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Volumn 95, Issue 1, 2000, Pages 28-35

Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements

Author keywords

Complex chromosome rearrangement; Cryptic rearrangement; Fluorescence in situ hybridization; Townes Brocks syndrome

Indexed keywords

ANUS ATRESIA; ARTICLE; ATTENTION DEFICIT DISORDER; CASE REPORT; CHROMOSOME 10; CHROMOSOME 11; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 2; CHROMOSOME 3; CHROMOSOME 3P; CHROMOSOME 5; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CYTOGENETICS; DIAGNOSTIC VALUE; DNA DETERMINATION; EAR MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC DISORDER; GENITAL SYSTEM; HUMAN; INFANT; KARYOTYPE; LEARNING DISORDER; MALE; OBESITY; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SCHOOL CHILD; TOWNES BROCKS SYNDROME;

EID: 0034613963     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20001106)95:1<28::AID-AJMG7>3.0.CO;2-C     Document Type: Article
Times cited : (9)

References (18)
  • 13
    • 0002087696 scopus 로고
    • Preferential paternal origin of de novo structural chromosome rearrangements
    • Daniel A, editor. The cytogenetics of mammalian autosomal rearrangements. New York: Alan R Liss. p
    • (1988) , pp. 583-599
    • Olson, S.B.1    Magenis, R.E.2
  • 18
    • 0028813216 scopus 로고
    • A familial 'balanced' 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings
    • (1995) Am J Hum Genet , vol.56 , pp. 302-309
    • Wagstaff, J.1    Hemann, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.