Results 161 to 170 of about 89,619 (298)
ABSTRACT Fetal congenital anomalies and genetic disorders complicate 3%–5% of pregnancies and can have a significant impact on pregnancy outcomes. Precise and individualized prenatal diagnosis is crucial for effective counseling and management.
Sarah Araji +4 more
wiley +1 more source
Characteristics and prognosis of paediatric normal karyotype acute myeloid leukaemia: A NOPHO-DBH AML study. [PDF]
Herlin MK +18 more
europepmc +1 more source
Karyotype of <i>Presbytis entellus entellus</i> (Primate)
T. Sharma, Surabhi Kakati
openalex +2 more sources
A patient with 45,X-46,XXq--46,XXq-dic karyotype. [PDF]
A. C. Stevenson +2 more
openalex +1 more source
ABSTRACT Objective To evaluate the diagnostic value of prenatal exome sequencing (ES) integrated with copy number variant (CNV) and single nucleotide variant (SNV) analysis (ES‐CNV/SNV) in fetuses with structural anomalies following negative chromosomal microarray analysis (CMA) and karyotyping, and to delineate the practical challenges encountered ...
Yulin Jiang +21 more
wiley +1 more source
Chromosomal Inversion Associated With Diet Differences in Common Quails Sharing Wintering Grounds. [PDF]
Vinagre-Izquierdo C +4 more
europepmc +1 more source
Identification of the Mouse Karyotype by Quinacrine Fluorescence, and Tentative Assignment of Seven Linkage Groups [PDF]
O. J. Miller +6 more
openalex +1 more source
ABSTRACT Objective To evaluate the performance of non‐invasive prenatal testing (NIPT) in vanishing‐twin and multiple pregnancies. Methods This study was conducted as part of the TRIDENT‐2 study, in which NIPT was offered as a first‐tier screening test to women with a multiple pregnancy or vanishing‐twin pregnancy between 1 June 2020 and 31 March 2023 ...
J. C. A. van Eekhout +86 more
wiley +1 more source

