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Congenital heart disease in the 48,XXYY syndrome.
Meschede D, Nekarda T, Kececioglu D, Löser H, Vogt J, Miny P, Horst J. Meschede D, et al. Clin Genet. 1995 Aug;48(2):100-2. doi: 10.1111/j.1399-0004.1995.tb04064.x. Clin Genet. 1995. PMID: 7586648
Isochromosome Xq in Klinefelter syndrome: report of 7 new cases.
Arps S, Koske-Westphal T, Meinecke P, Meschede D, Nieschlag E, Harprecht W, Steuber E, Back E, Wolff G, Kerber S, Held KR. Arps S, et al. Among authors: meschede d. Am J Med Genet. 1996 Sep 6;64(4):580-2. doi: 10.1002/(SICI)1096-8628(19960906)64:4<580::AID-AJMG10>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870925
93 results