메뉴 건너뛰기




Volumn 26, Issue 2, 2006, Pages 134-137

Natural history of prenatally diagnosed 46,X,isodicentric Y

Author keywords

Isodicentric Y chromosome; Natural history; Prenatal diagnosis

Indexed keywords

ARTICLE; CARDIOVASCULAR DISEASE; CHILD; CHROMOSOME ABERRATION; CLINICAL ARTICLE; DICENTRIC CHROMOSOME; FEMALE; FEMALE GENITAL SYSTEM; HISTORY; HUMAN; INFANT; KARYOTYPE 45,X; KARYOTYPE 46,XX; KARYOTYPING; MALE; MALE GENITAL SYSTEM; MEDICAL LITERATURE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TURNER SYNDROME;

EID: 33344458754     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1352     Document Type: Article
Times cited : (23)

References (16)
  • 1
    • 0030948448 scopus 로고    scopus 로고
    • 47,XXY (Klinefelter syndrome) and 47,XYY: Estimated rates of and indication for postnatal diagnosis with implications for prenatal counseling
    • Abramsky L, Chapple J. 1997. 47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counseling. Prenat Diagn 17-4: 363-368.
    • (1997) Prenat Diagn , vol.17 , Issue.4 , pp. 363-368
    • Abramsky, L.1    Chapple, J.2
  • 2
    • 0026731350 scopus 로고
    • Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y-chromosome marker, idic(Yp)
    • Bernstein R, Steinhaus KA, Cain MJ. 1992. Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y-chromosome marker, idic(Yp). Prenat Diagn 12: 709-716.
    • (1992) Prenat Diagn , vol.12 , pp. 709-716
    • Bernstein, R.1    Steinhaus, K.A.2    Cain, M.J.3
  • 3
    • 0027515332 scopus 로고
    • Yq deletions and AZF locus: Molecular analysis in two fetuses with nonfamilial 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 nonfamilial 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
  • 4
    • 0025177372 scopus 로고
    • The phenotype of 45,X/46,XY mosaicism: An analysis of 92 prenatally diagnosed cases
    • Chang HJ, Clark RD, Bachman H. 1990. The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases. Am J Hum Genet 46: 156-167.
    • (1990) Am J Hum Genet , vol.46 , pp. 156-167
    • Chang, H.J.1    Clark, R.D.2    Bachman, H.3
  • 5
    • 12744260259 scopus 로고    scopus 로고
    • The endless quest for sex determination genes
    • Fleming A, Vilain E. 2005. The endless quest for sex determination genes. Clin Genet 67(1): 15-25.
    • (2005) Clin Genet , vol.67 , Issue.1 , pp. 15-25
    • Fleming, A.1    Vilain, E.2
  • 6
    • 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
  • 7
    • 0024508414 scopus 로고
    • Prenatal diagnosis of 45,X/46,XY mosaicism. A review and uptake
    • Hsu LYF. 1989. Prenatal diagnosis of 45,X/46,XY mosaicism. A review and uptake. Prenat Diagn 9: 31-48.
    • (1989) Prenat Diagn , vol.9 , pp. 31-48
    • Hsu, L.Y.F.1
  • 8
    • 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 S, Sanlin CJ, 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.3    Sanlin, C.J.4    Wang, S.5
  • 9
    • 0028788961 scopus 로고
    • Increased incidence of cytogenetic abnormalities in chorionic villus samples from pregnancies established by in vitro fertilization and embryo transfer (IVF-ET)
    • In't Veld PA, Van Opstal D, Van Den Berg C, et al. 1995. Increased incidence of cytogenetic abnormalities in chorionic villus samples from pregnancies established by in vitro fertilization and embryo transfer (IVF-ET). Prenat Diagn 15: 975-980.
    • (1995) Prenat Diagn , vol.15 , pp. 975-980
    • In't Veld, P.A.1    Van Opstal, D.2    Van Den Berg, C.3
  • 10
    • 0036908813 scopus 로고    scopus 로고
    • SHOX haploinsufficiency and its modifying factors
    • Ogata T. 2002. SHOX haploinsufficiency and its modifying factors. J Pediatr Endocrinol Metab 15(Suppl. 5): 1289-1294.
    • (2002) J Pediatr Endocrinol Metab , vol.15 , Issue.SUPPL. 5 , pp. 1289-1294
    • Ogata, T.1
  • 11
    • 0018361397 scopus 로고
    • Sixteen years' experience of counseling, diagnosis, and prenatal detection in one Genetic Centre: Progress, results, and problems
    • Polani PE, Alberman E, Alexander BJ, et al. 1979. Sixteen years' experience of counseling, diagnosis, and prenatal detection in one Genetic Centre: progress, results, and problems. J Med Genet 16: 166-175.
    • (1979) J Med Genet , vol.16 , pp. 166-175
    • Polani, P.E.1    Alberman, E.2    Alexander, B.J.3
  • 12
    • 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
  • 13
    • 0342502138 scopus 로고    scopus 로고
    • Cytogenetic and molecular characterization of two isodicentric Y chromosomes
    • Stankiewicz P, Helias-Rodzewicz Z, Jakubow-Durska K, et al. 2001. Cytogenetic and molecular characterization of two isodicentric Y chromosomes. Am J Med Genet 101: 20-25.
    • (2001) Am J Med Genet , vol.101 , pp. 20-25
    • Stankiewicz, P.1    Helias-Rodzewicz, Z.2    Jakubow-Durska, K.3
  • 14
    • 0028997526 scopus 로고
    • Isodicentric Y chromosome: Cytogenetic, molecular and clinical studies and review of the literature
    • Tuck-Muller CM, Chen H, Martinez JE, et al. 1995. Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. Hum Genet 96: 119-129.
    • (1995) Hum Genet , vol.96 , pp. 119-129
    • Tuck-Muller, C.M.1    Chen, H.2    Martinez, J.E.3
  • 15
    • 20444480612 scopus 로고    scopus 로고
    • New insights into the regulation of mammalian sex determination and male sex differentiation
    • Viger RS, Silversides DW, Tremblay JJ. 2005. New insights into the regulation of mammalian sex determination and male sex differentiation. Vitam Horm 70: 387-413.
    • (2005) Vitam Horm , vol.70 , pp. 387-413
    • Viger, R.S.1    Silversides, D.W.2    Tremblay, J.J.3
  • 16
    • 0023905065 scopus 로고
    • 45,X/46,XY mosaicism: Contrast of prenatal and postnatal diagnosis
    • Wheeler M, Peakman D, Robinson S, Henry G. 1988. 45,X/46,XY mosaicism: contrast of prenatal and postnatal diagnosis. Am J Med Genet 29: 565-571.
    • (1988) Am J Med Genet , vol.29 , pp. 565-571
    • Wheeler, M.1    Peakman, D.2    Robinson, S.3    Henry, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.