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
  • [21] Prenatal diagnosis of small supernumerary marker chromosome 15: A case report
    Wang, Bo
    Liu, Zhi
    Fu, Handong
    Chen, Haitao
    Xi, Jinou
    BIOMEDICAL RESEARCH-INDIA, 2017, 28 (07): : 2926 - 2928
  • [22] Rare proximal interstitial deletion of chromosome 4q, del(4)(q13.2q21.22):: New case and comparison with the literature
    Eggermann, K
    Bergmann, C
    Heil, I
    Eggermann, T
    Zerres, K
    Schüler, HM
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 134A (02) : 226 - 228
  • [23] Complex Small Supernumerary Marker Chromosome Leading to Partial 4q/21q Duplications: Clinical Implication and Review of the Literature
    Bellucco, Fernanda T.
    Fock, Rodrigo A.
    de Oliveira-Junior, Helio R.
    Perez, Ana B.
    Melaragno, Maria I.
    CYTOGENETIC AND GENOME RESEARCH, 2018, 156 (04) : 173 - 178
  • [24] 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.
    GENETIC COUNSELING, 2009, 20 (04): : 327 - 332
  • [25] Prenatal diagnosis of mosaic ring chromosome 4
    Chen, Chih-Ping
    Hsu, Chin-Yuan
    Tzen, Chin-Yuan
    Lee, Chen-Chi
    Chen, Wen-Lin
    Chen, Li-Feng
    Wang, Wayseen
    PRENATAL DIAGNOSIS, 2007, 27 (05) : 485 - 487
  • [26] DE NOVO MOSAIC MARKER CHROMOSOME DETECTED IN PRENATAL DIAGNOSIS
    Yuregir, Ozge Ozalp
    Yilmaz, Zerrin
    Sahin, Feride Iffet
    Bilezikci, Banu
    Yanik, Filiz
    TURKISH JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2008, 5 (01) : 17 - 21
  • [27] "Opitz C Syndrome and Pseudohypoaldosteronism" Is Caused by a Chromosome 4q Deletion
    de Ravel, Thomy
    Balikova, Irina
    Van Driessche, Jozef
    Vermeesch, Joris
    Fryns, Jean-Pierre
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (06) : 1315 - 1316
  • [28] Ophthalmic Features in a Dysmorphic Boy with Chromosome 4q Deletion and Duplication
    Parentin, Fulvio
    Fabretto, Antonella
    Benussi, Daniela Gambel
    Petix, Vincenzo
    Marchetti, Federico
    Dalpra, Leda
    Redaelli, Serena
    Pensiero, Stefano
    Pecile, Vanna
    OPHTHALMIC GENETICS, 2009, 30 (02) : 103 - 105
  • [29] Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion
    Oh, DC
    Min, JY
    Lee, MH
    Kim, YM
    Park, SY
    Won, HS
    Kim, IK
    Lee, YH
    Yoo, SJ
    Ryu, HM
    JOURNAL OF KOREAN MEDICAL SCIENCE, 2002, 17 (01) : 125 - 128
  • [30] Terminal deletion of 4q in a child with ring chromosome 4 and minor malformations
    Barrionuevo Gonzalez, Marta
    Ramirez Fernandez, Joaquin
    Garcia Garcia, Blanca
    Alvarez Blanco, Ma Jose
    Varela Sanz, Luis Antonio
    Coca Martin, Carmen
    Villalon Villaroel, Concepcion
    Garcia Galloway, Eva
    Miguel Garcia-Sagredo, Jose
    CHROMOSOME RESEARCH, 2011, 19 : S94 - S95