Case of a balanced complex chromosomal rearrangement involving chromosome Y, 15, 6 and 3, 4 in an infertile male patient with cryptozoospermia

被引：0
|
作者：
Kuschmann, Malvina [1 ]
Stratis, Yvonne [1 ]
Wyrwoll, Margot Julia [2 ]
Krallmann, Claudia [3 ]
Kliesch, Sabine [3 ]
Mueller-Hofstede, Cornelie [1 ]
Tuettelmann, Frank [2 ]
Roepke, Albrecht [1 ]
机构：
[1] Univ Munster, Inst Human Genet, Munster, Germany
[2] Univ Munster, Inst Reprod Genet, Munster, Germany
[3] Univ Munster, Ctr Reprod Med & Androl, Munster, Germany
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷
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：
EP15.001
引用
收藏
页码：271 / 271
页数：1
相关论文
共 40 条
  • [21] De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: Report and review
    Batanian, JR
    Eswara, MS
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1998, 78 (01): : 44 - 51
  • [22] An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype
    Bartels, Iris
    Starke, Heike
    Argyriou, Loukas
    Sauter, Simone M.
    Zoll, Barbara
    Liehr, Thomas
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2007, 50 (02) : 133 - 138
  • [23] Complex chromosomal rearrangement involving 15q11-q13 interstitial triplication and duplication: A new case report of dysmorphic and neuropsychiatric features
    Chilakamarri, Lekha
    Mellin-Sanchez, Estrella Lizbeth
    CLINICAL CASE REPORTS, 2022, 10 (05):
  • [24] Saethre-Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7
    Zechi-Ceide, Roseli Maria
    Rodrigues, Melina Guerreiro
    Jehee, Fernanda Sarquis
    Kokitsu-Nakata, Nancy Mizue
    Passos-Bueno, Maria Rita
    Guion-Almeida, Maria Leine
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (07) : 1680 - 1685
  • [25] Infant with a de novo complex chromosomal rearrangement involving chromosomes 3, 5, 6, 7 10 and 18 and a minimum of ten breakpoints.
    Maleki, A
    Bober, M
    Tiongson, C
    Elder, F
    Wilson, K
    GENETICS IN MEDICINE, 2004, 6 (04) : 324 - 324
  • [26] Supernumerary marker chromosome with neocentromere formation within 12q2 3q24.33 after complex rearrangement involving chromosome 4 and chromosome 12
    Stratis, Yvonne
    Siebers-Renelt, Ulrike
    Wieacker, Peter
    Roepke, Albrecht
    MOLECULAR CYTOGENETICS, 2019, 12
  • [27] Characterization of a balanced complex chromosomal rearrangement carrier ascertained through a fetus with dup15q26.3 and del5p15.33: case report
    Lledo, Belen
    Antonio Ortiz, Jose
    Morales, Ruth
    Manchon, Irene
    Galan, Francisco
    Bernabeu, Andrea
    Bernabeu, Rafael
    HUMAN FERTILITY, 2013, 16 (03) : 215 - 217
  • [28] A COMPLEX 3 BREAKPOINT TRANSLOCATION INVOLVING CHROMOSOME-2, CHROMOSOME-4, AND CHROMOSOME-9 IDENTIFIED BY MEIOTIC INVESTIGATIONS OF A HUMAN MALE ASCERTAINED FOR SUBFERTILITY
    SAADALLAH, N
    HULTEN, M
    HUMAN GENETICS, 1985, 71 (04) : 312 - 320
  • [29] Analysis of a family with a partially cryptic complex chromosomal rearrangement (CCR) involving chromosomes 3, 6 and 15 by high resolution banding and FISH - Clinical description of two patients with different unbalanced translocations.
    Engels, H
    Wieczorek, D
    Viersbach, R
    Henke, B
    Schwanitz, G
    Passarge, E
    CYTOGENETICS AND CELL GENETICS, 1997, 77 (1-2): : P216 - P216
  • [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
1234