Romeo G - Search Results

1

Prevalence of mental retardation related to fragile X syndrome and other chromosomal abnormalities in the Republic of San Marino.

Cammarata S, Archidiacono N, Romeo G, Benassi G, Guarino M, D'Alessandro R. Cammarata S, et al. Among authors: romeo g. Dev Med Child Neurol. 1988 Oct;30(5):646-9. doi: 10.1111/j.1469-8749.1988.tb04803.x. Dev Med Child Neurol. 1988. PMID: 2976382

2

Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations.

Romeo G, Archidiacono N, Ferlini A, Rocchi M. Romeo G, et al. Am J Med Genet Suppl. 1986;1:355-9. doi: 10.1002/ajmg.1320250536. Am J Med Genet Suppl. 1986. PMID: 3087196

3

Chromosomal assignment of human O6-methylguanine-DNA-methyltransferase gene by hamster-human somatic cell hybrids.

Zunino A, Arena G, Rossi O, Archidiacono N, Rocchi M, Romeo G, Abbondandolo A. Zunino A, et al. Among authors: romeo g. Mutagenesis. 1991 Sep;6(5):395-7. doi: 10.1093/mutage/6.5.395. Mutagenesis. 1991. PMID: 1795645

4

Rett syndrome and fragile site in Xp22.

Archidiacono N, Rett A, Rocchi M, Rolando S, Lugaresi E, Romeo G. Archidiacono N, et al. Among authors: romeo g. Lancet. 1985 Nov 30;2(8466):1242-3. doi: 10.1016/s0140-6736(85)90767-6. Lancet. 1985. PMID: 2866315 No abstract available.

5

Assignment of the gene for human tenascin to the region q32-q34 of chromosome 9.

Rocchi M, Archidiacono N, Romeo G, Saginati M, Zardi L. Rocchi M, et al. Among authors: romeo g. Hum Genet. 1991 Apr;86(6):621-3. doi: 10.1007/BF00201554. Hum Genet. 1991. PMID: 1709136

6

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Archidiacono N, Lerone M, Rocchi M, Anvret M, Ozcelik T, Francke U, Romeo G. Archidiacono N, et al. Among authors: romeo g. Hum Genet. 1991 Apr;86(6):604-6. doi: 10.1007/BF00201549. Hum Genet. 1991. PMID: 1673961

7

Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies.

Romeo G, Devoto M, Archidiacono N, Ferlini A, Roncuzzi L, Melis MA, Paderi E, Ferrari M, Tedeschi S, Galluzzi G, et al. Romeo G, et al. Eur J Pediatr. 1988 May;147(4):412-5. doi: 10.1007/BF00496422. Eur J Pediatr. 1988. PMID: 3165066

8

Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks.

Ceccherini I, Lituania M, Cordone MS, Perfumo F, Gusmano R, Callea F, Archidiacono N, Romeo G. Ceccherini I, et al. Among authors: romeo g. Prenat Diagn. 1989 Nov;9(11):751-8. doi: 10.1002/pd.1970091103. Prenat Diagn. 1989. PMID: 2575745

9

Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1-acid glycoprotein to chromosome 9.

Rocchi M, Roncuzzi L, Santamaria R, Archidiacono N, Dente L, Romeo G. Rocchi M, et al. Among authors: romeo g. Hum Genet. 1986 Sep;74(1):30-3. doi: 10.1007/BF00278781. Hum Genet. 1986. PMID: 3463531

10

Mapping of human hexokinase 1 gene to 10q11----qter.

Daniele A, Altruda F, Ferrone M, Silengo L, Romeo G, Archidiacono N, Rocchi M. Daniele A, et al. Among authors: romeo g. Hum Hered. 1992;42(2):107-10. doi: 10.1159/000154049. Hum Hered. 1992. PMID: 1572668

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