A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

Nature Genetics

Volumn 13, Issue 4, 1996, Pages 458-460

  Daw, S C M ^a   Taylor, C ^a   Kraman, M ^a   Call, K ^a   Mao, J I ^a   Schuffenhauer, S ^a   Meitinger, T ^a   Lipson, T ^a   Goodship, J ^a   Scambler, P ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CELLULAR IMMUNODEFICIENCY; CHROMOSOME 10P; CHROMOSOME DELETION; CLINICAL ARTICLE; DIGEORGE SYNDROME; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC MARKER; HUMAN; HYPOPARATHYROIDISM; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 10; DIGEORGE SYNDROME; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; SYNDROME;

EID: 15844403609     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0896-458     Document Type: Article

References (0)