Similar articles

• Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.

  Biselli JM, Machado FB, Zampieri BL, Alves da Silva AF, Goloni-Bertollo EM, Haddad R, Eberlin MN, Vannucchi H, Carvalho VM, Medina-Acosta E, Pavarino-Bertelli EC. Biselli JM, et al. Genet Couns. 2009;20(3):225-34. Genet Couns. 2009. PMID: 19852428
• Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes.

  Robinson A, Lubs HA, Nielsen J, Sørensen K. Robinson A, et al. Birth Defects Orig Artic Ser. 1979;15(1):261-6. Birth Defects Orig Artic Ser. 1979. PMID: 444644 No abstract available.
• The parental origin of the missing or additional chromosome in 45,X and 47,XXX females.

  Hassold T, Arnovitz K, Jacobs PA, May K, Robinson D. Hassold T, et al. Birth Defects Orig Artic Ser. 1990;26(4):297-304. Birth Defects Orig Artic Ser. 1990. PMID: 1982521
• [Chromosomal factors in sterility in men].

  Ganev V. Ganev V. Akush Ginekol (Sofiia). 1984;23(1):88-93. Akush Ginekol (Sofiia). 1984. PMID: 6372537 Review. Bulgarian. No abstract available.
• To err (meiotically) is human: the genesis of human aneuploidy.

  Hassold T, Hunt P. Hassold T, et al. Nat Rev Genet. 2001 Apr;2(4):280-91. doi: 10.1038/35066065. Nat Rev Genet. 2001. PMID: 11283700 Review.