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Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Soorya L, Kolevzon A, Zweifach J, Lim T, Dobry Y, Schwartz L, Frank Y, Wang AT, Cai G, Parkhomenko E, Halpern D, Grodberg D, Angarita B, Willner JP, Yang A, Canitano R, Chaplin W, Betancur C, Buxbaum JD. Soorya L, et al. Among authors: willner jp. Mol Autism. 2013 Jun 11;4(1):18. doi: 10.1186/2040-2392-4-18. Mol Autism. 2013. PMID: 23758760 Free PMC article.
Paternal uniparental disomy for chromosome 14: a case report and review.
Cotter PD, Kaffe S, McCurdy LD, Jhaveri M, Willner JP, Hirschhorn K. Cotter PD, et al. Among authors: willner jp. Am J Med Genet. 1997 May 2;70(1):74-9. doi: 10.1002/(sici)1096-8628(19970502)70:1<74::aid-ajmg14>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9129745 Review.
35 results