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Genetic defects in human azoospermia

As with many other diseases, genetic testing in human azoospermia was initially restricted to karyotype analyses (leading to diagnostic chromosome rearrangement tests for Klinefelter and other syndromes). With the advent of molecular biology in the 1980s, genetic screening was broadened to analyses...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Basic Clin Androl
Egile Nagusiak: Ghieh, Farah, Mitchell, Valérie, Mandon-Pepin, Béatrice, Vialard, François
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2019
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6477738/
https://ncbi.nlm.nih.gov/pubmed/31024732
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12610-019-0086-6
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