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Expanding the neurodevelopmental phenotype of PURA syndrome.
Lee BH, Reijnders MRF, Abubakare O, Tuttle E, Lape B, Minks KQ, Stodgell C, Bennetto L, Kwon J, Fong CT, Gripp KW, Marsh ED, Smith WE, Huq AM, Coury SA, Tan WH, Solis O, Mehta RI, Leventer RJ, Baralle D, Hunt D, Paciorkowski AR. Lee BH, et al. Among authors: bennetto l. Am J Med Genet A. 2018 Jan;176(1):56-67. doi: 10.1002/ajmg.a.38521. Epub 2017 Nov 17. Am J Med Genet A. 2018. PMID: 29150892 Free PMC article.
Molecular/clinical correlations in females with fragile X.
Sobesky WE, Taylor AK, Pennington BF, Bennetto L, Porter D, Riddle J, Hagerman RJ. Sobesky WE, et al. Among authors: bennetto l. Am J Med Genet. 1996 Aug 9;64(2):340-5. doi: 10.1002/(SICI)1096-8628(19960809)64:2<340::AID-AJMG21>3.0.CO;2-E. Am J Med Genet. 1996. PMID: 8844077
49 results