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Volumn 179, Issue 4, 2008, Pages 1499-1505

The Relative Accuracy of a Questionnaire Compared With Pedigree Analysis in Genetic Risk Assessment for Infertility

Author keywords

genetic counseling; genetics; infertility; male; reproductive medicine

Indexed keywords

ACCURACY; ADULT; ARTICLE; BIRTH DEFECT; COMPARATIVE STUDY; CONGENITAL HEART MALFORMATION; DEVELOPMENTAL DISORDER; FAMILY HISTORY; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC RISK; GOLD STANDARD; HUMAN; INTERMETHOD COMPARISON; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; MENTAL DEFICIENCY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; QUESTIONNAIRE; RISK ASSESSMENT; SENSITIVITY AND SPECIFICITY; SPONTANEOUS ABORTION; STILLBIRTH;

EID: 40849083277     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.juro.2007.11.056     Document Type: Article
Times cited : (3)

References (20)
  • 1
    • 0042123550 scopus 로고    scopus 로고
    • Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions
    • Hopps C.V., Mielnik A., Goldstein M., Palermo G.D., Rosenwaks Z., and Schlegel P.N. Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions. Hum Reprod 18 (2003) 1660
    • (2003) Hum Reprod , vol.18 , pp. 1660
    • Hopps, C.V.1    Mielnik, A.2    Goldstein, M.3    Palermo, G.D.4    Rosenwaks, Z.5    Schlegel, P.N.6
  • 2
    • 0036865853 scopus 로고    scopus 로고
    • Current and future genetic screening for male infertility
    • Turek P.J., and Reijo Pera R.A. Current and future genetic screening for male infertility. Urol Clin North Am 29 (2002) 767
    • (2002) Urol Clin North Am , vol.29 , pp. 767
    • Turek, P.J.1    Reijo Pera, R.A.2
  • 3
    • 0026562867 scopus 로고
    • Congenital bilateral absence of the vas deferens: a primarily genital form of cystic fibrosis
    • Anguiano A., Oates R.D., Amos J.A., Dean M., Gerrard B., Stewart C., et al. Congenital bilateral absence of the vas deferens: a primarily genital form of cystic fibrosis. JAMA 267 (1992) 1794
    • (1992) JAMA , vol.267 , pp. 1794
    • Anguiano, A.1    Oates, R.D.2    Amos, J.A.3    Dean, M.4    Gerrard, B.5    Stewart, C.6
  • 4
    • 0028791190 scopus 로고
    • Frequent occurrences of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absences of the vas deferens
    • Costes B., Girodon E., Ghanem N., Flori E., Jardin A., Soufir J.C., et al. Frequent occurrences of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absences of the vas deferens. Eur J Hum Genet 3 (1995) 285
    • (1995) Eur J Hum Genet , vol.3 , pp. 285
    • Costes, B.1    Girodon, E.2    Ghanem, N.3    Flori, E.4    Jardin, A.5    Soufir, J.C.6
  • 5
    • 0029025333 scopus 로고
    • Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
    • Chillon M., Casals T., Mercier B., Bassas L., Lissens W., Silber S., et al. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N Engl J Med 332 (1995) 1475
    • (1995) N Engl J Med , vol.332 , pp. 1475
    • Chillon, M.1    Casals, T.2    Mercier, B.3    Bassas, L.4    Lissens, W.5    Silber, S.6
  • 6
    • 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., Gervias R., Rigot J.M., Delomel-Vinner E., Decaestecker B., Lafitte J.J., et al. Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype. Hum Genet 97 (1996) 7
    • (1996) Hum Genet , vol.97 , pp. 7
    • Dumur, V.1    Gervias, R.2    Rigot, J.M.3    Delomel-Vinner, E.4    Decaestecker, B.5    Lafitte, J.J.6
  • 7
    • 40849103184 scopus 로고    scopus 로고
    • Novel missense mutations of the Deleted-in-AZoospermia-Like (DAZL) gene in infertile women and men
    • Tung J., Rosen M.P., Nelson L.M., Turek P.J., Witte J.S., Cramer D.W., et al. Novel missense mutations of the Deleted-in-AZoospermia-Like (DAZL) gene in infertile women and men. Reprod Biol Endocrinol 2 (2001) 40
    • (2001) Reprod Biol Endocrinol , vol.2 , pp. 40
    • Tung, J.1    Rosen, M.P.2    Nelson, L.M.3    Turek, P.J.4    Witte, J.S.5    Cramer, D.W.6
  • 8
    • 0030811796 scopus 로고    scopus 로고
    • Family history: a comprehensive genetic risk assessment for the chronic conditions of adulthood
    • Scheuner M.T., Wang S.J., Raffel L.J., Larabell S.K., and Rotter J.I. Family history: a comprehensive genetic risk assessment for the chronic conditions of adulthood. Am J Med Genet 71 (1997) 315
    • (1997) Am J Med Genet , vol.71 , pp. 315
    • Scheuner, M.T.1    Wang, S.J.2    Raffel, L.J.3    Larabell, S.K.4    Rotter, J.I.5
  • 9
    • 0033037429 scopus 로고    scopus 로고
    • Family history taking and genetic counselling in primary care
    • Rose P., Humm E., Hey K., Jones L., and Huson S.M. Family history taking and genetic counselling in primary care. Fam Pract 16 (1999) 78
    • (1999) Fam Pract , vol.16 , pp. 78
    • Rose, P.1    Humm, E.2    Hey, K.3    Jones, L.4    Huson, S.M.5
  • 10
    • 0033646497 scopus 로고    scopus 로고
    • The practical importance of pedigree analysis in women considering invasive prenatal diagnosis for advanced maternal age or abnormal serum screening tests
    • Meschede D., Albersmann S., and Horst J. The practical importance of pedigree analysis in women considering invasive prenatal diagnosis for advanced maternal age or abnormal serum screening tests. Prenat Diagn 20 (2000) 865
    • (2000) Prenat Diagn , vol.20 , pp. 865
    • Meschede, D.1    Albersmann, S.2    Horst, J.3
  • 11
    • 4444255884 scopus 로고    scopus 로고
    • Information on commonly asked questions about genetic evaluation and counseling for infertile couples
    • Practice Committee of the American Society for Reproductive Medicine
    • Practice Committee of the American Society for Reproductive Medicine. Information on commonly asked questions about genetic evaluation and counseling for infertile couples. Fertil Steril 82 (2004) S97
    • (2004) Fertil Steril , vol.82
  • 12
    • 0346725834 scopus 로고    scopus 로고
    • The art of taking a history
    • Tulandi T., and Platt R. The art of taking a history. Fertil Steril 81 (2004) 11
    • (2004) Fertil Steril , vol.81 , pp. 11
    • Tulandi, T.1    Platt, R.2
  • 13
    • 40849086941 scopus 로고
    • Antenatal Diagnosis of Genetic Disorders
    • American College of Obstetricians and Gynecologists Washington, D. C.
    • American College of Obstetricians and Gynecologists. Antenatal Diagnosis of Genetic Disorders. ACOG Technical Bulletin No. 188 (1987) Washington, D. C.
    • (1987) ACOG Technical Bulletin No. 188
  • 14
    • 40849113827 scopus 로고    scopus 로고
    • United States Department of Health and Human Services Accessed April 20, 2006
    • United States Department of Health and Human Services. US Surgeon General's Family Health History Initiative. http://www.hhs.gov/familyhistory/ Accessed April 20, 2006
    • US Surgeon General's Family Health History Initiative
  • 18
    • 0032195409 scopus 로고    scopus 로고
    • Primary care physician's utilization and perceptions of genetic services
    • Hayflick S.J., Eiff M.P., Carpenter L., and Steinberger J. Primary care physician's utilization and perceptions of genetic services. Genet Med 1 (1998) 13
    • (1998) Genet Med , vol.1 , pp. 13
    • Hayflick, S.J.1    Eiff, M.P.2    Carpenter, L.3    Steinberger, J.4
  • 19
    • 0034532295 scopus 로고    scopus 로고
    • Family history-taking in community family practice: implications for genetic screening
    • Acheson L.S., Wiesner G.L., Zyzanski S.J., Goodwin M.A., and Stange K.C. Family history-taking in community family practice: implications for genetic screening. Genet Med 2 (2000) 180
    • (2000) Genet Med , vol.2 , pp. 180
    • Acheson, L.S.1    Wiesner, G.L.2    Zyzanski, S.J.3    Goodwin, M.A.4    Stange, K.C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.