ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] We previously identified 75 Finnish females with hypergonadotropic ovarian dysgenesis (ODG), and later found that 22 of these females had an inactivating point mutation in the FSHR gene1,6. These patients came from 13 families and had 25 male sibs. In the present study, we obtained blood samples ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng0297-205
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