메뉴 건너뛰기




Volumn 49, Issue 2, 2010, Pages 188-191

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18

Author keywords

Chromosome 17; Chromosome 18; Marker chromosome 18; Prenatal diagnosis; Reciprocal translocation; Small supernumerary marker chromosome

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 17; CHROMOSOME 17Q; CHROMOSOME 18; CHROMOSOME 18Q; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FEMALE; FETUS; GENETIC COUNSELING; GESTATIONAL AGE; HUMAN; KARYOTYPE; MATERNAL AGE; PRENATAL DIAGNOSIS; SUPERNUMERARY CHROMOSOME;

EID: 77955574157     PISSN: 10284559     EISSN: 10284559     Source Type: Journal    
DOI: 10.1016/S1028-4559(10)60039-3     Document Type: Article
Times cited : (8)

References (16)
  • 1
    • 7944237049 scopus 로고    scopus 로고
    • Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature
    • Chen CP, Lin CC, Li YC, et al. Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature. Prenat Diagn 2004, 24:767-773.
    • (2004) Prenat Diagn , vol.24 , pp. 767-773
    • Chen, C.P.1    Lin, C.C.2    Li, Y.C.3
  • 2
    • 33750555572 scopus 로고    scopus 로고
    • Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype
    • Lin CC, Hsieh YY, Wang CH, et al. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype. Prenat Diagn 2006, 26:898-902.
    • (2006) Prenat Diagn , vol.26 , pp. 898-902
    • Lin, C.C.1    Hsieh, Y.Y.2    Wang, C.H.3
  • 3
    • 73449091212 scopus 로고    scopus 로고
    • Prenatal diagnosis of mos45,X/46,X,+ mar in a fetus with normal male external genitalia and a literature review
    • Chien SC, Chen CP, Lin CC, Huang LC, Hsieh CT, Tsai FJ Prenatal diagnosis of mos45,X/46,X,+ mar in a fetus with normal male external genitalia and a literature review. Taiwan J Obstet Gynecol 2009, 48:292-295.
    • (2009) Taiwan J Obstet Gynecol , vol.48 , pp. 292-295
    • Chien, S.C.1    Chen, C.P.2    Lin, C.C.3    Huang, L.C.4    Hsieh, C.T.5    Tsai, F.J.6
  • 4
    • 66449091845 scopus 로고    scopus 로고
    • Handling small supernumerary marker chromosomes in prenatal diagnostics
    • Liehr T, Ewers E, Kosyakova N, et al. Handling small supernumerary marker chromosomes in prenatal diagnostics. Expert Rev Mol Diagn 2009, 9:317-324.
    • (2009) Expert Rev Mol Diagn , vol.9 , pp. 317-324
    • Liehr, T.1    Ewers, E.2    Kosyakova, N.3
  • 5
    • 4344625842 scopus 로고    scopus 로고
    • Small supernumerary marker chromosomes (sSMC) in humans
    • Liehr T, Claussen U, Starke H Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004, 107:55-67.
    • (2004) Cytogenet Genome Res , vol.107 , pp. 55-67
    • Liehr, T.1    Claussen, U.2    Starke, H.3
  • 6
    • 27644520395 scopus 로고    scopus 로고
    • Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation
    • Liehr T, Mrasek K, Weise A, et al. Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation. Cytogenet Genome Res 2006, 112:23-34.
    • (2006) Cytogenet Genome Res , vol.112 , pp. 23-34
    • Liehr, T.1    Mrasek, K.2    Weise, A.3
  • 7
    • 84934438485 scopus 로고    scopus 로고
    • Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics
    • Liehr T Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics. Methods Mol Biol 2008, 444:27-38.
    • (2008) Methods Mol Biol , vol.444 , pp. 27-38
    • Liehr, T.1
  • 8
    • 34248544965 scopus 로고    scopus 로고
    • Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics
    • Liehr T, Weise A Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 2007, 19:719-731.
    • (2007) Int J Mol Med , vol.19 , pp. 719-731
    • Liehr, T.1    Weise, A.2
  • 11
    • 10744232485 scopus 로고    scopus 로고
    • Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification
    • Starke H, Nietzel A, Weise A, et al. Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 2003, 114:51-67.
    • (2003) Hum Genet , vol.114 , pp. 51-67
    • Starke, H.1    Nietzel, A.2    Weise, A.3
  • 12
    • 1942491171 scopus 로고    scopus 로고
    • Characterization of small marker chromosomes (SMC) by recently developed molecular cytogenetic approaches
    • Liehr T, Nietzel A, Starke H, et al. Characterization of small marker chromosomes (SMC) by recently developed molecular cytogenetic approaches. J Assoc Genet Technol 2003, 29:5-10.
    • (2003) J Assoc Genet Technol , vol.29 , pp. 5-10
    • Liehr, T.1    Nietzel, A.2    Starke, H.3
  • 13
    • 47649097067 scopus 로고    scopus 로고
    • Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature
    • Manvelyan M, Riegel M, Santos M, et al. Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature. Int J Mol Med 2008, 21:705-714.
    • (2008) Int J Mol Med , vol.21 , pp. 705-714
    • Manvelyan, M.1    Riegel, M.2    Santos, M.3
  • 14
    • 33847369009 scopus 로고    scopus 로고
    • Array painting using microdissected chromosomes to map chromosomal breakpoints
    • Backx L, Van Esch H, Melotte C, et al. Array painting using microdissected chromosomes to map chromosomal breakpoints. Cytogenet Genome Res 2007, 116:158-166.
    • (2007) Cytogenet Genome Res , vol.116 , pp. 158-166
    • Backx, L.1    Van Esch, H.2    Melotte, C.3
  • 15
    • 34249071991 scopus 로고    scopus 로고
    • New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank
    • Tönnies H, Pietrzak J, Bocian E, et al. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank. J Histochem Cytochem 2007, 55:651-660.
    • (2007) J Histochem Cytochem , vol.55 , pp. 651-660
    • Tönnies, H.1    Pietrzak, J.2    Bocian, E.3
  • 16
    • 40749147287 scopus 로고    scopus 로고
    • Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues
    • Baldwin EL, May LF, Justice AN, Martin CL, Ledbetter DH Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues. Am J Hum Genet 2008, 82:398-410.
    • (2008) Am J Hum Genet , vol.82 , pp. 398-410
    • Baldwin, E.L.1    May, L.F.2    Justice, A.N.3    Martin, C.L.4    Ledbetter, D.H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.