Results 71 to 80 of about 3,112 (176)

TRIPLOID KARYOTYPES IN PRENATAL DIAGNOSIS AT UNIVERSITY CLINICAL CENTER OF REPUBLIC OF SRPSKA

Genetics & Applications, 2017
Triploidy is chromosomal abnormality characterized by the presence of three sets of chromosomes instead of the normal two sets, so the triploid fetus has 69 chromosomes.
Marija Vuković, Zoran Obradović, Radmila Malešević, Željko Karan, Dženita Kurtćehajić, Svjetlana Uletilović, Branka Samardžić, Tijana Jaroš   +7 more
doaj  

Identification of chromosomal abnormalities and genomic features in near-triploidy/tetraploidy-acute leukemia by fluorescence in situ hybridization

Cancer Management and Research, 2019
Ruqing Yang,1 Minghua Jiang,2 Junzhao Zhao,1 Hui Chen,2 Jian Gong,2 Yaying You,3 Laiyue Song,3 Zhen Li,4 Qian Li2 1Reproductive Medicine Center, Department of Gynaecology and Obstetrics, The Second Affiliated Hospital and Yuying Children’s Hospital
Yang R, Jiang M, Zhao J, Chen H, Gong J, You Y, Song L, Li Z, Li Q   +8 more
doaj  

Origin and development of uniparental and polyploid blastomeres

iScience
Summary: Whole-genome (WG) abnormalities, such as uniparental diploidy and triploidy, cause fetal death. Occasionally, they coexist with biparental diploid cells in live births. Understanding the origin and early development of WG abnormal blastomeres is
Yan Zhao, Andrea Fernández-Montoro, Greet Peeters, Tatjana Jatsenko, Tine De Coster, Daniel Angel-Velez, Thomas Lefevre, Thierry Voet, Olga Tšuiko, Ants Kurg, Katrien Smits, Ann Van Soom, Joris Robert Vermeesch   +12 more
doaj   +1 more source

triploidy

Citation: 'triploidy' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.11320 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Underrecognized triploidy and genome-wide uniparental disomy in human blastocysts revealed by a concurrent preimplantation genetic testing approach. [PDF]

Hum Reprod Open
Li Y, Chau MHK, Zhang YX, Gui BH, Lui WT, Lam CMV, Cao Y, Chung TCY, Wu CC, Ip PNP, Chan DYL, Kwok YKY, Chung JPW, Choy KW.   +13 more
europepmc   +1 more source

The value of quantitative fluorescence polymerase chain reaction for the products of conception in the era of copy number variation sequencing. [PDF]

Front Genet
Yang S, Zhang H, Wang Y, Zhang Q, Wu Y, Fu X, Li R.   +6 more
europepmc   +1 more source

Whole-genome paternal uniparental disomy identified through prenatal single-nucleotide polymorphism-based cell-free DNA screening. [PDF]

Ultrasound Obstet Gynecol
Benn P, Hashimoto K, Souter V, Dhamankar R, Xu W, Kijacic D.   +5 more
europepmc   +1 more source

Placental mosaicism in prenatal diagnosis. [PDF]

Med Genet
Döttelmayer P, Fauth C.
europepmc   +1 more source

Stage-Specific Transcriptomic Analysis Reveals Molecular Basis of Ovarian Sterility in Triploid Turbot (<i>Scophthalmus maximus</i>). [PDF]

Animals (Basel)
Sun X, Li L, Cheng L, Meng Z, Xu W, Liu X.   +5 more
europepmc   +1 more source

New insight about early miscarriage: a prenatal data-based study. [PDF]

J Transl Med
Zhu Y, Liu Y, Ren C, Liu J, Yang Q, Li N, Wang T, Zhang P, Xue J, Ren C, Liu L.   +10 more
europepmc   +1 more source