The following featured articles include those from NICHD researchers or NICHD-supported researchers.
- Hunter, J. E., Rohr, J. K., & Sherman, S. L. (2010). Co-occurring diagnoses among FMR1 premutation allele carriers. Clinical Genetics, 77, 374-381. PMID: 20059484
- Willemsen, R., Levenga, J., & Oostra, B. A. (2011). CGG repeat in the FMR1 gene. Clinical Genetics, 80, 214-225. PMID: 21651511
PubMed Search Results
Use the link below to search the PubMed database of more than 20 million citations for scientific articles with the key phrase "Fragile X associated primary ovarian insufficiency"
PubMed search results for articles with key phrase "Fragile X-Associated Primary Ovarian Insufficiency and NICHD"
PubMed search results for all articles with key phrase "Fragile X-Associated Primary Ovarian Insufficiency"