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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.
Testicular function in boys with 47,XYY and relationship to phenotype.
Davis SM, Bloy L, Roberts TPL, Kowal K, Alston A, Tahsin A, Truxon A, Ross JL. Davis SM, et al. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):371-385. doi: 10.1002/ajmg.c.31790. Epub 2020 Jun 16. Am J Med Genet C Semin Med Genet. 2020. PMID: 32544298 Free PMC article.
A new look at XXYY syndrome: medical and psychological features.
Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. Tartaglia N, et al. Among authors: ross j. Am J Med Genet A. 2008 Jun 15;146A(12):1509-22. doi: 10.1002/ajmg.a.32366. Am J Med Genet A. 2008. PMID: 18481271 Free PMC article.
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.
8,983 results