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Infertility in a man with oligoasthenozoospermia associated with mosaic chromosome 22q11 deletion
BACKGROUND: A 30‐year‐old oligoasthenozoospermia man was found to have unbalance mosaic translocation between chromosome 22 and four other chromosomes (5, 6, 13, and 15) during the investigations for a couple with infertility for 3 years, which is a rare event in human pathology. METHODS: Classical...
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| Vydáno v: | Mol Genet Genomic Med |
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| Hlavní autoři: | , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6305647/ https://ncbi.nlm.nih.gov/pubmed/30461224 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.487 |
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