Interstitial 4q deletion associated with a mosaic complementary supernumerary marker chromosome in prenatal diagnosis

被引:0
|
作者
Capalbo, Anna [1 ]
Sinibaldi, Lorenzo [1 ]
Bernardini, Laura [1 ]
Spasari, Iolanda [1 ]
Mancuso, Brunella [2 ]
Maggi, Eugenio [1 ]
Novelli, Antonio [1 ]
机构
[1] IRCCS, Mendel Lab, Fdn Casa Sollievo Sofferenza, Foggia, Italy
[2] Annunziata Hosp, Genet Unit, Cosenza, Italy
基金
英国惠康基金;
关键词
ARRAY-CGH; STATURE;
D O I
10.1002/pd.4105
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:782 / 796
页数:15
相关论文
共 50 条
  • [31] Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
    Chen, Chih-Ping
    Chen, Ming
    Su, Yi-Ning
    Tsai, Fuu-Jen
    Chern, Schu-Rern
    Wu, Pei-Chen
    Chen, Wen-Lin
    Chen, Li-Feng
    Pan, Chen-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2011, 50 (02): : 188 - 195
  • [32] Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16
    Hengstschläger, M
    Bettelheim, D
    Drahonsky, R
    Deutinger, J
    Bernaschek, G
    PRENATAL DIAGNOSIS, 2001, 21 (06) : 477 - 480
  • [33] Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH
    Gole, LA
    Biswas, A
    PRENATAL DIAGNOSIS, 2005, 25 (01) : 73 - 78
  • [34] Prenatal diagnosis of de novo mosaic deletion 13q associated with multiple abnormalities
    Widschwendter, A
    Riha, K
    Duba, HC
    Kreczy, A
    Marth, C
    Schwärzler, P
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2002, 19 (04) : 396 - 399
  • [35] Could be a supernumerary marker chromosome in mosaic associated with pregnancy loss? A case report
    Apostol, P.
    Cristea, M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 948 - 949
  • [36] A CLOSELY LINKED DNA MARKER FOR FACIOSCAPULOHUMERAL DISEASE ON CHROMOSOME 4Q
    UPADHYAYA, M
    LUNT, PW
    SARFARAZI, M
    BROADHEAD, W
    DANIELS, J
    OWEN, M
    HARPER, PS
    JOURNAL OF MEDICAL GENETICS, 1991, 28 (10) : 665 - 671
  • [37] Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly
    Chen, CP
    Lee, CC
    Chen, LF
    Chuang, CY
    Jan, SW
    Chen, BF
    JOURNAL OF MEDICAL GENETICS, 1997, 34 (09) : 777 - 778
  • [38] Implications of Prenatal Diagnosis of the Fetus With Both Interstitial Deletion and a Small Marker Ring Originating From Chromosome 5
    Ohashi, Hiroyasu
    Suzumori, Kaoru
    Chisaka, Yasushi
    Sonta, Shinichi
    Kobayashi, Tomoko
    Aoki, Yoko
    Matsubara, Yoichi
    Sone, Michiko
    Shaffer, Lisa G.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (01) : 192 - 196
  • [39] Prenatal diagnosis of a mosaic marker chromosome 14 by spectral karyotyping.
    Laundon, CH
    Ning, Y
    Ried, T
    Buchanan, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A156 - A156
  • [40] Cytogenomic characterization of a complex small supernumerary marker chromosome leading to partial 4q and 21q duplications: clinical implication and review of the literature
    Bellucco, F. T.
    Fock, R. A.
    Oliveira-, H. R., Jr.
    Perez, A. B.
    Melaragno, M. I.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 985 - 985