Cover Image

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 8

Objective: To present prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 8 by multiplex ligation-dependent probe amplification (MLPA), fluorescence in situ hybridization (FISH), spectral karyotyping (SKY) and array...

Full description

Saved in:

Bibliographic Details
Main Authors:	Chih-Ping Chen (Author), Ming Chen (Author), Tsang-Ming Ko (Author), Gwo-Chin Ma (Author), Fuu-Jen Tsai (Author), Ming-Song Tsai (Author), Pei-Chen Wu (Author), Chen-Chi Lee (Author), Li-Feng Chen (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2010-12-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21
by: Chih-Ping Chen, et al.
Published: (2010)

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22
by: Chih-Ping Chen, et al.
Published: (2010)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
by: Chih-Ping Chen, et al.
Published: (2011)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3
by: Chih-Ping Chen, et al.
Published: (2019)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
by: Chih-Ping Chen, et al.
Published: (2017)

Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome
by: Chih-Ping Chen, et al.
Published: (2011)

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated With a Reciprocal Translocation Involving Chromosomes 17 And 18
by: Chih-Ping Chen, et al.
Published: (2010)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21
by: Chih-Ping Chen, et al.
Published: (2017)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2
by: Chih-Ping Chen, et al.
Published: (2017)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15
by: Chih-Ping Chen, et al.
Published: (2014)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11
by: Chih-Ping Chen, et al.
Published: (2017)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2
by: Chih-Ping Chen, et al.
Published: (2012)

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions
by: Chih-Ping Chen, et al.
Published: (2017)

Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
by: Chih-Ping Chen, et al.
Published: (2010)

Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome
by: Chih-Ping Chen, et al.
Published: (2016)

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)

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome
by: Chih-Ping Chen, et al.
Published: (2021)

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9
by: Chih-Ping Chen, et al.
Published: (2017)

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)

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)

Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10)
by: Chih-Ping Chen, et al.
Published: (2022)

Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation
by: Chih-Ping Chen, et al.
Published: (2011)

A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
by: Chih-Ping Chen, et al.
Published: (2011)

Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay
by: Chih-Ping Chen, et al.
Published: (2016)

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)

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)

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)

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)

Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p
by: Chih-Ping Chen, et al.
Published: (2011)

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 associated with congenital hypoplasia of the tongue and review of the literature
by: Hui-Yuan Shao, et al.
Published: (2020)

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

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)

Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
by: Chih-Ping Chen, et al.
Published: (2011)

Prenatal diagnosis and molecular cytogenetic characterization of three chromosomal abnormalities with favorable outcomes
by: Qiuqing Chen, et al.
Published: (2020)

Retrospectively investigating the 12-year experience of prenatal diagnosis of small supernumerary marker chromosomes through array comparative genomic hybridization
by: Min-Hui Huang, et al.
Published: (2019)

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

Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization
by: Chih-Ping Chen, et al.
Published: (2010)

Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study
by: Shuang Hu, et al.
Published: (2023)

Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3)
by: Chih-Ping Chen, et al.
Published: (2011)