Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a population-based sample of infants with cleft palate

American Journal of Medical Genetics, Part A

Volumn 143, Issue 2, 2007, Pages 129-134

  Sivertsen, Åse ^a   Lie, Rolv Terje ^a   Wilcox, Allen J ^b   Åbyholm, Frank ^c   Vindenes, Halvard ^d   Haukanes, Bjørn Ivar ^d   Houge, Gunnar ^d  

^a UNIVERSITY OF BERGEN   (Norway)

^b NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES   (United States)

^c OSLO UNIVERSITY HOSPITAL   (Norway)

^d HAUKELAND UNIVERSITY HOSPITAL   (Norway)

Author keywords

22q11.2 deletions; 22q11.2 duplications; Cleft palate; del22q11 syndrome; DiGeorge syndrome

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLEFT PALATE; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; DIGEORGE SYNDROME; DNA DETERMINATION; DNA PROBE; GENE AMPLIFICATION; GENE NUMBER; GENETIC ASSOCIATION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; NEWBORN; NORWAY; POPULATION GENETICS; PREVALENCE; PRIORITY JOURNAL;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CLEFT PALATE; DIGEORGE SYNDROME; GENE DOSAGE; GENE DUPLICATION; HUMANS; INFANT; NORWAY; PREVALENCE;

EID: 33845966776     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31445     Document Type: Article

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