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Page 1
The transformative potential of law for gender and cancer.
Lancet. 2023 Dec 2;402(10417):2051-2053. doi: 10.1016/S0140-6736(23)01737-3. Epub 2023 Sep 26.
Lancet. 2023.
PMID: 37774728
No abstract available.
Endophenotyping social cognition in the broader autism phenotype.
Pua EPK, Desai T, Green C, Trevis K, Brown N, Delatycki M, Scheffer I, Wilson S.
Pua EPK, et al. Among authors: desai t.
Autism Res. 2023 Nov 30. doi: 10.1002/aur.3057. Online ahead of print.
Autism Res. 2023.
PMID: 38037242
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Tracing Autism Traits in Large Multiplex Families to Identify Endophenotypes of the Broader Autism Phenotype.
Trevis KJ, Brown NJ, Green CC, Lockhart PJ, Desai T, Vick T, Anderson V, Pua EPK, Bahlo M, Delatycki MB, Scheffer IE, Wilson SJ.
Trevis KJ, et al. Among authors: desai t.
Int J Mol Sci. 2020 Oct 27;21(21):7965. doi: 10.3390/ijms21217965.
Int J Mol Sci. 2020.
PMID: 33120939
Free PMC article.
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Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.
Mulley JC, Scheffer IE, Desai T, Bayly MA, Grinton BE, Vears DF, Berkovic SF, Dibbens LM.
Mulley JC, et al. Among authors: desai t.
Epilepsia. 2011 Oct;52(10):e139-42. doi: 10.1111/j.1528-1167.2011.03188.x. Epub 2011 Jul 21.
Epilepsia. 2011.
PMID: 21777232
Free article.
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Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families.
Hynes K, Tarpey P, Dibbens LM, Bayly MA, Berkovic SF, Smith R, Raisi ZA, Turner SJ, Brown NJ, Desai TD, Haan E, Turner G, Christodoulou J, Leonard H, Gill D, Stratton MR, Gecz J, Scheffer IE.
Hynes K, et al. Among authors: desai td.
J Med Genet. 2010 Mar;47(3):211-6. doi: 10.1136/jmg.2009.068817. Epub 2009 Sep 14.
J Med Genet. 2010.
PMID: 19752159
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