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Volumn 78, Issue 2, 1998, Pages 123-126

Duplication 6q22→qter: Definition of the phenotype

Author keywords

6q trisomy; Chromosome 6 duplication; Ebstein's malformation of tricuspid valve; Renal hypoplasia

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 6Q; CHROMOSOME DUPLICATION; CONGENITAL HEART DISEASE; DEVELOPMENTAL DISORDER; FEMALE; HEARING LOSS; HUMAN; KIDNEY HYPOPLASIA; MICROCEPHALY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; WEBBED NECK; CHROMOSOME 14; CHROMOSOME 6; GENE TRANSLOCATION; GENETICS; INFANT; MULTIPLE MALFORMATION SYNDROME;

EID: 0032580787     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980630)78:2<123::AID-AJMG5>3.0.CO;2-P     Document Type: Article
Times cited : (5)

References (12)
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  • 4
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  • 6
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  • 7
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  • 8
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    • Prenatal diagnosis of a de novo trisomy 6q22.2 → 6qter and monosomy 1pter-1p36.3: Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q
    • Kulharya AS, Carlin ME, Stettler WA, Huslig M, Kukolich MK, Garcia-Heras J (1997): Prenatal diagnosis of a de novo trisomy 6q22.2 → 6qter and monosomy 1pter-1p36.3: Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q. Clin Genet 51:115-117.
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  • 9
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    • Partial duplication of the long arm of chromosome 6: A clinically recognizable syndrome
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  • 11
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.