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Volumn 143, Issue 24, 2007, Pages 3302-3308

A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients

Author keywords

Chromosomal microarray; DiGeorge syndrome; Opitz GBBB; Velocardiofacial syndrome

Indexed keywords

CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL EXAMINATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONFERENCE PAPER; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE MUTATION; HUMAN; KARYOTYPE; MALE; OPITZ SYNDROME; PHENOTYPE; PRIORITY JOURNAL; VELOCARDIOFACIAL SYNDROME;

EID: 37249043719     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32025     Document Type: Conference Paper
Times cited : (9)

References (26)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.