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Volumn 155, Issue 12, 2011, Pages 3071-3074

A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)

Author keywords

Array CGH with exonic coverage; Diepoxybutane; FANCB protein; Fanconi anemia; Mitomycin; Oligonucleotide array CGH; VACTERL

Indexed keywords

ANUS DISEASE; ARTICLE; BONE EXAMINATION; CASE REPORT; CHROMOSOME BREAKAGE; CHROMOSOME LOSS; CHROMOSOME XP; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASE ASSOCIATION; DISEASE SEVERITY; ECHOCARDIOGRAPHY; ENDOTRACHEAL INTUBATION; ESOPHAGUS ATRESIA; ESOPHAGUS SURGERY; FANCONI ANEMIA; FANCONI ANEMIA COMPLEMENTATION GROUP B GENE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE IDENTIFICATION; GENETIC ASSOCIATION; HEART ATRIUM SEPTUM DEFECT; HEART SURGERY; HUMAN; KIDNEY MALFORMATION; LIMB MALFORMATION; MALE; MALFORMATION SYNDROME; MUTATOR GENE; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATENT DUCTUS ARTERIOSUS; PRIORITY JOURNAL; THROMBOCYTOPENIA; TRACHEOESOPHAGEAL FISTULA; TRACHEOSTOMY; VERTEBRA MALFORMATION;

EID: 81955164128     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34296     Document Type: Article
Times cited : (11)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.