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Volumn 80, Issue 5, 1998, Pages 448-453

Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6

Author keywords

Chromosome translocation; Dandy Walker anomaly; Deletion 5qter; Deletion 6qter; Duplication 5qter; Duplication 6qter; FISH; Microcephaly; Retinitis pigmentosa

Indexed keywords

ARTICLE; CHROMOSOME TRANSLOCATION 5; CHROMOSOME TRANSLOCATION 6; CLINICAL ARTICLE; CYTOGENETICS; FAMILIAL DISEASE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; MENTAL DEFICIENCY; MICROCEPHALY; PEDIGREE; PRIORITY JOURNAL; PROGENY;

EID: 0032545202     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19981228)80:5<448::AID-AJMG3>3.0.CO;2-Q     Document Type: Article
Times cited : (11)

References (15)
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  • 4
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  • 7
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    • A distinct multiple congenital syndrome associated with distal 5q deletion (q35.1qter)
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  • 8
    • 0023134292 scopus 로고
    • Clinical manifestations of trisomy 5q
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  • 10
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  • 12
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    • Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting
    • Rubstov N, Senger G, Kuzcera H, Neumann A, Kelbova C, Junker K, Beensen V, Claussen U (1996): Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting. Hum Genet 97:705-709.
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  • 15
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    • Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.