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Volumn 10, Issue 5, 2002, Pages 303-312

Guidelines for the appropriate use of genetic tests in infertile couples

Author keywords

Female infertility; Genetics; Male infertility; Mutations

Indexed keywords

ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; FEMALE; FEMALE INFERTILITY; FERTILIZATION IN VITRO; GENETIC ANALYSIS; GOOD CLINICAL PRACTICE; HUMAN; ITALY; MALE; MALE INFERTILITY; MEDICAL DECISION MAKING; MEDICAL EXPERT; MEDICAL RESEARCH; MEDICAL SOCIETY; PRACTICE GUIDELINE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROGNOSIS; REPRODUCTION; RISK ASSESSMENT;

EID: 0036063359     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200805     Document Type: Article
Times cited : (137)

References (82)
  • 8
    • 0343986287 scopus 로고    scopus 로고
    • Optimal use of infertility diagnostic tests and treatments
    • The ESHRE Capri Workshop Group
    • (2000) Hum. Reprod , vol.15 , pp. 723-732
  • 9
    • 84997060692 scopus 로고    scopus 로고
    • WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction
    • World Health Organization Cambridge: Cambridge University Press
    • (1999)
  • 17
    • 0035187717 scopus 로고    scopus 로고
    • Chromosomal factors on infertility in candidate couples for ICSI: An equal risk of constitutional aberrations in women and men
    • (2001) Hum. Reprod , vol.16 , pp. 82-90
    • Gekas, J.1    Thepot, F.2    Turleau, C.3
  • 18
    • 0031943492 scopus 로고    scopus 로고
    • Chromosome abnormalities in 447 couples undergoing intracytoplasmic sperm injection - Prevalence, types, sex distribution and reproductive relevance
    • (1998) Hum. Reprod , vol.13 , pp. 576-582
    • Meschede, D.1    Lemcke, B.2    Exeler, J.R.3
  • 31
    • 0017119580 scopus 로고
    • Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
    • (1976) Hum. Genet , vol.34 , pp. 119-124
    • Tiepolo, L.1    Zuffardi, O.2
  • 34
    • 0005701785 scopus 로고
    • Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
    • (1995) Nat. Genet , vol.14 , pp. 292-299
    • Reijo, R.1    Lee, T.Y.2    Salo, P.3
  • 45
    • 0033803792 scopus 로고    scopus 로고
    • Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens
    • (2000) Hum. Reprod , vol.15 , pp. 1476-1483
    • Casals, T.1    Bassas, L.2    Egozcue, S.3
  • 46
    • 0029086620 scopus 로고
    • Congenital unilateral absence of the vas deferens: A heterogeneous disorder with two distinct supopulations based upon aetiology and mutational status of the cystic fibrosis gene
    • (1995) Hum. Reprod , vol.10 , pp. 1728-1735
    • Mickle, J.1    Milunsky, A.2    Amos, J.A.3    Oates, R.D.4
  • 48
    • 0029077209 scopus 로고
    • The use of epididymal and testicular spermatozoa for intracytoplasmic sperm injection: The genetic implications for male infertility
    • (1995) Hum. Reprod , vol.10 , pp. 2031-2043
    • Silber, S.J.1    Nagy, Z.2    Liu, J.3
  • 74
    • 0033911231 scopus 로고    scopus 로고
    • Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect?
    • (2000) Am. J. Hum. Genet , vol.67 , pp. 11-13
    • Sherman, S.L.1
  • 82
    • 0031698004 scopus 로고    scopus 로고
    • Genetic risks of intracytoplasmic sperm injection in the treatment of male infertilità: Recommendations for genetic counselling and screening
    • (1998) Fertil. Steril , vol.70 , pp. 397-411
    • Johnson, M.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.