Trisomy 4q22.3-q35.2 in a patient with additional material in 16q24 due to a de novo chromosomal rearrangement

被引:0
|
作者
Gonzalez-Huerta, L. [1 ]
Rivera-Vega, M. [1 ]
Valdes-Miranda, J. [1 ]
Perez-Cabrera, A. [1 ]
Cuevas-Covarrubias, S. [2 ]
机构
[1] Hosp Gen Mexico City, Genet, Mexico City, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Genet, Mexico City, DF, Mexico
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P11.122B
引用
收藏
页码:507 / 508
页数:2
相关论文
共 50 条
  • [21] Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q
    Vasquez-Velasquez, Ana I.
    Rivera, Horacio
    Castro, Ana G.
    Jaloma-Cruz, Ana R.
    Juarez, Clara I.
    Lara-Navarro, Irving J.
    Cordova-Fletes, Carlos
    Mendoza-Perez, Paul
    Garcia-Ortiz, Jose E.
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (02): : 275 - 280
  • [22] De novo Copy Number Losses of Chromosomes 2q22.3q23.2 and 5q11.2q12.2 in a Female Patient with Clinical Features of Angelman Syndrome: A Case Report
    Chaubey, A. D.
    Bartel, F.
    Skinner, S. A.
    DuPont, B. R.
    CYTOGENETIC AND GENOME RESEARCH, 2012, 136 (04) : 327 - 327
  • [23] Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q)
    Mercier, S
    Fellmann, F
    Cattin, J
    Bresson, JL
    PRENATAL DIAGNOSIS, 1996, 16 (11) : 1046 - 1050
  • [24] Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation
    Velinov, M
    Gu, H
    Yeboa, K
    Warburton, D
    Tubo, T
    Dhuper, S
    Lanter, S
    Delprino, D
    Kupchik, G
    Jenkins, EC
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 107 (04): : 330 - 333
  • [25] Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q
    Martin-De Saro, Monica D.
    Valdes-Miranda, Juan M.
    Plaza-Benhumea, Lautaro
    Perez-Cabrera, Adrian
    Gonzalez-Huerta, Luz M.
    Guevara-Yanez, Roberto
    Cuevas-Covarrubias, Sergio A.
    CYTOGENETIC AND GENOME RESEARCH, 2015, 147 (2-3) : 124 - 129
  • [26] A case of de novo translocation 16;21: Trisomy 16q phenotype and origin of the aberration.
    Eggermann, T
    Kolin-Gerresheim, I
    Gerresheim, F
    Schwanitz, G
    ANNALES DE GENETIQUE, 1998, 41 (04): : 205 - 208
  • [27] Trisomy 16q in a female newborn with a de novo X;16 translocation and hypoplastic left heart
    Bacino, CA
    Lee, B
    Spikes, AS
    Shaffer, LG
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 82 (02): : 128 - 131
  • [28] Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH
    Petek, E
    Köstl, G
    Mutz, I
    Wagner, K
    Kroisel, PM
    CLINICAL DYSMORPHOLOGY, 2000, 9 (01) : 55 - 57
  • [29] Clinical and Prognostic Features in a Young Adult Patient with de novo Myelodysplastic Syndrome Presenting t(11;16)(q23;q24)
    Lovatel, Viviane Lamim
    Otero, Luize
    Orlando, Ercole Pietro
    Diniz, Claudia
    Praxedes Lusis, Monica Kopischitz
    Fernandez, Teresa de Souza
    MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES, 2022, 14
  • [30] Complex De Novo Chromosomal Rearrangement at 15q11-q13 Involving an Intrachromosomal Triplication in a Patient with a Severe Neuropsychological Phenotype: Clinical Report and Review of the Literature
    Castronovo, Chiara
    Crippa, Milena
    Bestetti, Ilaria
    Rusconi, Daniela
    Russo, Silvia
    Larizza, Lidia
    Sangermani, Roberto
    Bonati, Maria Teresa
    Finelli, Palma
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (01) : 221 - 230