Detection of Balanced Homologous Acrocentric Rearrangement REA(14Q14Q) and Low-Grade X-Chromosome Mosaicism in a Couple With Repeated Pregnancy Losses

Detection of Balanced Homologous Acrocentric Rearrangement REA(14Q14Q) and Low-Grade X-Chromosome Mosaicism in a Couple With Repeated Pregnancy Losses

Bibliographic Details
Main Authors:	Chih-Ping Chen, Schu-Rern Chern, Chia-Hsun Wu, Fuu-Jen Tsai, Pei-Chen Wu, Wayseen Wang
Format:	Article
Language:	English
Published:	Elsevier 2010-06-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Online Access:	http://www.sciencedirect.com/science/article/pii/S102845591060054X

Similar Items

Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses
by: Chih-Ping Chen, et al.
Published: (2012-12-01)

Down Syndrome Due to Unbalanced Homologous Acrocentric Rearrangements and its Recurrence in Subsequent Pregnancies: Prenatal Diagnosis by Amniocentesis
by: Chih-Ping Chen, et al.
Published: (2009-12-01)

Unbalanced and Balanced Heterologous Acrocentric Rearrangements Involving Chromosome 21 at Amniocentesis
by: Chih-Ping Chen, et al.
Published: (2010-03-01)

Unbalanced and Balanced Acrocentric Rearrangements Involving Chromosomes Other Than Chromosome 21 at Amniocentesis
by: Chih-Ping Chen, et al.
Published: (2009-12-01)

Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader–Willi syndrome
by: Chih-Ping Chen, et al.
Published: (2021-03-01)

Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry
by: Chih-Ping Chen, et al.
Published: (2013-03-01)

Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism
by: Chih-Ping Chen, et al.
Published: (2021-01-01)

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin
by: Chih-Ping Chen, et al.
Published: (2020-09-01)

Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review
by: Chih-Ping Chen, et al.
Published: (2019-11-01)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review
by: Chih-Ping Chen, et al.
Published: (2017-08-01)

Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly
by: Chih-Ping Chen, et al.
Published: (2011-06-01)

De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: Prenatal diagnosis and molecular cytogenetic characterization
by: Chih-Ping Chen, et al.
Published: (2013-09-01)

Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review
by: Chih-Ping Chen, et al.
Published: (2013-09-01)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia
by: Chih-Ping Chen, et al.
Published: (2020-11-01)

Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021-07-01)

Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication
by: Chih-Ping Chen, et al.
Published: (2016-08-01)

Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2015-02-01)

Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2013-09-01)

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2011-06-01)

Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes
by: Chih-Ping Chen, et al.
Published: (2021-03-01)

Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of 21q22.3
by: Chih-Ping Chen, et al.
Published: (2012-03-01)

Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis
by: Chih-Ping Chen, et al.
Published: (2017-04-01)

Partial Trisomy 10q (10q25.1 →qter) and Partial Monosomy 13q (13q34→qter) Presenting With Fetal Pyelectasis: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization
by: Chih-Ping Chen, et al.
Published: (2010-12-01)

Molecular and Cytogenetic Characterization of de novo Acrocentric Rearrangements in Humans
by: Shaffer, Lisa Gail
Published: (1990)

Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 → q11.23 by Array Comparative Genomic Hybridization
by: Chih-Ping Chen, et al.
Published: (2010-03-01)

Prognostic value of 13q14 deletion and IgH 14q32 rearrangement by interphase fluorescence in situ hybridization in patients with multiple myeloma
by: Nevine A Kassem, et al.
Published: (2014-01-01)

Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects
by: Chih-Ping Chen, et al.
Published: (2021-03-01)

Trisomy 13 Mosaicism Associated With Cyclopia and Cystic Hygroma
by: Chih-Ping Chen, et al.
Published: (2009-12-01)

Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality
by: Chih-Ping Chen, et al.
Published: (2017-04-01)

Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q
by: Ana I. Vásquez-Velásquez, et al.
Published: (2016-04-01)

Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): Array comparative genomic hybridization characterization and literature review
by: Chih-Ping Chen, et al.
Published: (2012-12-01)

Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects
by: Chih-Ping Chen, et al.
Published: (2019-09-01)

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities
by: Chih-Ping Chen, et al.
Published: (2016-12-01)

Prenatal Diagnosis of 46,XX,der(13;21)(q10;q10),+21 and Transient Abnormal Myelopoiesis in a Fetus with Hepatosplenomegaly and Spontaneous Resolution of Fetal Ascites
by: Chih-Ping Chen, et al.
Published: (2009-03-01)

Chromosome Duplication (14q) and The Genotype Phenotype Correlation
by: Ariane Sadr-Nabavi, et al.
Published: (2014-04-01)

Characterisation of the atopy locus on chromosome 13q14
by: Anderson, Gavin George
Published: (2001)

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot
by: Chih-Ping Chen, et al.
Published: (2016-04-01)

Fragility in the 14q21q translocation region
by: Stacy R. Denison, et al.
Published: (2002-01-01)

Prenatal Diagnosis and Molecular Analysis of Trisomy 13 Mosaicism
by: Chih-Ping Chen, et al.
Published: (2009-09-01)

Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound
by: Chih-Ping Chen, et al.
Published: (2020-09-01)

Cannot write session to /tmp/vufind_sessions/sess_s07v4jbjelgr6sbdj9pl6ugas9