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47,XYY syndrome: clinical phenotype and timing of ascertainment.
Bardsley MZ, Kowal K, Levy C, Gosek A, Ayari N, Tartaglia N, Lahlou N, Winder B, Grimes S, Ross JL. Bardsley MZ, et al. J Pediatr. 2013 Oct;163(4):1085-94. doi: 10.1016/j.jpeds.2013.05.037. Epub 2013 Jun 27. J Pediatr. 2013. PMID: 23810129 Free PMC article.
Auditory evoked response delays in children with 47,XYY syndrome.
Bloy L, Ku M, Edgar JC, Miller JS, Blaskey L, Ross J, Roberts TPL. Bloy L, et al. Among authors: ross j. Neuroreport. 2019 May 1;30(7):504-509. doi: 10.1097/WNR.0000000000001233. Neuroreport. 2019. PMID: 30896674 Free PMC article.
Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.
Tartaglia N, Howell S, Davis S, Kowal K, Tanda T, Brown M, Boada C, Alston A, Crawford L, Thompson T, van Rijn S, Wilson R, Janusz J, Ross J. Tartaglia N, et al. Among authors: ross j. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):428-443. doi: 10.1002/ajmg.c.31807. Epub 2020 Jun 7. Am J Med Genet C Semin Med Genet. 2020. PMID: 32506668 Free PMC article. Review.
9,007 results