Cargando…
Complex Y chromosome anomalies in an infertile male
Y chromosome anomalies are closely associated with non-obstructive azoospermia (NOA), a major etiology in male infertility. Klinefelter syndrome (KS) and Y chromosome microdeletions are some of the well-identified genetic defects in this regard, while Y chromosome aneuploidies have been reported to...
Autores principales: | Kaluarachchi, Nirmani P, Randunu, Malshani H, Jainulabdeen, Munshifa, Thavarajah, Arunthusha, Padeniya, Padmapani, Galhena, Prasanna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Brazilian Society of Assisted Reproduction
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7558904/ https://www.ncbi.nlm.nih.gov/pubmed/32490605 http://dx.doi.org/10.5935/1518-0557.20200022 |
Ejemplares similares
-
Frequency of Hereditary Hemochromatosis Gene (HFE) Variants in Sri Lankan Transfusion-Dependent Beta-Thalassemia Patients and Their Association With the Serum Ferritin Level
por: Padeniya, Padmapani, et al.
Publicado: (2022) -
AB26. Y chromosome and male infertility
por: Iijima, Masashi
Publicado: (2014) -
An evolutionary perspective on Y-chromosomal variation and male infertility
por: Tyler-Smith, Chris
Publicado: (2008) -
Screening of ‘Y’ chromosome microdeletions in Iranian infertile males
por: Malekasgar, Ali Mohammad, et al.
Publicado: (2008) -
The X chromosome and male infertility
por: Vockel, Matthias, et al.
Publicado: (2019)