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Volumn 61, Issue 6, 1997, Pages 485-490

Molecular characterization of isochromosomes of xq

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CENTROMERE; CHROMOSOME XQ; CLINICAL ARTICLE; FEMALE; HUMAN; HUMAN CELL; ISOCHROMOSOME; PARENTAL AGE; PRIORITY JOURNAL; X CHROMOSOME;

EID: 0031408984     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480097006519     Document Type: Article
Times cited : (32)

References (13)
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  • 3
    • 0023481818 scopus 로고
    • Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences
    • CALLEN, D. F., MULLEY, J. C., BAKER, E. G. & SUTHERLAND, G. R. (1987). Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences. Hum. Genet. 77, 236-240.
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    • Callen, D.F.1    Mulley, J.C.2    Baker, E.G.3    Sutherland, G.R.4
  • 4
    • 0023715084 scopus 로고
    • Molecular studies of the parental origin and nature of human X isochromosomes
    • HARBISON, M., HASSOLD, T., KOBRYN, C. & JACOBS, P. A. (1988). Molecular studies of the parental origin and nature of human X isochromosomes. Cytogenet. Cell Genet. 47, 217-222.
    • (1988) Cytogenet. Cell Genet. , vol.47 , pp. 217-222
    • Harbison, M.1    Hassold, T.2    Kobryn, C.3    Jacobs, P.A.4
  • 5
    • 0020634258 scopus 로고
    • The distribution of chromosomal genotypes associated with Turner's syndrome: Livebirth prevalence rates and evidence of diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism
    • HOOK, E. B. & WARBURTON, D. (1983). The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence of diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism. Hum. Genet. 64, 24-27.
    • (1983) Hum. Genet. , vol.64 , pp. 24-27
    • Hook, E.B.1    Warburton, D.2
  • 7
    • 0026042198 scopus 로고
    • A molecular study of X isochromosomes: Parental orgin, centromeric structure, and mechanisms of formation
    • LORDA-SANCHEZ, I., BINKERT, F., MAECHLER, M. & SCHINZEL, A. (1991). A molecular study of X isochromosomes: parental orgin, centromeric structure, and mechanisms of formation. Am. J. Hum. Genet. 49, 1034-1040.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 1034-1040
    • Lorda-Sanchez, I.1    Binkert, F.2    Maechler, M.3    Schinzel, A.4
  • 8
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • MILLER, S. A., DYKES, D. D. & POLESKY, H. F. (1988). A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16, 1215.
    • (1988) Nucleic Acids Res. , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 10
    • 0015246254 scopus 로고
    • A rapid banding technique for human chromosomes
    • SEABRIGHT, M. (1971). A rapid banding technique for human chromosomes. Lancet ii, 971-972.
    • (1971) Lancet ii , pp. 971-972
    • Seabright, M.1
  • 11
    • 0025160230 scopus 로고
    • Pericentromerie structure of human X 'isochromosomes': Evidence for molecular heterogeneity
    • SHARP, C. B., BEDFORD, H. M. & WILLARD, H. F. (1990). Pericentromerie structure of human X 'isochromosomes': evidence for molecular heterogeneity. Hum. Genet. 85, 330-336.
    • (1990) Hum. Genet. , vol.85 , pp. 330-336
    • Sharp, C.B.1    Bedford, H.M.2    Willard, H.F.3
  • 12
    • 0017126281 scopus 로고
    • Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy
    • WILLARD, H. F. & LATT, S.A. (1976). Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. Am. J. Hum. Genet. 13, 213-227.
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    • Willard, H.F.1    Latt, S.A.2
  • 13
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    • Molecular definition of breakpoints associated with human Xq isochromosomes: Implications for mechanisms of formation
    • WOLFF, D. J., MILLER, A. P., VAN DYKE, D. L., SCHWARTZ, S. & WILLARD, H. F. (1996). Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation. Am. J. Hum. Genet. 58, 154-160.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.