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The phenotype of a 45,X male with a Y/18 translocation.
Clin Genet. 1996 Jan;49(1):37-41. doi: 10.1111/j.1399-0004.1996.tb04322.x.
Clin Genet. 1996.
PMID: 8721570
ICF syndrome with variable expression in sibs.
Gimelli G, Varone P, Pezzolo A, Lerone M, Pistoia V.
Gimelli G, et al. Among authors: varone p.
J Med Genet. 1993 May;30(5):429-32. doi: 10.1136/jmg.30.5.429.
J Med Genet. 1993.
PMID: 8320711
Free PMC article.
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Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.
Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C, Sujansky E, Dallapiccola B, Zuffardi O.
Giglio S, et al. Among authors: varone p.
Circulation. 2000 Jul 25;102(4):432-7. doi: 10.1161/01.cir.102.4.432.
Circulation. 2000.
PMID: 10908216
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