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20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome.
Clin Genet. 1992 Jun;41(6):285-9. doi: 10.1111/j.1399-0004.1992.tb03398.x.
Clin Genet. 1992.
PMID: 1623622
Del(4)(pter-->q33:) case report and review of the literature.
Grammatico P, Spaccini L, Di Rosa C, Cupilari F, Del Porto G.
Grammatico P, et al. Among authors: cupilari f.
Genet Couns. 1997;8(1):39-42.
Genet Couns. 1997.
PMID: 9101277
Review.
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2q35qter duplication syndrome: phenotypic definition.
Grammatico P, Di Rosa C, Rinaldi R, Roccella M, Cupilari F, Sbezzi T, Del Porto G.
Grammatico P, et al. Among authors: cupilari f.
Genet Couns. 1997;8(4):327-34.
Genet Couns. 1997.
PMID: 9457503
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First case of deletion 14q11.2q13: clinical phenotype.
Grammatico P, de Sanctis S, di Rosa C, Cupilari F, del Porto G.
Grammatico P, et al. Among authors: cupilari f.
Ann Genet. 1994;37(1):30-2.
Ann Genet. 1994.
PMID: 8010711
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