Results 231 to 240 of about 317,190 (282)

Weighted Single‐Step GWAS Reveals Genetic Mechanisms Underlying Pregnancy Loss in Early Nellore Heifers

Animal Genetics, Volume 57, Issue 5, October 2026.
ABSTRACT Pregnancy loss (PL) affects reproductive efficiency in beef cattle, yet its genetic architecture remains poorly understood in Bos indicus populations. Here, PL was defined as failure from pregnancy diagnosis to calving, capturing a window approximately 60 days after the breeding season.
Flávia C. Bis, Nedenia Bonvino Stafuzza, Elisângela Chicaroni de Mattos, Angélica Simone Cravo Pereira, José Bento Sterman Ferraz, Fernando Baldi, Sabrina T. Amorim   +6 more
wiley   +1 more source

Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing. [PDF]

Sci Rep
Guo R, Duan C, Zarrei M, Reuter MS, Dong R, Zhang G, Yang X, Zhang H, Wang Y, Scherer SW, Liu Y, Gai Z.   +11 more
europepmc   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2331-2337, October 2026.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli, Giulia Bruna Marchetti, Maria Iascone, Maria Grazia Patricelli, Sara Giangiobbe, Gabriella Cinzia Pozzobon, Miriam Nella Savini, Fabio Giglio, Alessandro Aiuti, Paola Carrera, Francesca Ferrua, Angela Peron   +11 more
wiley   +1 more source

Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft Markers. [PDF]

J Clin Lab Anal
Liu L, She L, Zheng Z, Huang S, Wu H.
europepmc   +1 more source

Increased nuchal translucency thickness and normal chromosomal microarray: Danish nationwide cohort study. [PDF]

Ultrasound Obstet Gynecol
Gadsbøll K, Brix N, Sandager P, Petersen OB, Souka AP, Nicolaides KH, Vogel I.   +6 more
europepmc   +1 more source

The assessing of clinical relevance of chromosomal microarray analysis in the prenatal diagnosis of fetal growth restriction. [PDF]

BMC Pregnancy Childbirth
Li P, Wu W, Zhang X, Li Y, Liu M, Wang Y, Man D, Wang F.   +7 more
europepmc   +1 more source

Phase Determination and Demonstration of Parental Mosaicism of Intragenic <i>PRKN</i> Deletions Initially Identified by Chromosomal Microarray Analysis. [PDF]

Genes (Basel)
Choate LA, Hoffman F, Newman JH, Runke C, Webley M, Hoppman NL, Thorland EC.   +6 more
europepmc   +1 more source

Genetic Alterations in Atypical Cerebral Palsy Identified Through Chromosomal Microarray and Exome Sequencing. [PDF]

Int J Mol Sci
Han JY, Gwack J, Kim JH, Park MK, Park J.   +4 more
europepmc   +1 more source

Application of Chromosomal Karyotype Analysis Combined With Chromosomal Microarray Analysis in the Amniotic Fluid of Advanced Maternal Age. [PDF]

J Clin Lab Anal
Liu C, Lu Y, Zhang B, Yu L, He J, Ji Y.
europepmc   +1 more source

Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study

American Journal of Obstetrics and Gynecology, 2021
International audienceBackground: Compared with standard karyotype, chromosomal microarray analysis improves the detection of genetic anomalies and is thus recommended in many prenatal indications.
Jérôme MASSARDIER, Alexandra Benachi, RECEVEUR Aline   +2 more
exaly   +2 more sources