Del Porto G - Search Results

1

20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome.

Grammatico P, Cupilari F, Di Rosa C, Falcolini M, Del Porto G. Grammatico P, et al. Among authors: del porto g. Clin Genet. 1992 Jun;41(6):285-9. doi: 10.1111/j.1399-0004.1992.tb03398.x. Clin Genet. 1992. PMID: 1623622

2

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: del porto g. Clin Genet. 1994 Sep;46(3):233-7. doi: 10.1111/j.1399-0004.1994.tb04232.x. Clin Genet. 1994. PMID: 7820937 Review.

3

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: del porto g. Genet Couns. 1997;8(1):39-42. Genet Couns. 1997. PMID: 9101277 Review.

4

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: del porto g. Genet Couns. 1997;8(4):327-34. Genet Couns. 1997. PMID: 9457503

5

A balanced complex chromosomal rearrangement (BCCR) with phenotypic effect.

Del Porto G, Grammatico P, De Sanctis S, Esposito M, Di Rosa C, Romano C. Del Porto G, et al. Clin Genet. 1991 Jul;40(1):57-61. doi: 10.1111/j.1399-0004.1991.tb03068.x. Clin Genet. 1991. PMID: 1884518

6

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: del porto g. Ann Genet. 1994;37(1):30-2. Ann Genet. 1994. PMID: 8010711

7

Granulomatous slack skin: cytogenetic and molecular analyses.

Grammatico P, Balus L, Scarpa S, Varesco L, Di Rosa C, Grammatico B, Del Porto G. Grammatico P, et al. Among authors: del porto g. Cancer Genet Cytogenet. 1994 Feb;72(2):96-100. doi: 10.1016/0165-4608(94)90122-8. Cancer Genet Cytogenet. 1994. PMID: 8143283

8

Trisomy 20 in a papillary urothelial carcinoma of the ureter.

Grammatico P, Lombardo A, Governatori M, Mordenti C, Poscente M, Del Porto G. Grammatico P, et al. Among authors: del porto g. Cancer Genet Cytogenet. 1996 Sep;90(2):132-4. doi: 10.1016/s0165-4608(96)90071-0. Cancer Genet Cytogenet. 1996. PMID: 8830722

9

Detection of a 46,XX,der(3)t(3;4)(p25;p16.1) by using chromosome microdissection.

Grammatico P, Roccella M, De Bernardo C, Roccella F, Grammatico B, Rinaldi R, Del Porto G. Grammatico P, et al. Among authors: del porto g. Genet Couns. 1998;9(4):259-64. Genet Couns. 1998. PMID: 9894162

10

46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.

Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G. Grammatico P, et al. Among authors: del porto g. Genet Couns. 1999;10(4):351-8. Genet Couns. 1999. PMID: 10631922

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