Cargando…

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray

This study examined the molecular characterization of a prenatal case with true fetal mosaicism of small supernumerary marker chromosome 16 (sSMC(16)). A 41-year-old female underwent amniocentesis at 19 weeks of gestation due to advanced maternal age. Chromosomal analysis for cultured amniocytes rev...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yao, Tien-Yu, Wu, Wan-Ju, Law, Kim-Seng, Lee, Mei-Hui, Chang, Shun-Ping, Lee, Dong-Jay, Lin, Wen-Hsiang, Chen, Ming, Ma, Gwo-Chin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391486/ https://www.ncbi.nlm.nih.gov/pubmed/34441391 http://dx.doi.org/10.3390/diagnostics11081457

Ejemplares similares

Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis
por: Xue, Huili, et al.
Publicado: (2019)

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis
por: Xue, Huili, et al.
Publicado: (2020)

Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
por: Yang, Yang, et al.
Publicado: (2023)

Chromosomal mosaicism detected by karyotyping and chromosomal microarray analysis in prenatal diagnosis
por: Zhang, Yi, et al.
Publicado: (2020)

The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis
por: Hao, MengZhe, et al.
Publicado: (2020)

Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes
por: Liehr, Thomas, et al.
Publicado: (2010)

Molecular cytogenetic characterization of a mosaic small supernumerary marker chromosome derived from chromosome Y in an azoospermic male: A case report
por: Zhang, Hongguo, et al.
Publicado: (2019)

Characterization of prenatally detected small Supernumerary Marker Chromosomes (sSMC) by molecular cytogenetic technique: FISH
por: Patel, Bhumi, et al.
Publicado: (2014)

Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics
por: Klein, Elisabeth, et al.
Publicado: (2012)

Cellular consequences of small supernumerary marker chromosome derived from chromosome 12: mosaicism in daughter and father
por: Freitas, M.O., et al.
Publicado: (2022)

Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in foetuses with ventriculomegaly
por: Wang, Jiamin, et al.
Publicado: (2020)

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
por: Lebedev, Igor N., et al.
Publicado: (2021)

Small supernumerary marker chromosomes derived from chromosome 14 and/or 22
por: Liehr, Thomas, et al.
Publicado: (2021)

Small supernumerary marker chromosomes – an update
por: Liehr, Thomas
Publicado: (2014)

Be careful with small supernumerary marker chromosomes!
por: Rodríguez, Laura
Publicado: (2023)

Application of chromosome microarray analysis in prenatal diagnosis
por: Xia, Mingjing, et al.
Publicado: (2020)

Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization
por: Tsuchiya, Karen D, et al.
Publicado: (2008)

Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p
por: Demily, Caroline, et al.
Publicado: (2014)

Combined Use of Cytogenetic and Molecular Methods in Prenatal Diagnostics of Chromosomal Abnormalities
por: Stomornjak-Vukadin, Meliha, et al.
Publicado: (2015)

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis
por: Liu, Xijing, et al.
Publicado: (2022)

Complex small supernumerary marker chromosomes – an update
por: Liehr, Thomas, et al.
Publicado: (2013)

Discovery of Supernumerary B Chromosomes in Drosophila melanogaster
por: Bauerly, Elisabeth, et al.
Publicado: (2014)

Evolution, Composition and Regulation of Supernumerary B Chromosomes
por: Houben, Andreas, et al.
Publicado: (2019)

Effects of sex chromosome dosage on corpus callosum morphology in supernumerary sex chromosome aneuploidies
por: Wade, Benjamin S C, et al.
Publicado: (2014)

First case of two supernumerary markers derived from chromosome 5 and chromosome 8
por: Giansante, Roberta, et al.
Publicado: (2022)

THE EFFECT OF MATERNAL AGE ON CHROMOSOMAL MOSAICISM: AN ANALYSIS BY CHROMOSOME TYPE AND MOSAIC RESULT
por: Reich, Jenna, et al.
Publicado: (2020)

Whole Exome Sequencing Facilitated the Identification of a Mosaic Small Supernumerary Marker Chromosome (sSMC)
por: Xing, Huan-xia, et al.
Publicado: (2021)

The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts
por: Novik, Veronica, et al.
Publicado: (2014)

Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalities
por: Song, Tingting, et al.
Publicado: (2020)

The Incidence of Mosaicism for Individual Chromosome in Human Blastocysts Is Correlated With Chromosome Length
por: Chuang, Tzu-Hsuan, et al.
Publicado: (2021)

Confined placental mosaicism: implications for fetal chromosomal analysis using microarray comparative genomic hybridization
por: Karampetsou, Evangelia, et al.
Publicado: (2014)

Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them
por: Liehr, Thomas, et al.
Publicado: (2008)

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report
por: VAHIDI MEHRJARDI, Mohammad Yahya, et al.
Publicado: (2016)

Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7
por: Tsai, Li-Ping, et al.
Publicado: (2011)

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis
por: Armengol, Lluís, et al.
Publicado: (2011)

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?
por: Miny, Peter, et al.
Publicado: (2013)

Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism
por: Zhang, Min, et al.
Publicado: (2022)

Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis
por: Grati, Francesca Romana
Publicado: (2014)

Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis
por: Yu, Mullin Ho Chung, et al.
Publicado: (2021)

Small supernumerary marker chromosomes and their correlation with specific syndromes
por: Jafari-Ghahfarokhi, Hamideh, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_a4rqjb73pklcuubi63tsg8absp