndrome: Consistent deletions and microdeletions of 22q11

American Journal of Human Genetics

Volumn 50, Issue 5, 1992, Pages 924-933

  Driscoll, D A ^a   Budarf, M L ^a   Emanuel, B S ^a  

^a HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CLINICAL ARTICLE; CYTOGENETICS; DIGEORGE SYNDROME; GENE DELETION; GENE MAPPING; HUMAN; HUMAN CELL; MOLECULAR GENETICS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

BLOTTING, SOUTHERN; CELL LINE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DNA PROBES; FEMALE; HUMAN; MALE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026750771     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)