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Fragile X syndrome detection in newborns-pilot study.
Saul RA, Friez M, Eaves K, Stapleton GA, Collins JS, Schwartz CE, Stevenson RE. Saul RA, et al. Among authors: collins js. Genet Med. 2008 Oct;10(10):714-9. doi: 10.1097/GIM.0b013e3181862a76. Genet Med. 2008. PMID: 18813135 Free article.
Prevalence of aneuploidies in South Carolina in the 1990s.
Collins JS, Olson RL, DuPont BR, Wolff DJ, Best RG, Stevenson RE. Collins JS, et al. Genet Med. 2002 May-Jun;4(3):131-5. doi: 10.1097/00125817-200205000-00006. Genet Med. 2002. PMID: 12180147 Free article.
Genetic syndromes among individuals with mental retardation.
Stevenson RE, Procopio-Allen AM, Schroer RJ, Collins JS. Stevenson RE, et al. Among authors: collins js. Am J Med Genet A. 2003 Nov 15;123A(1):29-32. doi: 10.1002/ajmg.a.20492. Am J Med Genet A. 2003. PMID: 14556243
Cognitive function in Coffin-Lowry syndrome.
Simensen RJ, Abidi F, Collins JS, Schwartz CE, Stevenson RE. Simensen RJ, et al. Among authors: collins js. Clin Genet. 2002 Apr;61(4):299-304. doi: 10.1034/j.1399-0004.2002.610410.x. Clin Genet. 2002. PMID: 12030896
Neural tube defects and associated anomalies in South Carolina.
Stevenson RE, Seaver LH, Collins JS, Dean JH. Stevenson RE, et al. Among authors: collins js. Birth Defects Res A Clin Mol Teratol. 2004 Sep;70(9):554-8. doi: 10.1002/bdra.20062. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15368552
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
Boccuto L, Lauri M, Sarasua SM, Skinner CD, Buccella D, Dwivedi A, Orteschi D, Collins JS, Zollino M, Visconti P, Dupont B, Tiziano D, Schroer RJ, Neri G, Stevenson RE, Gurrieri F, Schwartz CE. Boccuto L, et al. Among authors: collins js. Eur J Hum Genet. 2013 Mar;21(3):310-6. doi: 10.1038/ejhg.2012.175. Epub 2012 Aug 15. Eur J Hum Genet. 2013. PMID: 22892527 Free PMC article.
147 results