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Volumn 34, Issue 6, 2000, Pages 72-74

16Q subtelomeric deletion in proband with congenital malformations and mental retardation

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 16; CONGENITAL MALFORMATION; FEMALE; GENE DELETION; GENETICS; HUMAN; KARYOTYPING; MENTAL DEFICIENCY; TELOMERE;

EID: 0034331250     PISSN: 05643783     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (9)
  • 4
    • 0006838454 scopus 로고
    • Microwave activation of fluorescence in situ hybridization: Novel method for rapid chromosome detection and analysis
    • Soloviev I. V., Yurov Yu. B., Vorsanova S. G., Malet P. Microwave activation of fluorescence in situ hybridization: novel method for rapid chromosome detection and analysis // Focus. 1994. - 16, N 4. - P. 115-116.
    • (1994) Focus , vol.16 , Issue.4 , pp. 115-116
    • Soloviev, I.V.1    Yurov, Yu.B.2    Vorsanova, S.G.3    Malet, P.4
  • 5
    • 0006771637 scopus 로고    scopus 로고
    • Identification and molecular-cytogenetic characterization of large subset of human plasmids, cosmids, PAC and YAC clones: The search of DNA probes for pre- And postnatal diagnosis
    • Soloviev I. V., Yurov Yu. B., Ioannou P., Georghion A., Hadjimarcou M., Patsalis P., Roizes G., Sharonin V. O., Kravets V. S., Vorsanova S. G. Identification and molecular-cytogenetic characterization of large subset of human plasmids, cosmids, PAC and YAC clones: the search of DNA probes for pre- and postnatal diagnosis // Ca. Pediat. - 1997. - 52, N 7. - P. 529-538.
    • (1997) Ca. Pediat. , vol.52 , Issue.7 , pp. 529-538
    • Soloviev, I.V.1    Yurov, Yu.B.2    Ioannou, P.3    Georghion, A.4    Hadjimarcou, M.5    Patsalis, P.6    Roizes, G.7    Sharonin, V.O.8    Kravets, V.S.9    Vorsanova, S.G.10
  • 6
    • 0042827000 scopus 로고    scopus 로고
    • DNA probes for pre- and postnatal diagnosis of chromosomal anomalies: A collection for FISH analysis
    • Yurov Yu. B., Soloviev I. V., Vorsanova S. G., Alexandrov I. A., Sharonin V. O., Monachov V. V. DNA probes for pre- and postnatal diagnosis of chromosomal anomalies: a collection for FISH analysis // Cš. Pediat. - 1997. - 52, N 7. - P. 550-554.
    • (1997) Cš. Pediat. , vol.52 , Issue.7 , pp. 550-554
    • Yurov, Yu.B.1    Soloviev, I.V.2    Vorsanova, S.G.3    Alexandrov, I.A.4    Sharonin, V.O.5    Monachov, V.V.6
  • 8
    • 0021869151 scopus 로고
    • Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters
    • Hoo J. J., Lowry R. B., Lin C. C., Haslam R. H. A. Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters // Clin. Genet. - 1985. - 27. - P. 420-435.
    • (1985) Clin. Genet. , vol.27 , pp. 420-435
    • Hoo, J.J.1    Lowry, R.B.2    Lin, C.C.3    Haslam, R.H.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.