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Neurological and endocrine phenotypes of fragile X carrier women.
Hall D, Todorova-Koteva K, Pandya S, Bernard B, Ouyang B, Walsh M, Pounardjian T, Deburghraeve C, Zhou L, Losh M, Leehey M, Berry-Kravis E. Hall D, et al. Among authors: losh m. Clin Genet. 2016 Jan;89(1):60-7. doi: 10.1111/cge.12646. Epub 2015 Sep 4. Clin Genet. 2016. PMID: 26212380 Free PMC article.
Associated features in females with an FMR1 premutation.
Wheeler AC, Bailey DB Jr, Berry-Kravis E, Greenberg J, Losh M, Mailick M, Milà M, Olichney JM, Rodriguez-Revenga L, Sherman S, Smith L, Summers S, Yang JC, Hagerman R. Wheeler AC, et al. Among authors: losh m. J Neurodev Disord. 2014;6(1):30. doi: 10.1186/1866-1955-6-30. Epub 2014 Jul 30. J Neurodev Disord. 2014. PMID: 25097672 Free PMC article. Review.
Common-variant associations with fragile X syndrome.
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Crowley JJ, et al. Among authors: losh m. Mol Psychiatry. 2019 Mar;24(3):338-344. doi: 10.1038/s41380-018-0290-3. Epub 2018 Dec 7. Mol Psychiatry. 2019. PMID: 30531935 Free PMC article.
72 results