Cargando…

The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature

ABSTRACT: The clinical utility of microarray technologies when used in the context of prenatal diagnosis lies in the technology's ability to detect submicroscopic copy number changes that are associated with clinically significant outcomes. We have carried out a systematic review of the literat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Callaway, Jonathan L A, Shaffer, Lisa G, Chitty, Lyn S, Rosenfeld, Jill A, Crolla, John A
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BlackWell Publishing Ltd 2013
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285999/ https://www.ncbi.nlm.nih.gov/pubmed/23983223 http://dx.doi.org/10.1002/pd.4209

Ejemplares similares

Cytogenetic microarray in prenatal and postnatal diagnosis
por: Phadke, Shubha
Publicado: (2014)

Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis
por: Zhang, Jinman, et al.
Publicado: (2021)

Evaluation of a Novel Assay for Detection of the Fetal Marker RASSF1A: Facilitating Improved Diagnostic Reliability of Noninvasive Prenatal Diagnosis
por: White, Helen E., et al.
Publicado: (2012)

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

Prenatal and postnatal echocardiography in NT fetuses with normal karyotype
por: Emami-Moghaddam, Abdolrahman, et al.
Publicado: (2019)

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
por: Shi, Xiaomei, et al.
Publicado: (2021)

Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed‐methods systematic review
por: Harding, Eleanor, et al.
Publicado: (2020)

What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing
por: Peter, Michelle, et al.
Publicado: (2021)

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

Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis
por: Guo, Huan, et al.
Publicado: (2023)

Karyotype analysis of seven species of the tribe Lophiohylini (Hylinae, Hylidae, Anura), with conventional and molecular cytogenetic techniques
por: Gruber, Simone Lilian, et al.
Publicado: (2012)

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype
por: Wu, Xiaoqing, et al.
Publicado: (2020)

Cytogenetic Karyotype Analysis in Selected Species of the Erinaceidae Family
por: Grzesiakowska, Anna, et al.
Publicado: (2019)

The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing
por: Riedijk, Sam, et al.
Publicado: (2014)

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
por: Shaffer, Lisa G, et al.
Publicado: (2012)

First cytogenetic analysis of Ichthyoelephas humeralis (Günther, 1860) by conventional and molecular methods with comments on the karyotypic evolution in Prochilodontidae
por: Tursellino, Mauro Nirchio, et al.
Publicado: (2016)

Cytogenetic analyses in Trinomys (Echimyidae, Rodentia), with description of new karyotypes
por: Araújo, Naiara Pereira, et al.
Publicado: (2018)

Cytogenetic Evidence for Sex Chromosomes and Karyotype Evolution in Anguimorphan Lizards
por: Augstenová, Barbora, et al.
Publicado: (2021)

CytoGPS: a web-enabled karyotype analysis tool for cytogenetics
por: Abrams, Zachary B, et al.
Publicado: (2019)

First cytogenetic data on Afrotropical lutefishes (Citharinidae) in the light of karyotype evolution in Characiformes
por: Simanovsky, Sergey A., et al.
Publicado: (2022)

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
por: Su, Linjuan, et al.
Publicado: (2019)

Cytogenetic Analysis of the Bimodal Karyotype of the Common European Adder, Vipera berus (Viperidae)
por: Spangenberg, Victor, et al.
Publicado: (2022)

Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies
por: Wang, Jin, et al.
Publicado: (2022)

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)

Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?
por: Karampetsou, Evangelia, et al.
Publicado: (2014)

Virtual karyotyping with SNP microarrays reduces uncertainty in the diagnosis of renal epithelial tumors
por: Hagenkord, Jill M, et al.
Publicado: (2008)

Role of conventional cytogenetics in sequential karyotype analysis of myelodysplastic syndrome: a patient with der(1;7)(q10;p10)
por: França, Ivo Gabriel da Frota, et al.
Publicado: (2019)

Epidemiology of fetal cerebral ventriculomegaly and evaluation of chromosomal microarray analysis versus karyotyping for prenatal diagnosis in a Chinese hospital
por: Yi, Jun-Ling, et al.
Publicado: (2019)

PB1914: CYTOGENETIC FINDINGS IN 18 CHILDREN WITH MYELODYSPLASTIC SYNDROMES BY KARYOTYPIC AND FISH ANALYSIS
por: Manola, K., et al.
Publicado: (2022)

Non-invasive prenatal diagnosis (NIPD): how analysis of cell-free DNA in maternal plasma has changed prenatal diagnosis for monogenic disorders
por: Hanson, Britt, et al.
Publicado: (2022)

Partial Molar Pregnancy With Normal Karyotype
por: Al Ghadeer, Hussain A, et al.
Publicado: (2022)

Karyotypic conservatism in five species of Prochilodus (Characiformes, Prochilodontidae) disclosed by cytogenetic markers
por: Voltolin, Tatiana Aparecida, et al.
Publicado: (2013)

Advances in cytogenetics of Brazilian rodents: cytotaxonomy, chromosome evolution and new karyotypic data
por: Di-Nizo, Camilla Bruno, et al.
Publicado: (2017)

A qualitative study looking at informed choice in the context of non‐invasive prenatal testing for aneuploidy
por: Lewis, Celine, et al.
Publicado: (2016)

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes
por: Slovak, Marilyn L, et al.
Publicado: (2010)

RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy
por: Lo, Kitty K., et al.
Publicado: (2014)

Cyclopia syndrome with normal karyotype
por: Banerjee, Sayan, et al.
Publicado: (2020)

Offering non‐invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
por: Lewis, Celine, et al.
Publicado: (2017)

Chromosome painting in three-toed sloths: a cytogenetic signature and ancestral karyotype for Xenarthra
por: Azevedo, Nathália F, et al.
Publicado: (2012)

A First Glimpse of Wild Lupin Karyotype Variation As Revealed by Comparative Cytogenetic Mapping
por: Susek, Karolina, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_sr3qiupdvt8dkh2ejgfjjc793f