Romano C - 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: romano c. 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: romano c. 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

Phenotypic and phoniatric findings in mosaic cri du chat syndrome.

Romano C, Ragusa RM, Scillato F, Greco D, Amato G, Barletta C. Romano C, et al. Am J Med Genet. 1991 Jun 15;39(4):391-5. doi: 10.1002/ajmg.1320390405. Am J Med Genet. 1991. PMID: 1877615 Review.

4

Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi syndrome.

Calì F, Failla P, Chiavetta V, Ragalmuto A, Ruggeri G, Schinocca P, Schepis C, Romano V, Romano C. Calì F, et al. Among authors: romano c, romano v. Genet Mol Res. 2013 Jan 7;12(3):2809-15. doi: 10.4238/2013.January.7.2. Genet Mol Res. 2013. PMID: 23315884 Free article.

5

A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.

Milone G, Conti L, Rizzo R, Sanfilippo S, Sammito V, Romano C. Milone G, et al. Among authors: romano c. Am J Med Genet. 1988 May-Jun;30(1-2):177-83. doi: 10.1002/ajmg.1320300116. Am J Med Genet. 1988. PMID: 3177443

6

A new MRXS locus maps to the X chromosome pericentromeric region: a new syndrome or narrow definition of Sutherland-Haan genetic locus?

Fichera M, Borgione E, Avola E, Amata S, Sturnio M, Romano C, Ragusa A. Fichera M, et al. Among authors: romano c. J Med Genet. 2002 Apr;39(4):276-80. doi: 10.1136/jmg.39.4.276. J Med Genet. 2002. PMID: 11950858 Free PMC article. No abstract available.

7

Growth hormone subnormality in Down syndrome.

Ragusa L, Romano C, Failla P, Proto C, Colabucci F. Ragusa L, et al. Among authors: romano c. Am J Med Genet. 1992 Jul 15;43(5):894-5. doi: 10.1002/ajmg.1320430529. Am J Med Genet. 1992. PMID: 1386497 No abstract available.

8

Seizures in patients with trisomy 21.

Romano C, Tiné A, Fazio G, Rizzo R, Colognola RM, Sorge G, Bergonzi P, Pavone L. Romano C, et al. Am J Med Genet Suppl. 1990;7:298-300. doi: 10.1002/ajmg.1320370758. Am J Med Genet Suppl. 1990. PMID: 2149964

9

Facial midline defect in the fetal alcohol syndrome: embryogenetic considerations in two clinical cases.

Neri G, Sammito V, Romano C, Sanfilippo S, Opitz JM. Neri G, et al. Among authors: romano c. Am J Med Genet. 1988 Mar;29(3):477-82. doi: 10.1002/ajmg.1320290302. Am J Med Genet. 1988. PMID: 3376992

10

Ichthyosis and neutral lipid storage disease.

Musumeci S, D'Agata A, Romano C, Patané R, Cutrona D. Musumeci S, et al. Among authors: romano c. Am J Med Genet. 1988 Feb;29(2):377-82. doi: 10.1002/ajmg.1320290219. Am J Med Genet. 1988. PMID: 3354610

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