Romeo G - Search Results

1

Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene.

Covone AE, Lerone M, Romeo G. Covone AE, et al. Among authors: romeo g. Hum Genet. 1991 Jul;87(3):353-60. doi: 10.1007/BF00200919. Hum Genet. 1991. PMID: 1864612

2

Assignment of human aldolase C gene to chromosome 17, region cen----q21.1.

Rocchi M, Vitale E, Covone A, Romeo G, Santamaria R, Buono P, Paolella G, Salvatore F. Rocchi M, et al. Among authors: romeo g. Hum Genet. 1989 Jun;82(3):279-82. doi: 10.1007/BF00291170. Hum Genet. 1989. PMID: 2731939

3

Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection.

Puliti A, Covone AE, Bicocchi MP, Bolino A, Lerone M, Martucciello G, Jasonni V, Romeo G. Puliti A, et al. Among authors: romeo g. Cytogenet Cell Genet. 1993;63(2):102-6. doi: 10.1159/000133510. Cytogenet Cell Genet. 1993. PMID: 8467706

4

SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function.

Nigro V, Bruni P, Ciccodicola A, Politano L, Nigro G, Piluso G, Cappa V, Covone AE, Romeo G, D'Urso M. Nigro V, et al. Among authors: romeo g. Hum Mol Genet. 1995 Oct;4(10):2003-4. doi: 10.1093/hmg/4.10.2003. Hum Mol Genet. 1995. PMID: 8595433 No abstract available.

5

[Identification of the dystrophin gene deletions in DMD/BMD patients. Analysis of the reading frame shift and germinal mosaicism].

Covone AE, Caroli F, Cereseto A, Lerone M, Romeo G. Covone AE, et al. Among authors: romeo g. Minerva Pediatr. 1991 Mar;43(3):65-6. Minerva Pediatr. 1991. PMID: 1870527 Italian. No abstract available.

6

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Among authors: romeo g. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.

7

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

8

Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR.

Covone AE, Caroli F, Romeo G. Covone AE, et al. Among authors: romeo g. Am J Hum Genet. 1992 Sep;51(3):675-7. Am J Hum Genet. 1992. PMID: 1496997 Free PMC article. No abstract available.

9

The gene coding for proteins HC and HI-30 of inter-alpha-trypsin inhibitor maps to 9q22.3----q33.

Traboni C, Tosini F, Covone A, Romeo G, Rocchi M. Traboni C, et al. Among authors: romeo g. Cytogenet Cell Genet. 1989;50(1):46-8. doi: 10.1159/000132717. Cytogenet Cell Genet. 1989. PMID: 2472935

10

Regional mapping of RBP4 to 10q23----q24 and RBP1 to 3q21----q22 in man.

Rocchi M, Covone A, Romeo G, Faraonio R, Colantuoni V. Rocchi M, et al. Among authors: romeo g. Somat Cell Mol Genet. 1989 Mar;15(2):185-90. doi: 10.1007/BF01535081. Somat Cell Mol Genet. 1989. PMID: 2928844

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