메뉴 건너뛰기




Volumn 29, Issue 11, 2012, Pages 1299-1304

Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME STRUCTURE; CHROMOSOME TRANSLOCATION 10; CHROMOSOME TRANSLOCATION 15; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC RISK; HUMAN; MALE; MALE INFERTILITY; OLIGOASTHENOTERATOZOOSPERMIA; PREIMPLANTATION GENETIC DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; SEMEN ABNORMALITY; SEMEN ANALYSIS;

EID: 84878367348     PISSN: 10580468     EISSN: 15737330     Source Type: Journal    
DOI: 10.1007/s10815-012-9857-0     Document Type: Article
Times cited : (10)

References (11)
  • 1
  • 2
    • 77952083811 scopus 로고    scopus 로고
    • Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management
    • 20302980 10.1016/j.ejmg.2010.03.003
    • Leclercq S, Auger J, Dupont C, Le Tessier D, Lebbar A, Baverel F, Dupont JM, Eustache F. Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management. Eur J Med Genet. 2010;53(3):127-32.
    • (2010) Eur J Med Genet , vol.53 , Issue.3 , pp. 127-132
    • Leclercq, S.1    Auger, J.2    Dupont, C.3    Le Tessier, D.4    Lebbar, A.5    Baverel, F.6    Dupont, J.M.7    Eustache, F.8
  • 3
    • 0031009264 scopus 로고    scopus 로고
    • Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patents
    • 9187668 10.1007/s004390050443 1:STN:280:DyaK2szjtFegtA%3D%3D
    • Delhanty JDA, Harper JC, Ao A, et al. Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patents. Hum Genet. 1997;99(6):755-60.
    • (1997) Hum Genet , vol.99 , Issue.6 , pp. 755-760
    • Delhanty, J.D.A.1    Harper, J.C.2    Ao, A.3
  • 6
    • 14044257269 scopus 로고    scopus 로고
    • Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques
    • 15567875 10.1093/humrep/deh626 1:STN:280:DC%2BD2M7gtFOjsg%3D%3D
    • Clementini E, Palka C, Iezzi I, Stuppia L, Guanciali-Franchi P, Tiboni GM. Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques. Hum Reprod. 2005;20(2):437-42.
    • (2005) Hum Reprod , vol.20 , Issue.2 , pp. 437-442
    • Clementini, E.1    Palka, C.2    Iezzi, I.3    Stuppia, L.4    Guanciali-Franchi, P.5    Tiboni, G.M.6
  • 7
    • 0031241153 scopus 로고    scopus 로고
    • Mitotic chromosomal anomalies among infertile men
    • 9402306 10.1093/humrep/12.10.2337 1:STN:280:DyaK1c%2Fmtlyqug%3D%3D
    • Bourrouillou G, Calvas P, Bujan L, Mieusset R, Mansat A, Pontonnier F. Mitotic chromosomal anomalies among infertile men. Hum Reprod. 1997;12(10):2337-8.
    • (1997) Hum Reprod , vol.12 , Issue.10 , pp. 2337-2338
    • Bourrouillou, G.1    Calvas, P.2    Bujan, L.3    Mieusset, R.4    Mansat, A.5    Pontonnier, F.6
  • 8
    • 0030455185 scopus 로고    scopus 로고
    • Mitotic chromosomal anomalies among 1210 infertile men
    • 9021359 10.1093/oxfordjournals.humrep.a019178 1:STN:280: DyaK2s7ntlCmsQ%3D%3D
    • Pandiyan N, Jequier AM. Mitotic chromosomal anomalies among 1210 infertile men. Hum Reprod. 1996;11(12):2604-8.
    • (1996) Hum Reprod , vol.11 , Issue.12 , pp. 2604-2608
    • Pandiyan, N.1    Jequier, A.M.2
  • 9
    • 0024469798 scopus 로고
    • Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder
    • 2685311 10.1136/jmg.26.10.626 1:STN:280:DyaK3c%2FmsVCgtw%3D%3D
    • Rivera H, Zuffardi O, Maraschio P, Caiulo A, Anichini C, Scarinci R, Vivarelli R. Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder. J Med Genet. 1989;26(10):626-30.
    • (1989) J Med Genet , vol.26 , Issue.10 , pp. 626-630
    • Rivera, H.1    Zuffardi, O.2    Maraschio, P.3    Caiulo, A.4    Anichini, C.5    Scarinci, R.6    Vivarelli, R.7
  • 10
    • 0033849567 scopus 로고    scopus 로고
    • Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2 - >p15.1: Phenotypic consequences and possible mechanisms
    • 11005146 10.1034/j.1399-0004.2000.580207.x 1:STN:280: DC%2BD3cvltVWlsA%3D%3D
    • Zneimer SM, Cotter PD, Stewart SD. Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2 - >p15.1: phenotypic consequences and possible mechanisms. Clin Genet. 2000;58(2):129-33.
    • (2000) Clin Genet. , vol.58 , Issue.2 , pp. 129-133
    • Zneimer, S.M.1    Cotter, P.D.2    Stewart, S.D.3
  • 11
    • 0035185798 scopus 로고    scopus 로고
    • Pseudo dicentric chromosome (5;21): A rare example of maternal germline mosaicism
    • 11139538 10.1093/humrep/16.1.63 1:STN:280:DC%2BD3M7ktVCitg%3D%3D
    • Engel U, Bohlander SK, Bink K, Hinney B, Laccone F, Bartels I. Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicism. Hum Reprod. 2001;16(1):63-6.
    • (2001) Hum Reprod , vol.16 , Issue.1 , pp. 63-66
    • Engel, U.1    Bohlander, S.K.2    Bink, K.3    Hinney, B.4    Laccone, F.5    Bartels, I.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.