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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
Inv dup(15): contribution to the clinical definition of phenotype.
Grammatico P, Di Rosa C, Roccella M, Falcolini M, Pelliccia A, Roccella F, Del Porto G.
Grammatico P, et al. Among authors: falcolini m.
Clin Genet. 1994 Sep;46(3):233-7. doi: 10.1111/j.1399-0004.1994.tb04232.x.
Clin Genet. 1994.
PMID: 7820937
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