Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: Genomic organization and deletion endpoint analysis

Human Molecular Genetics

Volumn 9, Issue 4, 2000, Pages 489-501

  Shaikh, Tamim H ^a   Kurahashi, Hiroki ^a   Saitta, Sulagna C ^a   O'Hare, Anna Mizrahy ^a   Hu, Ping ^c   Roe, Bruce A ^c   Driscoll, Deborah A ^a,b   McDonald McGinn, Donna M ^a   Zackai, Elaine H ^a,b   Budarf, Marcia L ^a,b   Emanuel, Beverly S ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c UNIVERSITY OF OKLAHOMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA;

ANIMAL CELL; ARTICLE; CHROMOSOME 22Q; CONTROLLED STUDY; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE NUMBER; HEMIZYGOSITY; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; MONKEY; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS; SEQUENCE HOMOLOGY; SOUTHERN BLOTTING; VELOCARDIOFACIAL SYNDROME;

ANIMALIA; CERCOPITHECIDAE; PRIMATES;

EID: 0034161932     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.4.489     Document Type: Article

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