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9. A case of 48,XXY,21+ in an infant with Down's syndrome. Neu RL; Scheuer AQ; Gardner LI J Med Genet; 1971 Dec; 8(4):533-5. PubMed ID: 4260531 [No Abstract] [Full Text] [Related]
10. Double Trisomy 48,XXY,+21 in a Neonate with Congenital Heart Disease. Bijanzadeh M; Rajaei Behbahani S Arch Iran Med; 2020 May; 23(5):356-358. PubMed ID: 32383621 [TBL] [Abstract][Full Text] [Related]
11. A male case with double aneuploidy (48,XXY,+21). Akbas E; Soylemez F; Savasoglu K; Halliogluand O; Balci S Genet Couns; 2008; 19(1):59-63. PubMed ID: 18564502 [TBL] [Abstract][Full Text] [Related]
12. 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 Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428 [TBL] [Abstract][Full Text] [Related]
13. [Cytogenetic studies in children with Down's syndrome and in their relatives]. Ostojska J Pediatr Pol; 1972 Oct; 47(10):1231-8. PubMed ID: 4263834 [No Abstract] [Full Text] [Related]
14. On the peripheral location of the Y chromosome. Kowalski CJ; Nasjleti CE; Schmitt B Hum Genet; 1978 Oct; 44(2):123-35. PubMed ID: 153323 [TBL] [Abstract][Full Text] [Related]
15. Down's syndrome. Incidence of translocations in Finland. Hongell K; Gripenberg U; Iivanainen M Hum Hered; 1972; 22(1):7-14. PubMed ID: 4260911 [No Abstract] [Full Text] [Related]
16. Segmental Duplication QF-PCR: A Simple and Alternative Method of Rapid Aneuploidy Testing for Developing Country Like India. Muthuswamy S; Agarwal S J Clin Lab Anal; 2017 Mar; 31(2):. PubMed ID: 27580119 [TBL] [Abstract][Full Text] [Related]
17. Down-Klinefelter syndrome (48,XXY,+21) in a neonate associated with congenital heart disease. Rodrigues MA; Morgade LF; Dias LFA; Moreira RV; Maia PD; Sales AFH; Ribeiro PD Genet Mol Res; 2017 Sep; 16(3):. PubMed ID: 28973759 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of double aneuploidy, 48,XXY,+21, and review of the literature. Jeanty C; Turner C J Ultrasound Med; 2009 May; 28(5):673-81. PubMed ID: 19389908 [No Abstract] [Full Text] [Related]
19. [Some genetic determinants and phenotype features in Klinefelter's syndrome at puberty]. KrawczyĆski M Wiad Lek; 1974 Oct; 27(20):1783-91. PubMed ID: 4432493 [No Abstract] [Full Text] [Related]
20. XXY son of XX-XXX mother. Geisler M; Svejcar J; Degenhardt KH Lancet; 1972 Apr; 1(7757):955. PubMed ID: 4112113 [No Abstract] [Full Text] [Related] [Next] [New Search]