Results 31 to 40 of about 317,190 (282)

Prenatal diagnosis and genetic counseling of mosaicism for chromosome t (7; 14) with a favorable outcome

Clinical and Experimental Obstetrics & Gynecology, 2020
We report a case of prenatal diagnosis of mosaicism for chromosome t (7; 14) with a favorable fetal outcome. Similar chromosomal abnormalities have been observed in patients with hematologic malignancy.
D. Lu, D. Cao, Q. Zhao, X. Chen
doaj   +1 more source

Microarray sub-grid detection: A novel algorithm [PDF]

, 2007
This is the post print version of the article. The official published version can be obtained from the link below - Copyright 2007 Taylor & Francis LtdA novel algorithm for detecting microarray subgrids is proposed. The only input to the algorithm is the
Liu, X, Wang, Z, Morris, D
core   +1 more source

Regional regulation of transcription in the chicken genome [PDF]

, 2010
Background Over the past years, the relationship between gene transcription and chromosomal location has been studied in a number of different vertebrate genomes. Regional differences in gene expression have been found in several different species.
Bastiaansen John WM, Nie, H., Nie Haisheng, Crooijmans, R.P.M.A., Groenen, M.A.M., Groenen Martien AM, Bastiaansen, J.W.M., Crooijmans Richard PMA, Megens, H.J.W.C., Megens Hendrik-Jan   +9 more
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The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly

Taiwanese Journal of Obstetrics & Gynecology, 2019
Objective: To investigate the clinical value of chromosomal microarray analysis (CMA) in the prenatal diagnosis of genetic abnormalities in fetal isolated mild ventriculomegaly.
Hong-Lei Duan, Xiang-Yu Zhu, Yu-Jie Zhu, Xing Wu, Guang-Feng Zhao, Wan-Jun Wang, Jie Li   +6 more
doaj   +1 more source

Development and validation of a bovine macrophage specific cDNA microarray [PDF]

, 2006
Background The response of macrophages to danger signals is an important early stage in the immune response. Our understanding of this complex event has been furthered by microarray analysis, which allows the simultaneous investigation of the expression ...
Waddington David, Jensen Kirsty, Talbot, Richard, Edith Paxton, Talbot Richard, Elizabeth J Glass, Paxton Edith, Paxton, Edith, David Waddington, Kirsty Jensen, Jensen, Kirsty, Glass, Elizabeth, Waddington, David, Glass Elizabeth J, Richard Talbot   +14 more
core   +1 more source

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis [PDF]

New England Journal of Medicine, 2012
Chromosomal microarray analysis has emerged as a primary diagnostic tool for the evaluation of developmental delay and structural malformations in children. We aimed to evaluate the accuracy, efficacy, and incremental yield of chromosomal microarray analysis as compared with karyotyping for routine prenatal diagnosis.Samples from women undergoing ...
Ronald J, Wapner, Christa Lese, Martin, Brynn, Levy, Blake C, Ballif, Christine M, Eng, Julia M, Zachary, Melissa, Savage, Lawrence D, Platt, Daniel, Saltzman, William A, Grobman, Susan, Klugman, Thomas, Scholl, Joe Leigh, Simpson, Kimberly, McCall, Vimla S, Aggarwal, Brian, Bunke, Odelia, Nahum, Ankita, Patel, Allen N, Lamb, Elizabeth A, Thom, Arthur L, Beaudet, David H, Ledbetter, Lisa G, Shaffer, Laird, Jackson   +23 more
openaire   +2 more sources

Chromosomal variants accumulate in genomes of the spontaneous aborted fetuses revealed by chromosomal microarray analysis.

PLoS ONE, 2021
Spontaneous abortion is an impeding factor for the success rates of human assistant reproductive technology (ART). Causes of spontaneous abortion include not only the pregnant mothers' health conditions and lifestyle habits, but also the fetal ...
Sen Li, Lei-Ling Chen, Xing-Hua Wang, Hai-Jing Zhu, Xiao-Long Li, Xie Feng, Lei Guo, Xiang-Hong Ou, Jun-Yu Ma   +8 more
doaj   +2 more sources

A Clinical and Molecular Description of a Rare Case of Chromosomal Abnormality (Partial Trisomy 14q11.2-q21.1 and Partial Monosomy 21q11.2-q21.3)

Вопросы современной педиатрии, 2016
The article presents a detailed clinical and molecular and cytogenetic analysis of the unique case of a rare chromosomal abnormality (duplication of 14q11.2-q21.1 and deletion of 21q11.2-q21.3).
Grigory S. Vasilyev, Tatiana I. Meshcheryakova, Elena N. Lukash, Svetlana S. Zhylina, Ilya V. Kanivets, Alexander N. Petrin   +5 more
doaj   +1 more source

Facilitating functional annotation of chicken microarray data [PDF]

, 2009
Background Modeling results from chicken microarray studies is challenging for researchers due to little functional annotation associated with these arrays.
Burgess Shane C, Gresham, Cathy R, Gresham Cathy R, Kumar Ranjit, Burgess, Shane C, Shane C Burgess, Kumar, Ranjit, Buza Teresia J, Cathy R Gresham, McCarthy, Fiona M, Teresia J Buza, Fiona M McCarthy, Ranjit Kumar, McCarthy Fiona M, Buza, Teresia J   +14 more
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An uninformative NIPT as an early indicator of cri‐du‐chat due to a chromosomal 5;18 translocation—An atypical presentation of a rare cytogenetic phenomenon

Clinical Case Reports, 2023
Key Clinical Message We present a patient with cri‐du‐chat syndrome secondary to a rare cytogenetic mechanism. Our patient was the product of a dichorionic diamniotic twin pregnancy initially flagged with soft markers on ultrasound and uninformative ...
Devanshi Shukla, Matthew Dinunzio, Samantha Colaiacovo, Anahita Mohseni Meybodi, Maha Saleh   +4 more
doaj   +1 more source