Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome

Genomics

Volumn 10, Issue 1, 1991, Pages 201-206

  Scambler, Peter J ^a   Carey, Alisoun H ^a   Wyse, Richard K H ^b   Roach, Sherry ^a   Dumanski, Jan P ^c   Nordenskjold, Magnus ^c   Williamson, Robert ^c  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c KAROLINSKA INSTITUTE   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CELL LINE; CHROMOSOME 22Q; CHROMOSOME DELETION; DIGEORGE SYNDROME; DNA PROBE; HUMAN; HUMAN CELL;

CELL LINE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DENSITOMETRY; DIGEORGE SYNDROME; GENETIC MARKERS; HUMAN; NUCLEIC ACID HYBRIDIZATION; PHENOTYPE; SUPPORT, NON-U.S. GOV'T;

EID: 0025796855     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/0888-7543(91)90501-5     Document Type: Article

References (27)

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