Exclusion of uniparental disomy 15 in a prenatal diagnosis of a de novo supernumerary marker chromosome 15

被引：0
|
作者：
Soler, A [1 ]
Margarit, E [1 ]
Gomez, D [1 ]
Carrio, A [1 ]
Costa, D [1 ]
Ballesta, F [1 ]
机构：
[1] Hosp Clin Barcelona, Serv Genet, Barcelona, Spain
来源：
CYTOGENETICS AND CELL GENETICS | 1999年 / 85卷 / 1-2期
关键词：
D O I：
暂无
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
P224
引用
收藏
页码：59 / 59
页数：1
相关论文
共 50 条
  • [1] Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15
    Cotter, PD
    Ledesma, CT
    Dietz, LG
    Pusso, S
    Wohlferd, MM
    Goldberg, JD
    [J]. PRENATAL DIAGNOSIS, 1999, 19 (08) : 721 - 726
  • [2] Prenatal diagnosis of 28 de novo supernumerary marker chromosomes not deriving from chromosome 15
    Huang, B
    Ungerleider, S
    Thangavelu, M
    [J]. CYTOGENETIC AND GENOME RESEARCH, 2004, 106 (01) : 125 - 125
  • [3] Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism
    Christian, SL
    Smith, ACM
    Macha, M
    Black, SH
    Elder, FFB
    Johnson, JMP
    Resta, RG
    Surti, U
    Suslak, L
    Verp, MS
    Ledbetter, DH
    [J]. PRENATAL DIAGNOSIS, 1996, 16 (04) : 323 - 332
  • [4] Prenatal diagnosis of mosaic trisomy 15 and maternal uniparental disomy 15
    Barbieri, Veronica
    Cattani, Chiara
    Rosato, Simonetta
    Zuntini, Roberta
    Caraffi, Stefano
    Comitini, Giuseppina
    Pati, Mariangela
    Marinelli, Maria
    Garavelli, Livia
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 105 - 106
  • [5] Prenatal diagnosis of small supernumerary marker chromosome 15: A case report
    Wang, Bo
    Liu, Zhi
    Fu, Handong
    Chen, Haitao
    Xi, Jinou
    [J]. BIOMEDICAL RESEARCH-INDIA, 2017, 28 (07): : 2926 - 2928
  • [6] PRENATAL DIAGNOSIS OF A DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATING FROM CHROMOSOME 16
    Yakut, S.
    Cetin, Z.
    Simsek, M.
    Karauzum, S. B.
    Tukun, A.
    Luleci, G.
    [J]. GENETIC COUNSELING, 2009, 20 (04): : 327 - 332
  • [7] Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16
    Hengstschläger, M
    Bettelheim, D
    Drahonsky, R
    Deutinger, J
    Bernaschek, G
    [J]. PRENATAL DIAGNOSIS, 2001, 21 (06) : 477 - 480
  • [8] Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis
    von Eggeling, F
    Langer, S
    Hoppe, C
    Liehr, T
    Weise, A
    Lederer, G
    Kotzot, D
    [J]. CLINICAL GENETICS, 2003, 64 (02) : 168 - 171
  • [9] PROSPECTIVE PRENATAL DETECTION OF UNIPARENTAL DISOMY-15
    VERP, MS
    LINDGREN, V
    KNUTEL, T
    CHRISTIAN, S
    LEDBETTER, DH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1687 - 1687
  • [10] PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH
    Yakut, S.
    Cetin, Z.
    Sanhal, C.
    Karauzum, S. B.
    Karaman, B.
    Simsek, M.
    [J]. GENETIC COUNSELING, 2015, 26 (03): : 299 - 305
12345