메뉴 건너뛰기




Volumn 12, Issue 5, 1997, Pages 930-937

Chromosomal findings in 150 couples referred for genetic counselling prior to intracytoplasmic sperm injection

Author keywords

Chromosome aberration; Female infertility; Genetic counselling; ICSI; Male infertility

Indexed keywords

ADULT; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME INVERSION; FEMALE; GENETIC COUNSELING; HUMAN; INTRACYTOPLASMIC SPERM INJECTION; MAJOR CLINICAL STUDY; MALE; MARKER CHROMOSOME; RECIPROCAL CHROMOSOME TRANSLOCATION; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SEX CHROMOSOME; SEX CHROMOSOME MOSAICISM;

EID: 1842411314     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/12.5.930     Document Type: Article
Times cited : (88)

References (49)
  • 1
    • 0029921074 scopus 로고    scopus 로고
    • Results of cytogenetic analysis in men with severe subfertility prior to intracytoplasmic sperm injection
    • Baschat, A.A.K., Küpker, W., Al Hasani, S. et al. (1996) Results of cytogenetic analysis in men with severe subfertility prior to intracytoplasmic sperm injection. Hum. Reprod., 11, 330-333.
    • (1996) Hum. Reprod. , vol.11 , pp. 330-333
    • Baschat, A.A.K.1    Küpker, W.2    Al Hasani, S.3
  • 2
    • 0023186887 scopus 로고
    • Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42)
    • Batanian, J. and Hulten, M.A. (1987) Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Hum. Genet., 76, 81-89.
    • (1987) Hum. Genet. , vol.76 , pp. 81-89
    • Batanian, J.1    Hulten, M.A.2
  • 3
    • 0022349299 scopus 로고
    • Chromosome studies in 952 infertile males with a sperm count below 10 million/ml
    • Bourrouillou, G., Dastugue, N. and Colombies, P. (1985) Chromosome studies in 952 infertile males with a sperm count below 10 million/ml. Hum. Genet., 71, 366-367.
    • (1985) Hum. Genet. , vol.71 , pp. 366-367
    • Bourrouillou, G.1    Dastugue, N.2    Colombies, P.3
  • 4
    • 0023557454 scopus 로고
    • Chromosome anomalies and male infertility. A study of 1444 subjects
    • Bourrouillou, G., Mansat, A., Calvas, P. et al. (1987) Chromosome anomalies and male infertility. A study of 1444 subjects. Bull. Assoc. Anat. Nancy, 71, 29-31.
    • (1987) Bull. Assoc. Anat. Nancy , vol.71 , pp. 29-31
    • Bourrouillou, G.1    Mansat, A.2    Calvas, P.3
  • 5
    • 0026849633 scopus 로고
    • Role and contribution of karyotyping in male infertility
    • Bourrouillou, G., Bujan, L., Calvas, P. et al. (1992) Role and contribution of karyotyping in male infertility. Prog. Urol., 2, 189-195.
    • (1992) Prog. Urol. , vol.2 , pp. 189-195
    • Bourrouillou, G.1    Bujan, L.2    Calvas, P.3
  • 6
    • 0022504805 scopus 로고
    • Cytogenetics of human sperm: Meiotic segregation in two translocation carriers
    • Brandriff, B., Gordon, L., Ashworth, L.K. et al. (1986) Cytogenetics of human sperm: meiotic segregation in two translocation carriers. Am. J. Hum. Genet., 38, 197-208.
    • (1986) Am. J. Hum. Genet. , vol.38 , pp. 197-208
    • Brandriff, B.1    Gordon, L.2    Ashworth, L.K.3
  • 7
    • 0029004732 scopus 로고
    • A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12 699 prenatal samples
    • Brondum-Nielsen, K. and Mikkelsen, M. (1995) A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12 699 prenatal samples. Prenat. Diagn., 15, 615-619.
    • (1995) Prenat. Diagn. , vol.15 , pp. 615-619
    • Brondum-Nielsen, K.1    Mikkelsen, M.2
  • 8
    • 0026680297 scopus 로고
    • Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes
    • Callen, D.F., Eyre, H., Yip, M.Y. et al. (1992) Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes. Am. J. Med. Genet., 43, 709-715.
    • (1992) Am. J. Med. Genet. , vol.43 , pp. 709-715
    • Callen, D.F.1    Eyre, H.2    Yip, M.Y.3
  • 9
    • 0019970869 scopus 로고
    • The effect of variant chromosomes on reproductive fitness in man
    • Carothers, A.D., Buckton, K.E., Collyer, S. et al. (1982) The effect of variant chromosomes on reproductive fitness in man. Clin. Genet., 21, 280-289.
    • (1982) Clin. Genet. , vol.21 , pp. 280-289
    • Carothers, A.D.1    Buckton, K.E.2    Collyer, S.3
  • 10
    • 0029025333 scopus 로고
    • Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
    • Chillon, M., Casals, T., Mercier, B. et al. (1995) Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N. Engl. J. Med., 332, 1475-1480.
    • (1995) N. Engl. J. Med. , vol.332 , pp. 1475-1480
    • Chillon, M.1    Casals, T.2    Mercier, B.3
  • 11
    • 0028033069 scopus 로고
    • Population variation of common cystic fibrosis mutations
    • Cystic Fibrosis Genetic Analysis Consortium (1994) Population variation of common cystic fibrosis mutations. Hum, Mutat., 4, 167-177.
    • (1994) Hum, Mutat. , vol.4 , pp. 167-177
  • 12
    • 0024412088 scopus 로고
    • Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories
    • Daniel, A., Hook, E.B. and Wulf, G. (1989) Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. Am. J. Med. Genet., 31, 14-53.
    • (1989) Am. J. Med. Genet. , vol.31 , pp. 14-53
    • Daniel, A.1    Hook, E.B.2    Wulf, G.3
  • 13
    • 0025922098 scopus 로고
    • Cytogenetic studies in male infertility: A review
    • De Braekeleer, M. and Dao, T.-N. (1991) Cytogenetic studies in male infertility: a review. Hum. Reprod., 6, 245-250.
    • (1991) Hum. Reprod. , vol.6 , pp. 245-250
    • De Braekeleer, M.1    Dao, T.-N.2
  • 15
    • 0030032379 scopus 로고    scopus 로고
    • Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): Correlation between genotype and phenotype
    • Dumur, V., Gervais, R., Rigot, J.M. et al. (1996) Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype. Hum. Genet., 97, 7-10.
    • (1996) Hum. Genet. , vol.97 , pp. 7-10
    • Dumur, V.1    Gervais, R.2    Rigot, J.M.3
  • 16
    • 0023444068 scopus 로고
    • High incidence of minor chromosomal variants in teratozoospermic males
    • Eiben, B., Leipoldt, M., Rammeisberg, O. et al. (1987) High incidence of minor chromosomal variants in teratozoospermic males. Andrologia, 19, 684-687.
    • (1987) Andrologia , vol.19 , pp. 684-687
    • Eiben, B.1    Leipoldt, M.2    Rammeisberg, O.3
  • 17
    • 0029928789 scopus 로고    scopus 로고
    • Complexity in a monogenetic disease
    • Estivill, X. (1996) Complexity in a monogenetic disease. Nature Genet., 12, 348-350.
    • (1996) Nature Genet. , vol.12 , pp. 348-350
    • Estivill, X.1
  • 20
    • 0025633209 scopus 로고
    • Infertility in human males with autosomal translocations: Meiotic study of a 14;22 Robertsonian translocation
    • Guichaoua, M.R., Quack, B., Speed, R.M. et al. (1990) Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation. Hum. Genet., 86, 162-166.
    • (1990) Hum. Genet. , vol.86 , pp. 162-166
    • Guichaoua, M.R.1    Quack, B.2    Speed, R.M.3
  • 21
    • 0026683520 scopus 로고
    • Infertility in human males with autosomal translocations
    • Guichaoua, M.R., Speed, R.M., Luciani, J.M. et al. (1992) Infertility in human males with autosomal translocations. Cytogenet. Cell. Genet., 60, 96-101.
    • (1992) Cytogenet. Cell. Genet. , vol.60 , pp. 96-101
    • Guichaoua, M.R.1    Speed, R.M.2    Luciani, J.M.3
  • 23
    • 0028264560 scopus 로고
    • Female infertility: Causes and treatment
    • Healy, D.L., Tounson, A.O. and Andersen, A.N. (1994) Female infertility: causes and treatment. Lancet, 343, 1539-1544.
    • (1994) Lancet , vol.343 , pp. 1539-1544
    • Healy, D.L.1    Tounson, A.O.2    Andersen, A.N.3
  • 24
    • 0023878669 scopus 로고
    • Chromosome aberrations in 500 couples referred for in-vitro fertilization or related fertility treatment
    • Hens, L., Bonduelle, M., Liebaers, I. et al. (1988) Chromosome aberrations in 500 couples referred for in-vitro fertilization or related fertility treatment. Hum. Reprod., 3, 451-457.
    • (1988) Hum. Reprod. , vol.3 , pp. 451-457
    • Hens, L.1    Bonduelle, M.2    Liebaers, I.3
  • 25
    • 0028072677 scopus 로고
    • Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis in structural aberrations in postnatal diagnosed cases
    • Hsu, L.Y.F. (1994) Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis in structural aberrations in postnatal diagnosed cases. Am. J. Med. Genet., 53, 108-140.
    • (1994) Am. J. Med. Genet. , vol.53 , pp. 108-140
    • Hsu, L.Y.F.1
  • 26
    • 0027287267 scopus 로고
    • The effect of 13;14 Robertsonian translocations on germ-cell differentiation in infertile males
    • Johannisson, R., Schwinger, E., Wolff, H.H. et al. (1993) The effect of 13;14 Robertsonian translocations on germ-cell differentiation in infertile males. Cytogenet. Cell Genet., 63, 151-155.
    • (1993) Cytogenet. Cell Genet. , vol.63 , pp. 151-155
    • Johannisson, R.1    Schwinger, E.2    Wolff, H.H.3
  • 28
    • 0024445505 scopus 로고
    • Cytogenetic survey of subfertile males in Japan
    • Matsuda, T., Nonomura, M., Okada, K. et al. (1989) Cytogenetic survey of subfertile males in Japan. Urol. Int., 44, 194-197.
    • (1989) Urol. Int. , vol.44 , pp. 194-197
    • Matsuda, T.1    Nonomura, M.2    Okada, K.3
  • 29
    • 0026340954 scopus 로고
    • Quantitative analysis of seminiferous epithelium in subfertile carriers of chromosomal translocations
    • Matsuda, T., Horii, Y., Hayashi, K. et al. (1991) Quantitative analysis of seminiferous epithelium in subfertile carriers of chromosomal translocations. Int. J. Fenil., 36, 344-351.
    • (1991) Int. J. Fenil. , vol.36 , pp. 344-351
    • Matsuda, T.1    Horii, Y.2    Hayashi, K.3
  • 30
    • 0021365627 scopus 로고
    • Chromosomal constitution of infertile men
    • Micic, M., Micic, S. and Diklic, V. (1984) Chromosomal constitution of infertile men. Clin. Genet., 25, 33-36.
    • (1984) Clin. Genet. , vol.25 , pp. 33-36
    • Micic, M.1    Micic, S.2    Diklic, V.3
  • 31
    • 0026552763 scopus 로고
    • Experiences with risk estimates for carriers of chromosomal reciprocal translocations
    • Midro, A.T., Stengel-Rutkowski, S. and Stene, J. (1992) Experiences with risk estimates for carriers of chromosomal reciprocal translocations. Clin. Genet., 41, 113-122.
    • (1992) Clin. Genet. , vol.41 , pp. 113-122
    • Midro, A.T.1    Stengel-Rutkowski, S.2    Stene, J.3
  • 32
    • 0023192398 scopus 로고
    • A new case of (Y;1) balanced translocation in an infertile man with Hodgkin's disease
    • Moreau, N., Teyssier, M., Rollet, J. et al. (1987) A new case of (Y;1) balanced translocation in an infertile man with Hodgkin's disease. J. Med. Genet., 24, 379-380.
    • (1987) J. Med. Genet. , vol.24 , pp. 379-380
    • Moreau, N.1    Teyssier, M.2    Rollet, J.3
  • 33
    • 0018778138 scopus 로고
    • Genetic causes and workup of male and female infertility. 2. Abnormality presenting between birth and adult life
    • Opitz, J.M., Shapiro, S.S. and Uehling, D.T. (1979) Genetic causes and workup of male and female infertility. 2. Abnormality presenting between birth and adult life. Postgrad. Med. J., 65, 157-162, 164, 166.
    • (1979) Postgrad. Med. J. , vol.65 , pp. 157-162
    • Opitz, J.M.1    Shapiro, S.S.2    Uehling, D.T.3
  • 34
    • 0025363466 scopus 로고
    • Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature
    • Pellestor, F. (1990) Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature. Hum. Genet., 85, 49-54.
    • (1990) Hum. Genet. , vol.85 , pp. 49-54
    • Pellestor, F.1
  • 35
    • 0029973468 scopus 로고    scopus 로고
    • Debate. Genetic consequences of ICSI. Is ICSI associated with risks of genetic disease? Implications for counselling, practice and research
    • Persson, J.W., Peters, G.B. and Saunders, D.M. (1996) Debate. Genetic consequences of ICSI. Is ICSI associated with risks of genetic disease? Implications for counselling, practice and research. Hum. Reprod., 11, 921-932.
    • (1996) Hum. Reprod. , vol.11 , pp. 921-932
    • Persson, J.W.1    Peters, G.B.2    Saunders, D.M.3
  • 36
    • 0028961695 scopus 로고
    • Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases
    • Pettenati, M.J., Rao, P.N., Phelan, M.C. et al. (1995) Paracentric inversions in humans: a review of 446 paracentric inversions with presentation of 120 new cases. Am. J. Med. Genet., 55, 171-187.
    • (1995) Am. J. Med. Genet. , vol.55 , pp. 171-187
    • Pettenati, M.J.1    Rao, P.N.2    Phelan, M.C.3
  • 37
    • 0026680691 scopus 로고
    • Uniparental disomy 15 resulting from 'correction' of an initial trisomy 15
    • Purvis-Smith, S.G., Saville, T., Manass, S. et al. (1992) Uniparental disomy 15 resulting from 'correction' of an initial trisomy 15. Am. J. Hum. Genet., 50, 1348-1350.
    • (1992) Am. J. Hum. Genet. , vol.50 , pp. 1348-1350
    • Purvis-Smith, S.G.1    Saville, T.2    Manass, S.3
  • 38
    • 0023201791 scopus 로고
    • Cytogenetic evaluation of 163 azoospermics
    • Rivas, F., Garcia-Esqoivel, L., Diaz, M. et al. (1987) Cytogenetic evaluation of 163 azoospermics. J. Génét. Hum., 35, 291-298.
    • (1987) J. Génét. Hum. , vol.35 , pp. 291-298
    • Rivas, F.1    Garcia-Esqoivel, L.2    Diaz, M.3
  • 39
    • 0029923718 scopus 로고    scopus 로고
    • Sperm chromatin anomalies can influence decondensation after intracytoplasmic sperm injection
    • Sakkas, D., Urner, F., Bianchi, P.G. et al. (1996) Sperm chromatin anomalies can influence decondensation after intracytoplasmic sperm injection. Hum. Reprod., 11, 837-843.
    • (1996) Hum. Reprod. , vol.11 , pp. 837-843
    • Sakkas, D.1    Urner, F.2    Bianchi, P.G.3
  • 40
    • 0027196455 scopus 로고
    • Y-Autosorne translocation associated with azoospermia
    • Sasagawa, I., Nakada, T., Adachi, Y. et al. (1993) Y-Autosorne translocation associated with azoospermia. Scand. J. Urol. Nephrol., 27, 285-288.
    • (1993) Scand. J. Urol. Nephrol. , vol.27 , pp. 285-288
    • Sasagawa, I.1    Nakada, T.2    Adachi, Y.3
  • 41
    • 0027184854 scopus 로고
    • Genomic imprinting: Consequences of uniparental disomy for human disease
    • Schinzel, A. (1993) Genomic imprinting: consequences of uniparental disomy for human disease. Am. J. Med. Genet., 46, 683-684.
    • (1993) Am. J. Med. Genet. , vol.46 , pp. 683-684
    • Schinzel, A.1
  • 42
    • 0025833695 scopus 로고
    • Pericentric inversion of chromosome 5: A possible threat to male fertility?
    • Simi, P., Voliani, S., Rossi, S. et al. (1991) Pericentric inversion of chromosome 5: a possible threat to male fertility? Acta Eur. Fertil., 22, 117-119.
    • (1991) Acta Eur. Fertil. , vol.22 , pp. 117-119
    • Simi, P.1    Voliani, S.2    Rossi, S.3
  • 43
    • 0028283038 scopus 로고
    • Pathogenesis and management of male infertility
    • Skakkebaek, N.E., Giwercman, A. and De Kretser, D. (1994) Pathogenesis and management of male infertility. Lancet, 343, 1473-1479.
    • (1994) Lancet , vol.343 , pp. 1473-1479
    • Skakkebaek, N.E.1    Giwercman, A.2    De Kretser, D.3
  • 44
    • 0021015403 scopus 로고
    • The genetic significance of accessory bisatellited marker chromosomes
    • Steinbach, P., Djalali, M., Hansmann, I. et al. (1983) The genetic significance of accessory bisatellited marker chromosomes. Hum. Genet., 65, 155-164.
    • (1983) Hum. Genet. , vol.65 , pp. 155-164
    • Steinbach, P.1    Djalali, M.2    Hansmann, I.3
  • 46
    • 0027997871 scopus 로고
    • Detection of low level sex-chromosomal mosaicism
    • Toncheva, D., Ilieva, P. and Mavrudieva, M. (1994) Detection of low level sex-chromosomal mosaicism. Genet. Couns., 5, 363-367.
    • (1994) Genet. Couns. , vol.5 , pp. 363-367
    • Toncheva, D.1    Ilieva, P.2    Mavrudieva, M.3
  • 47
    • 0022633253 scopus 로고
    • Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents
    • Uchida, I.A. and Freeman, V.C.P. (1986) Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents. Hum. Genet., 72, 118-122.
    • (1986) Hum. Genet. , vol.72 , pp. 118-122
    • Uchida, I.A.1    Freeman, V.C.P.2
  • 49
    • 0029616734 scopus 로고
    • Cystic fibrosis: Genotypic and phenotypic variations
    • Zielinski, J. and Tsui, L.-C. (1995) Cystic fibrosis: genotypic and phenotypic variations. Annu. Rev. Genet., 29, 777-807.
    • (1995) Annu. Rev. Genet. , vol.29 , pp. 777-807
    • Zielinski, J.1    Tsui, L.-C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.