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Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndrome.
J Med Genet. 2007 Oct;44(10):647-50. doi: 10.1136/jmg.2007.050963.
J Med Genet. 2007.
PMID: 17911656
Free PMC article.
Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions.
Concolino D, Iembo MA, Rossi E, Giglio S, Coppola G, Miraglia Del Giudice E, Strisciuglio P.
Concolino D, et al. Among authors: iembo ma.
J Med Genet. 2002 Mar;39(3):214-6. doi: 10.1136/jmg.39.3.214.
J Med Genet. 2002.
PMID: 11897828
Free PMC article.
No abstract available.
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Ring chromosome 10 (p15q26) in a patient with unipolar affective disorder, multiple minor anomalies, and mental retardation.
Concolino D, Iembo MA, Moricca MT, Strisciuglio P, Marotta R, Rossi E, Giglio S.
Concolino D, et al. Among authors: iembo ma.
Am J Med Genet A. 2003 Dec 1;123A(2):201-3. doi: 10.1002/ajmg.a.20299.
Am J Med Genet A. 2003.
PMID: 14598349
No abstract available.
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A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
Concolino D, Iembo MA, Moricca MT, Rapsomaniki M, Marotta R, Galesi O, Fichera M, Romano C, Strisciuglio P.
Concolino D, et al. Among authors: iembo ma.
Eur J Med Genet. 2012 Jan;55(1):67-70. doi: 10.1016/j.ejmg.2011.09.001. Epub 2011 Sep 25.
Eur J Med Genet. 2012.
PMID: 21971480
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