Results 1 to 10 of about 112 (72)

Duplo y: ¿estigmatización genética?

Revista Cubana de Investigaciones Biomédicas, 1999
La estigmatización genética constituye un hecho que cobra fuerza con los avances de la biología molecular, y el descubrimiento de cada nuevo gen, que aportan las investigaciones del proyecto Genoma Humano, pero existen síndromes como el XYY, que desde su
Héctor I Pimentel Benítez, Jaime Fajardo Castellanos, Julia García Capote   +2 more
doaj  

Duplo y: ¿estigmatización genética?

Revista Cubana de Investigaciones Biomédicas
La estigmatización genética constituye un hecho que cobra fuerza con los avances de la biología molecular, y el descubrimiento de cada nuevo gen, que aportan las investigaciones del proyecto Genoma Humano, pero existen síndromes como el XYY, que desde su
Héctor I Pimentel Benítez, Jaime Fajardo Castellanos, Julia García Capote   +2 more
doaj  

Birth of mice from meiotically arrested spermatocytes following biparental meiosis in halved oocytes. [PDF]

EMBO Rep, 2022
Ogonuki N, Kyogoku H, Hino T, Osawa Y, Fujiwara Y, Inoue K, Kunieda T, Mizuno S, Tateno H, Sugiyama F, Kitajima TS, Ogura A.   +11 more
europepmc   +1 more source

A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma-Systematic Review of the Literature, Meta-Analysis and Case Series. [PDF]

Diagnostics (Basel), 2022
Mastromoro G, Guadagnolo D, Khaleghi Hashemian N, Bernardini L, Giancotti A, Piacentini G, De Luca A, Pizzuti A.   +7 more
europepmc   +1 more source

Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study. [PDF]

Turk J Urol, 2020
Özdemir TR, Özyılmaz B, Çakmak Ö, Kaya ÖÖ, Köse C, Kırbıyık Ö, Keskin MZ, Koç A, Zeyrek T, Kutbay YB, Erdoğan KM, Güvenç MS.   +11 more
europepmc   +1 more source

Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women. [PDF]

Iran J Public Health, 2019
Li H, Li Y, Zhao R, Zhang Y.
europepmc   +1 more source

Double Aneuploidy 48,XXY,+21 Associated with a Congenital Heart Defect in a Neonate. [PDF]

Balkan J Med Genet, 2013
Shu X, Zou C, Shen Z.
europepmc   +1 more source

Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road? [PDF]

Clin Chem, 2014
Bianchi DW, Wilkins-Haug L.
europepmc   +1 more source

Sex-ratio meiotic drive in Drosophila simulans is related to equational nondisjunction of the Y chromosome. [PDF]

Genetics, 2000
Cazemajor M, Joly D, Montchamp-Moreau C.
europepmc   +1 more source

Abnormal children of a 47,XYY father. [PDF]

J Med Genet, 1979
Stoll C, Flori E, Clavert A, Beshara D, Buck P.   +4 more
europepmc   +1 more source