Literature DB >> 16906550

Array comparative genomic hybridization analysis in first-trimester spontaneous abortions with 'normal' karyotypes.

Osamu Shimokawa1, Naoki Harada, Noriko Miyake, Kanako Satoh, Takeshi Mizuguchi, Norio Niikawa, Naomichi Matsumoto.   

Abstract

Array comparative genomic hybridization (array CGH) analysis was conducted in chorionic villous samples from 20 first-trimester spontaneous abortions with G-banding normal chromosomes. A microarray, containing 2,173 BAC clones and covering the whole genome with a 1.5-Mb resolution, was constructed and used in the analysis. Two deletions were identified: a 1.4-Mb deletion at 3p26.2-p26.3 and a 13.7-Mb deletion at 13q32.3-qter. Reexamination of chromosome preparations from the sample with the 13.7-Mb deletion documented a mixture of cells with the 13q- chromosome and those with 46,XX chromosomes, the latter of which are likely to have been derived from contaminating decidual cells. This left the 1.4-Mb 3p deletion as the only instance with submicroscopic imbalance detected, giving a frequency of 1 in 19 (5%) G-banding normal abortions.

Mesh:

Year:  2006        PMID: 16906550     DOI: 10.1002/ajmg.a.31421

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  13 in total

1.  First-trimester euploid miscarriages analysed by array-CGH.

Authors:  Chiara Donatella Viaggi; S Cavani; M Malacarne; F Floriddia; G Zerega; C Baldo; M Mogni; M Castagnetta; G Piombo; D A Coviello; F Camandona; D Lijoi; W Insegno; M Traversa; M Pierluigi
Journal:  J Appl Genet       Date:  2013-06-19       Impact factor: 3.240

2.  Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases.

Authors:  Larysa Y Pylyp; Lyudmyla O Spynenko; Nataliya V Verhoglyad; Anna O Mishenko; Dmytro O Mykytenko; Valery D Zukin
Journal:  J Assist Reprod Genet       Date:  2017-10-30       Impact factor: 3.412

3.  Genomic characteristics of miscarriage copy number variants.

Authors:  Hani Bagheri; Eloi Mercier; Ying Qiao; Mary D Stephenson; Evica Rajcan-Separovic
Journal:  Mol Hum Reprod       Date:  2015-06-12       Impact factor: 4.025

4.  Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.

Authors:  Trilochan Sahoo; Natasa Dzidic; Michelle N Strecker; Sara Commander; Mary K Travis; Charles Doherty; R Weslie Tyson; Arturo E Mendoza; Mary Stephenson; Craig A Dise; Carlos W Benito; Mandolin S Ziadie; Karine Hovanes
Journal:  Genet Med       Date:  2016-06-23       Impact factor: 8.822

5.  Somatic genomic variations in early human prenatal development.

Authors:  Caroline Robberecht; Evelyne Vanneste; Anne Pexsters; Thomas D'Hooghe; Thierry Voet; Joris R Vermeesch
Journal:  Curr Genomics       Date:  2010-09       Impact factor: 2.236

6.  Incidence of the 22q11.2 deletion in a large cohort of miscarriage samples.

Authors:  Melissa K Maisenbacher; Katrina Merrion; Barbara Pettersen; Michael Young; Kiyoung Paik; Sushma Iyengar; Stephanie Kareht; Styrmir Sigurjonsson; Zachary P Demko; Kimberly A Martin
Journal:  Mol Cytogenet       Date:  2017-03-09       Impact factor: 2.009

7.  Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion.

Authors:  Jinsong Gao; Congcong Liu; Fengxia Yao; Na Hao; Jing Zhou; Qian Zhou; Liang Zhang; Xinyan Liu; Xuming Bian; Juntao Liu
Journal:  Mol Cytogenet       Date:  2012-07-16       Impact factor: 2.009

8.  Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue.

Authors:  Rashmi Kudesia; Marilyn Li; Janice Smith; Ankita Patel; Zev Williams
Journal:  Reprod Biol Endocrinol       Date:  2014-03-03       Impact factor: 5.211

9.  Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory.

Authors:  Boris T Wang; Thomas P Chong; Fatih Z Boyar; Kimberly A Kopita; Leslie P Ross; Mohamed M El-Naggar; Trilochan Sahoo; Jia-Chi Wang; Morteza Hemmat; Mary H Haddadin; Renius Owen; Arturo L Anguiano
Journal:  Mol Cytogenet       Date:  2014-05-22       Impact factor: 2.009

10.  Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy.

Authors:  Stefanie Bug; Beate Solfrank; Felizitas Schmitz; Jana Pricelius; Mona Stecher; Andrew Craig; Marc Botcherby; Claudia Nevinny-Stickel-Hinzpeter
Journal:  Mol Cytogenet       Date:  2014-06-24       Impact factor: 2.009

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