Concurrent microdeletion and duplication of 22q11.2

Clinical Genetics

Volumn 74, Issue 1, 2008, Pages 61-67

  Blennow, Elisabeth ^a,b   Lagerstedt, K ^a   Malmgren, S ^a   Sahlen S ^a   Schoumans, J ^a   Anderlid, B M ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

22q11; Array CGH; Fluorescent in situ hybridization; Microdeletion; Microduplication; Multiplex ligation dependent probe amplification

Indexed keywords

ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME MAP; CHROMOSOME MOSAICISM; CHROMOSOME REARRANGEMENT; COMORBIDITY; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; HUMAN; LEARNING DISORDER; PALATOPHARYNGEAL INCOMPETENCE; PERIPHERAL LYMPHOCYTE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; RECURRENT INFECTION; SOCIAL PROBLEM; VELOCARDIOFACIAL SYNDROME;

ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; GENE DUPLICATION; HUMANS; MOSAICISM; NUCLEIC ACID HYBRIDIZATION;

EID: 45149102094     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2008.01008.x     Document Type: Article

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