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Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
Primary hypogonadism combined with Müllerian hypoplasia and partial alopecia are common features of this syndrome, which was reported only in four earlier families from areas where consanguineous marriage is prevalent. An autosomal recessive pattern of inheritance was suggested earlier and is suppor...
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| Vydáno v: | Clin Case Rep |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5628201/ https://ncbi.nlm.nih.gov/pubmed/29026561 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1128 |
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