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Page 1
Intellectual disability is associated with increased runs of homozygosity in simplex autism.
Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M; Simons Simplex Collection Genetics Consortium; Triche EW, Geschwind DH, State MW, Istrail S, Cook EH Jr, Devlin B, Morrow EM. Gamsiz ED, et al. Among authors: morrow em. Am J Hum Genet. 2013 Jul 11;93(1):103-9. doi: 10.1016/j.ajhg.2013.06.004. Epub 2013 Jul 3. Am J Hum Genet. 2013. PMID: 23830515 Free PMC article.
Ascertainment and gender in autism spectrum disorders.
Howe YJ, Yatchmink Y, Viscidi EW, Morrow EM. Howe YJ, et al. Among authors: morrow em. J Am Acad Child Adolesc Psychiatry. 2014 Jun;53(6):698-700. doi: 10.1016/j.jaac.2014.04.003. J Am Acad Child Adolesc Psychiatry. 2014. PMID: 24839890 Free PMC article. No abstract available.
Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome.
Pescosolido MF, Stein DM, Schmidt M, El Achkar CM, Sabbagh M, Rogg JM, Tantravahi U, McLean RL, Liu JS, Poduri A, Morrow EM. Pescosolido MF, et al. Among authors: morrow em. Ann Neurol. 2014 Oct;76(4):581-93. doi: 10.1002/ana.24225. Epub 2014 Sep 19. Ann Neurol. 2014. PMID: 25044251 Free PMC article.
Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein.
Pescosolido MF, Schwede M, Johnson Harrison A, Schmidt M, Gamsiz ED, Chen WS, Donahue JP, Shur N, Jerskey BA, Phornphutkul C, Morrow EM. Pescosolido MF, et al. Among authors: morrow em. J Med Genet. 2014 Sep;51(9):587-9. doi: 10.1136/jmedgenet-2014-102444. Epub 2014 Jul 23. J Med Genet. 2014. PMID: 25057125 Free PMC article. No abstract available.
125 results