Mollica F - Search Results

1

RFLP analysis in 5 Sicilian families with the fragile X syndrome.

Romano V, Mascali G, Chiavetta V, Ragusa RM, Barletta C, Romano C, Mollica F, Mattina T, Gross A, Brown WT, et al. Romano V, et al. Among authors: mollica f. Am J Med Genet. 1991 Feb-Mar;38(2-3):347-8. doi: 10.1002/ajmg.1320380236. Am J Med Genet. 1991. PMID: 1673309 No abstract available.

2

The fragile X in Sicily: an epidemiological survey.

Neri G, Sanfilippo S, Pavone L, Mollica F, Barberi I, Giuffrè L, Romano C, Mattina T, Cammarata M, Ragusa MG, et al. Neri G, et al. Among authors: mollica f. Am J Med Genet. 1988 May-Jun;30(1-2):665-72. doi: 10.1002/ajmg.1320300167. Am J Med Genet. 1988. PMID: 3177477

3

Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.

Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G. Gangarossa S, et al. Among authors: mollica f. Am J Med Genet. 1996 Mar 15;62(2):120-3. doi: 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8882392

4

Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.

Mattina T, Pierluigi M, Mazzone D, Scardilli S, Perfumo C, Mollica F. Mattina T, et al. Among authors: mollica f. J Med Genet. 1997 Nov;34(11):945-8. doi: 10.1136/jmg.34.11.945. J Med Genet. 1997. PMID: 9391894 Free PMC article.

5

Antley-Bixler syndrome.

Mattina T, Pierluigi M, Perfumo C, Mazzone D, Scardilli S, Mollica F. Mattina T, et al. Among authors: mollica f. Clin Genet. 1996 Oct;50(4):277. doi: 10.1111/j.1399-0004.1996.tb02646.x. Clin Genet. 1996. PMID: 9001819 No abstract available.

6

Wolfram's syndrome and HLA.

Mattina T, Li Volti S, Palmeri P, Tribulato A, Salerno A, Mollica F. Mattina T, et al. Among authors: mollica f. Ophthalmic Paediatr Genet. 1988 Mar;9(1):25-8. doi: 10.3109/13816818809031477. Ophthalmic Paediatr Genet. 1988. PMID: 3043304 Review.

7

Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe.

Guldberg P, Romano V, Ceratto N, Bosco P, Ciuna M, Indelicato A, Mollica F, Meli C, Giovannini M, Riva E, et al. Guldberg P, et al. Among authors: mollica f. Hum Mol Genet. 1993 Oct;2(10):1703-7. doi: 10.1093/hmg/2.10.1703. Hum Mol Genet. 1993. PMID: 8268925

8

Maternal transmission of HBV infection.

Mollica F, Musumeci S, Mattina T, Rugolo S. Mollica F, et al. Pediatrics. 1980 Feb;65(2):369. Pediatrics. 1980. PMID: 7354994 No abstract available.

9

Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities.

Dunnill MG, Richards AJ, Milana G, Mollica F, Atherton D, Winship I, Farrall M, al-Imara L, Eady RA, Pope FM. Dunnill MG, et al. Among authors: mollica f. J Med Genet. 1994 Oct;31(10):745-8. doi: 10.1136/jmg.31.10.745. J Med Genet. 1994. PMID: 7837248 Free PMC article.

10

Twins with acardia and anencephaly.

Pavone L, Laurence KM, Mattina T, Nuciforo G, Mollica F. Pavone L, et al. Among authors: mollica f. Acta Genet Med Gemellol (Roma). 1985;34(1-2):89-93. doi: 10.1017/s0001566000004967. Acta Genet Med Gemellol (Roma). 1985. PMID: 4050300

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