Romeo G - Search Results

1

Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets.

Bolino A, Devoto M, Enia G, Zoccali C, Weissenbach J, Romeo G. Bolino A, et al. Among authors: romeo g. Eur J Hum Genet. 1993;1(4):269-79. doi: 10.1159/000472424. Eur J Hum Genet. 1993. PMID: 7915957

2

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing.

Bolino A, Brancolini V, Bono F, Bruni A, Gambardella A, Romeo G, Quattrone A, Devoto M. Bolino A, et al. Among authors: romeo g. Hum Mol Genet. 1996 Jul;5(7):1051-4. doi: 10.1093/hmg/5.7.1051. Hum Mol Genet. 1996. PMID: 8817346

3

A new candidate region for the positional cloning of the XLP gene.

Bolino A, Yin L, Seri M, Cusano R, Cinti R, Coffey A, Brooksbank R, Howell G, Bentley D, Davis JR, Lanyi A, Huang D, Stark M, Creaven M, Bjørkhaug L, Heitzmann F, Lamartine J, Gaudi S, Sylla BS, Lenoir GM, Castagnola E, Giacchino R, Porta G, Franco B, Zollo M, Sumegi J, Romeo G. Bolino A, et al. Among authors: romeo g. Eur J Hum Genet. 1998 Sep-Oct;6(5):509-17. doi: 10.1038/sj.ejhg.5200249. Eur J Hum Genet. 1998. PMID: 9801876

4

A second genetic locus for autosomal dominant polycystic kidney disease.

Romeo G, Devoto M, Costa G, Roncuzzi L, Catizone L, Zucchelli P, Germino GG, Keith T, Weatherall DJ, Reeders ST. Romeo G, et al. Lancet. 1988 Jul 2;2(8601):8-11. doi: 10.1016/s0140-6736(88)92943-1. Lancet. 1988. PMID: 2898665

5

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

6

Homogeneity of cystic fibrosis in Italy.

Vitale E, Devoto M, Mastella G, Romeo G. Vitale E, et al. Among authors: romeo g. Am J Hum Genet. 1986 Dec;39(6):832-6. Am J Hum Genet. 1986. PMID: 3467589 Free PMC article.

7

Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat.

Ceccherini I, Zhang AL, Matera I, Yang G, Devoto M, Romeo G, Cass DT. Ceccherini I, et al. Among authors: romeo g. Hum Mol Genet. 1995 Nov;4(11):2089-96. doi: 10.1093/hmg/4.11.2089. Hum Mol Genet. 1995. PMID: 8589685

8

Exclusion of the SCN2B gene as candidate for CMT4B.

Bolino A, Seri M, Caroli F, Eubanks J, Srinivasan J, Mandich P, Schenone A, Quattrone A, Romeo G, Catterall WA, Devoto M. Bolino A, et al. Among authors: romeo g. Eur J Hum Genet. 1998 Nov-Dec;6(6):629-34. doi: 10.1038/sj.ejhg.5200220. Eur J Hum Genet. 1998. PMID: 9887383

9

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.

Seri M, Cusano R, Forabosco P, Cinti R, Caroli F, Picco P, Bini R, Morra VB, De Michele G, Lerone M, Silengo M, Pela I, Borrone C, Romeo G, Devoto M. Seri M, et al. Among authors: romeo g. Am J Hum Genet. 1999 Feb;64(2):586-93. doi: 10.1086/302241. Am J Hum Genet. 1999. PMID: 9973297 Free PMC article.

10

A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease.

Griseri P, Sancandi M, Patrone G, Bocciardi R, Hofstra R, Ravazzolo R, Devoto M, Romeo G, Ceccherini I. Griseri P, et al. Among authors: romeo g. Eur J Hum Genet. 2000 Sep;8(9):721-4. doi: 10.1038/sj.ejhg.5200521. Eur J Hum Genet. 2000. PMID: 10980580

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