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Search for altered imprinting marks in Mayer–Rokitansky–Küster–Hauser patients
BACKGROUND: Mayer–Rokitansky–Küster–Hauser syndrome (MRKH) is the second most common cause of primary amenorrhea and characterized by absence of the uterus and the upper part of the vagina. The etiology of MRKH is mainly unknown but a contribution of genomic alterations is probable. A molecular dist...
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| Pubblicato in: | Mol Genet Genomic Med |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6305658/ https://ncbi.nlm.nih.gov/pubmed/30099855 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.426 |
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