Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 → q11.23 by Array Comparative Genomic Hybridization

Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 → q11.23 by Array Comparative Genomic Hybridization

Bibliographic Details
Main Authors:	Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Chen-Chi Lee, Wayseen Wang
Format:	Article
Language:	English
Published:	Elsevier 2010-03-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455910600253

Similar Items

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)

Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)
by: Chih-Ping Chen, et al.
Published: (2013-03-01)

A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23
by: Fatih Bayrakli, et al.
Published: (2014-01-01)

A 1.37-Mb 12p11.22–p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation
by: Chih-Ping Chen, et al.
Published: (2014-03-01)

Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers
by: Roberta Lelis Dutra, et al.
Published: (2011-01-01)

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)

Arterial Hypertension in a Child with Williams-Beuren Syndrome (7q11.23 Chromosomal Deletion)
by: Cristina de Sylos, et al.
Published: (2002-08-01)

7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling
by: Maria Lisa Dentici, et al.
Published: (2020-11-01)

Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry
by: Chih-Ping Chen, et al.
Published: (2013-03-01)

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
by: Papadopoulou Anna, et al.
Published: (2011-02-01)

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
by: Papadopoulou Anna, et al.
Published: (2011-04-01)

Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion
by: Chih-Ping Chen, et al.
Published: (2021-01-01)

Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother
by: Chih-Ping Chen, et al.
Published: (2021-01-01)

A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report
by: Dalin Fu, et al.
Published: (2021-05-01)

Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1
by: Chih-Ping Chen, et al.
Published: (2015-10-01)

Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement
by: Fang Ping, et al.
Published: (2008-07-01)

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)

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)

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)

Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound
by: Chih-Ping Chen, et al.
Published: (2017-02-01)

Directly transmitted 4.5-Mb triplication of 4q12-q13.1: Prenatal diagnosis and molecular cytogenetic characterization
by: Chih-Ping Chen, et al.
Published: (2014-03-01)

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)

A Polymer Physics Investigation of the Architecture of the Murine Orthologue of the 7q11.23 Human Locus
by: Andrea M. Chiariello, et al.
Published: (2017-10-01)

Estudo citogenético da região 7q11.23 : a síndrome de Williams-Beuren /
by: Souza, Deise Helena
Published: (2003)

Estudo citogenético da região 7q11.23: a síndrome de Williams-Beuren
by: Souza, Deise Helena [UNESP]
Published: (2014)

Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2020-09-01)

An Interstitial 20q11.21 Microdeletion Causing Mild Intellectual Disability and Facial Dysmorphisms
by: Ivan Y. Iourov, et al.
Published: (2013-01-01)

Cell Models for Chromosome 20q11.21 Amplification and Drug Sensitivities in Colorectal Cancer
by: Ioannis A. Voutsadakis
Published: (2021-08-01)

Terminal 2q Deletion and Distal 15q Duplication: Prenatal Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes
by: Chih-Ping Chen, et al.
Published: (2009-12-01)

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound
by: Chih-Ping Chen, et al.
Published: (2017-12-01)

Clinical Characterization of a 6-Year-Old Patient with Autism and Two Adjacent Duplications on 10q11.22q11.23. A Case Report
by: Giovanna Tritto, et al.
Published: (2021-06-01)

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)

Optic nerve coloboma as extension of the phenotype of 22q11.23 duplication syndrome: a case report
by: Claudia Valencia-Peña, et al.
Published: (2020-08-01)

A rare case of acute myeloid leukemia with ARHGEF12 (LARG, 11q23.3) and MAPRE1 (EB1, 20q11.21) fusion gene in an elderly patient
by: Macarie Ioan, et al.
Published: (2020-01-01)

Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
by: Yu-Ling Kuo, et al.
Published: (2014-06-01)

Evaluation of loss of heterozygosity of chromosome 22q11.21 region in patients with congenital heart diseases
by: Eman G. Behiry, et al.
Published: (2018-12-01)

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report
by: Domenico Dell’Edera, et al.
Published: (2021-04-01)

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
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)

Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound
by: Chih-Ping Chen, et al.
Published: (2020-07-01)