Cytogenetic findings in a prospective series of patients with DiGeorge anomaly

American Journal of Human Genetics

Volumn 43, Issue 5, 1988, Pages 605-611

  Greenberg, F ^a   Elder, F F B ^a   Haffner, P ^a   Northrup, H ^a   Ledbetter, D H ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 10P; CHROMOSOME 22Q; CHROMOSOME DELETION 22; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CYTOCHEMISTRY; CYTOLOGY; DIGEORGE SYNDROME; GENETIC COUNSELING; GENETIC RISK; HEREDITY; HUMAN; PARTIAL MONOSOMY 10; PARTIAL MONOSOMY 22; PRIORITY JOURNAL;

CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HUMAN; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; KARYOTYPING; MALE; PROSPECTIVE STUDIES; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0023815540     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)