메뉴 건너뛰기




Volumn 104, Issue 4, 1999, Pages 345-349

Analysis of sex chromosome aneuploidy in sperm from fathers of Turner syndrome patients

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME POLYMORPHISM; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MALE; MEIOSIS; MOSAICISM; PARENTHOOD; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEMEN ANALYSIS; SEX CHROMOSOME; STATISTICAL ANALYSIS; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME;

EID: 18844463311     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050964     Document Type: Article
Times cited : (66)

References (30)
  • 1
    • 0032231320 scopus 로고    scopus 로고
    • Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21 in a population with a high prevalence of Down's syndrome. Increased incidence in cases of paternal origin
    • Blanco J, Gabau E, Gómez D, Baena N, Guitart M, Egozcue J, Vidal F (1998) Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21 in a population with a high prevalence of Down's syndrome. Increased incidence in cases of paternal origin. Am J Hum Genet 63:1067-1072
    • (1998) Am J Hum Genet , vol.63 , pp. 1067-1072
    • Blanco, J.1    Gabau, E.2    Gómez, D.3    Baena, N.4    Guitart, M.5    Egozcue, J.6    Vidal, F.7
  • 2
    • 0343091493 scopus 로고    scopus 로고
    • Numerical abnormalities in spermatozoa of aged men by multicolor FISH
    • Bosch M, Egozcue J, Templado C (1998) Numerical abnormalities in spermatozoa of aged men by multicolor FISH. Cytogenet Cell Genet 81:149
    • (1998) Cytogenet Cell Genet , vol.81 , pp. 149
    • Bosch, M.1    Egozcue, J.2    Templado, C.3
  • 4
  • 5
    • 0031181612 scopus 로고    scopus 로고
    • Detection of chromosomes and estimation of aneuploidy in human spermatozoa using fluorescence in-situ hybridization
    • Downie SD, Flaherty SP, Matthews CD (1997a) Detection of chromosomes and estimation of aneuploidy in human spermatozoa using fluorescence in-situ hybridization. Mol Hum Reprod 3:585-598
    • (1997) Mol Hum Reprod , vol.3 , pp. 585-598
    • Downie, S.D.1    Flaherty, S.P.2    Matthews, C.D.3
  • 6
    • 0031230287 scopus 로고    scopus 로고
    • Estimation of aneuploidy for chromosomes 3, 7, 16, X and Y in spermatozoa from 10 normospermic men using fluorescence in situ hybridization
    • Downie SD, Flaherty SP, Swann NJ, Matthews CD (1997b) Estimation of aneuploidy for chromosomes 3, 7, 16, X and Y in spermatozoa from 10 normospermic men using fluorescence in situ hybridization. Mol Hum Reprod 3:815-819
    • (1997) Mol Hum Reprod , vol.3 , pp. 815-819
    • Downie, S.D.1    Flaherty, S.P.2    Swann, N.J.3    Matthews, C.D.4
  • 7
    • 0031410184 scopus 로고    scopus 로고
    • Chromosome estudies in human sperm nuclei using fluorescence in-situ hybridization (FISH)
    • Egozcue J, Blanco J, Vidai F (1997) Chromosome estudies in human sperm nuclei using fluorescence in-situ hybridization (FISH). Hum Reprod Update 3:441-452
    • (1997) Hum Reprod Update , vol.3 , pp. 441-452
    • Egozcue, J.1    Blanco, J.2    Vidai, F.3
  • 8
    • 0025968910 scopus 로고
    • Rapid detection of CA polymorphisms in cloned DNA: Application to the 5' region of the dystrophin gene
    • Feener CA, Boyce FM, Kunkel LM (1991) Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene. Am J Hum Genet 48:621-627
    • (1991) Am J Hum Genet , vol.48 , pp. 621-627
    • Feener, C.A.1    Boyce, F.M.2    Kunkel, L.M.3
  • 10
    • 0030840912 scopus 로고    scopus 로고
    • Analysis of structural and numerical chromosome abnormalities in sperm from normal men and carriers of constitutional chromosome aberrations
    • Guttenbach M, Engel W, Schmid M (1997) Analysis of structural and numerical chromosome abnormalities in sperm from normal men and carriers of constitutional chromosome aberrations. A review. Hum Genet 100:1-21
    • (1997) A Review. Hum Genet , vol.100 , pp. 1-21
    • Guttenbach, M.1    Engel, W.2    Schmid, M.3
  • 11
    • 0022395534 scopus 로고
    • Determination of the parental origin of sex chromosome monosomy using restriction fragment length polymorphisms
    • HassoldT, Kumlin E, Takaesu N, Leppert M (1985) Determination of the parental origin of sex chromosome monosomy using restriction fragment length polymorphisms. Am J Hum Genet 37:965-972
    • (1985) Am J Hum Genet , vol.37 , pp. 965-972
    • Hassold, T.1    Kumlin, E.2    Takaesu, N.3    Leppert, M.4
  • 12
    • 0026334334 scopus 로고
    • XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
    • Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA (1991) XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet 49:253-260
    • (1991) Am J Hum Genet , vol.49 , pp. 253-260
    • Hassold, T.J.1    Sherman, S.L.2    Pettay, D.3    Page, D.C.4    Jacobs, P.A.5
  • 13
    • 0026800855 scopus 로고
    • Molecular studies of parental origin and mosaicism in 45, X conceptuses
    • Hassold T, Pettay D, Robinson A, Uchida I (1992) Molecular studies of parental origin and mosaicism in 45, X conceptuses. Hum Genet 89:647-652
    • (1992) Hum Genet , vol.89 , pp. 647-652
    • Hassold, T.1    Pettay, D.2    Robinson, A.3    Uchida, I.4
  • 14
    • 0026531326 scopus 로고
    • Mosaicism in Turner Syndrome: Does survival in early pregnancy depend on the presence of two sex chromosomes?
    • Held KR, Kerber S, Kaminsky E, Singh S, Goetz P, Seemanova E, Goedde HW (1992) Mosaicism in Turner Syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes? Hum Genet 88:288-294
    • (1992) Hum Genet , vol.88 , pp. 288-294
    • Held, K.R.1    Kerber, S.2    Kaminsky, E.3    Singh, S.4    Goetz, P.5    Seemanova, E.6    Goedde, H.W.7
  • 15
    • 0020634258 scopus 로고
    • The distribution of chromosomal genotypes associated with Turner's syndrome: Livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural Y abnormalities or mosaicism
    • Hook EB, Warburton D (1983) The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural Y abnormalities or mosaicism. Hum Genet 64:24-27
    • (1983) Hum Genet , vol.64 , pp. 24-27
    • Hook, E.B.1    Warburton, D.2
  • 16
    • 0026752206 scopus 로고
    • The chromosome complement of human gametes
    • Jacobs PA (1992) The chromosome complement of human gametes. Oxf Rev Reprod Biol 14:47-72
    • (1992) Oxf Rev Reprod Biol , vol.14 , pp. 47-72
    • Jacobs, P.A.1
  • 18
    • 0030671186 scopus 로고    scopus 로고
    • Paternal age effect of YY aneuploidy in human sperm, as assessed by fluorescence in situ hybridization
    • Kinakin B, Rademaker A, Martin R (1997) Paternal age effect of YY aneuploidy in human sperm, as assessed by fluorescence in situ hybridization. Cytogenet Cell Genet 78:116-119
    • (1997) Cytogenet Cell Genet , vol.78 , pp. 116-119
    • Kinakin, B.1    Rademaker, A.2    Martin, R.3
  • 19
    • 0028929131 scopus 로고
    • Detection of Y chromosome sequences in a 45,X/46,XXq-patient by southern blot analysis of PCR amplified DNA and fluorescent in situ hybridization (FISH)
    • Kocova M, Siegel SF, Wenger SL, Lee PA, Nalesnik M, Trucco M (1995) Detection of Y chromosome sequences in a 45,X/46,XXq-patient by southern blot analysis of PCR amplified DNA and fluorescent in situ hybridization (FISH). Am J Med Genet 55:483-488
    • (1995) Am J Med Genet , vol.55 , pp. 483-488
    • Kocova, M.1    Siegel, S.F.2    Wenger, S.L.3    Lee, P.A.4    Nalesnik, M.5    Trucco, M.6
  • 20
    • 0028030585 scopus 로고
    • The origin of 47,XXY and 47,XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination
    • MacDonald M, Hassold T, Harvey J, Wang LH, Morton NE, Jacobs P (1994) The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination. Hum Mol Genet 3:1365-1371
    • (1994) Hum Mol Genet , vol.3 , pp. 1365-1371
    • MacDonald, M.1    Hassold, T.2    Harvey, J.3    Wang, L.H.4    Morton, N.E.5    Jacobs, P.6
  • 21
    • 0027462891 scopus 로고
    • A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: Implications for mechanisms of mutation at short tandem repeat loci
    • Mahtani MM, Willard HJ (1993) A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci. Hum Mol Genet 2:431-437
    • (1993) Hum Mol Genet , vol.2 , pp. 431-437
    • Mahtani, M.M.1    Willard, H.J.2
  • 22
    • 0028818839 scopus 로고
    • The relationship between paternal age, sex ratios and aneuploidy frequencies in human sperm, as assessed by multicolor FISH
    • Martin RH, Spriggs E, Ko E, Rademaker A (1995) The relationship between paternal age, sex ratios and aneuploidy frequencies in human sperm, as assessed by multicolor FISH. Am J Hum Genet 57:1395-1399
    • (1995) Am J Hum Genet , vol.57 , pp. 1395-1399
    • Martin, R.H.1    Spriggs, E.2    Ko, E.3    Rademaker, A.4
  • 23
    • 0002684663 scopus 로고
    • Study of aneuploidy frequency of spermatozoa in old and young men, using multi-color fluorescence in situ hybridization (FISH)
    • Miharu N, Best RG, Berete MS, Liu WH, Young SR (1993) Study of aneuploidy frequency of spermatozoa in old and young men, using multi-color fluorescence in situ hybridization (FISH). Am J Hum Genet 53 (Suppl):581
    • (1993) Am J Hum Genet , vol.53 , Issue.SUPPL. , pp. 581
    • Miharu, N.1    Best, R.G.2    Berete, M.S.3    Liu, W.H.4    Young, S.R.5
  • 24
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF (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
  • 26
    • 0025067390 scopus 로고
    • Human insulin receptor gene. Partial sequence and amplification of exons by polymerase chain reaction
    • Seino S, Seino M, Bell GI (1990) Human insulin receptor gene. Partial sequence and amplification of exons by polymerase chain reaction. Diabetes 39:123-128
    • (1990) Diabetes , vol.39 , pp. 123-128
    • Seino, S.1    Seino, M.2    Bell, G.I.3
  • 30
    • 23444437048 scopus 로고
    • Dinucleotide repeat polymorphism at the DXS1283E locus
    • Yen P, Lin H (1994) Dinucleotide repeat polymorphism at the DXS1283E locus. Hum Mol Genet 3:388
    • (1994) Hum Mol Genet , vol.3 , pp. 388
    • Yen, P.1    Lin, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.