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Volumn 30, Issue 9, 2010, Pages 839-844

Is there a correlation between the proportion of cells with isodicentric Yp at amniocentesis and phenotypic sex?

Author keywords

Cytogenetics; FISH; Idic Yp; Normal female; Prenatal diagnosis

Indexed keywords

AMNIOCENTESIS; AMNION CELL; ARTICLE; CHROMOSOMAL INSTABILITY; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME YP; CYTOGENETICS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; HUMAN; PHENOTYPE; PRENATAL SCREENING; PRIORITY JOURNAL; UMBILICAL CORD; UMBILICAL CORD BLOOD;

EID: 77956148948     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2565     Document Type: Article
Times cited : (9)

References (16)
  • 1
    • 33646091762 scopus 로고    scopus 로고
    • Isodicentric Yp: Prenatal diagnosis and outcome in 12 cases
    • Bruyère H, Speevak MD, Winsor EJ, et al. 2006. Isodicentric Yp: prenatal diagnosis and outcome in 12 cases. Prenat Diagn 26: 324-329.
    • (2006) Prenat Diagn , vol.26 , pp. 324-329
    • Bruyère, H.1    Speevak, M.D.2    Winsor, E.J.3
  • 2
    • 0027515332 scopus 로고
    • Yq deletions and AZF locus: Molecular analysis in two fetuses with non familial homogeneous Yq rearrangements
    • Camurri L, Novelli G, Gennarelli M, Cantarelli M, Dallapicolla B. 1993. Yq deletions and AZF locus: molecular analysis in two fetuses with non familial homogeneous Yq rearrangements. Genet Couns 4: 223-226.
    • (1993) Genet Couns , vol.4 , pp. 223-226
    • Camurri, L.1    Novelli, G.2    Gennarelli, M.3    Cantarelli, M.4    Dallapicolla, B.5
  • 3
    • 0001072895 scopus 로고
    • The use of confidence or fiducial limits illustrated in the case of the binomial
    • Clopper C, Pearson ES. 1934. The use of confidence or fiducial limits illustrated in the case of the binomial. Biometrika 26: 404-413.
    • (1934) Biometrika , vol.26 , pp. 404-413
    • Clopper, C.1    Pearson, E.S.2
  • 5
    • 37849021647 scopus 로고    scopus 로고
    • Heterochromatin and RNAi are required to establish CENP-A chromatin at centromeres
    • Folco HD, Pidoux AL, Urano T, Allshire RC. 2008. Heterochromatin and RNAi are required to establish CENP-A chromatin at centromeres. Science. 319(5859): 94-97.
    • (2008) Science , vol.319 , Issue.5859 , pp. 94-97
    • Folco, H.D.1    Pidoux, A.L.2    Urano, T.3    Allshire, R.C.4
  • 7
    • 33748304157 scopus 로고    scopus 로고
    • Determination of the sexual phenotype in a child with 45,X/46,X,Idic(Yp) mosaicism: Importance of the relative proportion of the 45,X line in gonadal tissue
    • Guedes AD, Bianco B, Lipay MV, Brunoni D, de Lourdes Chauffaille M, Verreschi IT. 2006. Determination of the sexual phenotype in a child with 45,X/46,X,Idic(Yp) mosaicism: importance of the relative proportion of the 45,X line in gonadal tissue. Am J Med Genet 140A: 1871-1875.
    • (2006) Am J Med Genet , vol.140 , pp. 1871-1875
    • Guedes, A.D.1    Bianco, B.2    Lipay, M.V.3    Brunoni, D.4    De Lourdes Chauffaille, M.5    Verreschi, I.T.6
  • 8
    • 0036733191 scopus 로고    scopus 로고
    • Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis
    • Hernando C, Carrera M, Ribas I, et al. 2002. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis. Prenat Diagn 22: 802-805.
    • (2002) Prenat Diagn , vol.22 , pp. 802-805
    • Hernando, C.1    Carrera, M.2    Ribas, I.3
  • 9
    • 0028072677 scopus 로고
    • Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases
    • Hsu LY. 1994. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases. Am J Med Genet 53: 108-140.
    • (1994) Am J Med Genet , vol.53 , pp. 108-140
    • Hsu, L.Y.1
  • 10
    • 0036188731 scopus 로고    scopus 로고
    • Prenatal diagnosis of 45,X and 45,X mosaicism: The need for thorough cytogenetic and clinical evaluations
    • Huang B, Thangavelu M, Bhatt SJ Sandlin C, Wang S. 2002. Prenatal diagnosis of 45,X and 45,X mosaicism: the need for thorough cytogenetic and clinical evaluations. Prenat Diagn 22: 105-110.
    • (2002) Prenat Diagn , vol.22 , pp. 105-110
    • Huang, B.1    Thangavelu, M.2    Bhatt, S.J.3    Sandlin, C.4    Wang, S.5
  • 11
    • 50849127858 scopus 로고    scopus 로고
    • Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia
    • Iourov IY, Vorsanova SG, Liehr T, Monakhov VV, Soloviev IV, Yurov YB. 2008. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res 121: 302-306.
    • (2008) Cytogenet Genome Res , vol.121 , pp. 302-306
    • Iourov, I.Y.1    Vorsanova, S.G.2    Liehr, T.3    Monakhov, V.V.4    Soloviev, I.V.5    Yurov, Y.B.6
  • 12
    • 54349096150 scopus 로고    scopus 로고
    • Cytogenetic and molecular analysis of dicentric Y chromosome and its relation to male azoospermia
    • Omrani MD, Hagh JK, Klien W, Gebauer J 2008. Cytogenetic and molecular analysis of dicentric Y chromosome and its relation to male azoospermia. Iran J Reprod Med 6: 57-64.
    • (2008) Iran J Reprod Med , vol.6 , pp. 57-64
    • Omrani, M.D.1    Hagh, J.K.2    Klien, W.3    Gebauer, J.4
  • 13
    • 0025422427 scopus 로고
    • Sex chromosome mosaicism not detected at amniocentesis
    • Roland B, Cox DM, Rudd NL. 1990. Sex chromosome mosaicism not detected at amniocentesis. Prenat Diagn 10: 333-336.
    • (1990) Prenat Diagn , vol.10 , pp. 333-336
    • Roland, B.1    Cox, D.M.2    Rudd, N.L.3
  • 14
    • 0031007675 scopus 로고    scopus 로고
    • Sex chromosome markers: Characterization using fluorescence in situ hybridization and review of the literature
    • Schwartz S, Depinet TW, Leana-Cox J, et al. 1997. Sex chromosome markers: characterization using fluorescence in situ hybridization and review of the literature. Am J Med Genet 71: 1-7.
    • (1997) Am J Med Genet , vol.71 , pp. 1-7
    • Schwartz, S.1    Depinet, T.W.2    Leana-Cox, J.3
  • 15
    • 0028866305 scopus 로고
    • Prenatal identification of i(Yp) by molecular cytogenetic analysis
    • Wang BB, Yu LC, Peng W, Falk RE, Williams J. 1995. Prenatal identification of i(Yp) by molecular cytogenetic analysis. Prenat Diagn 15: 1115-1119.
    • (1995) Prenat Diagn , vol.15 , pp. 1115-1119
    • Wang, B.B.1    Yu, L.C.2    Peng, W.3    Falk, R.E.4    Williams, J.5
  • 16


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.