Roncuzzi L - Search Results

1

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: roncuzzi l. Hum Genet. 1986 Sep;74(1):30-3. doi: 10.1007/BF00278781. Hum Genet. 1986. PMID: 3463531

2

Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.

Roncuzzi L, Fadda S, Mochi M, Prosperi L, Sangiorgi S, Santamaria R, Sbarra D, Besana D, Morandi L, Rocchi M, et al. Roncuzzi L, et al. Am J Hum Genet. 1985 Mar;37(2):407-17. Am J Hum Genet. 1985. PMID: 2984927 Free PMC article.

3

Mapping of human cellular retinol-binding protein to chromosome 3.

Colantuoni V, Rocchi M, Roncuzzi L, Romeo G. Colantuoni V, et al. Among authors: roncuzzi l. Cytogenet Cell Genet. 1986;43(3-4):221-2. doi: 10.1159/000132326. Cytogenet Cell Genet. 1986. PMID: 3802925

4

Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees.

Romeo G, Roncuzzi L, Sangiorgi S, Giacanelli M, Liguori M, Tessarolo D, Rocchi M. Romeo G, et al. Among authors: roncuzzi l. Hum Genet. 1988 Sep;80(1):59-62. doi: 10.1007/BF00451457. Hum Genet. 1988. PMID: 3417305

5

Origin of new mutations in Duchenne muscular dystrophy.

Roncuzzi L, Ferlini A, Pirozzi A, Romeo G. Roncuzzi L, et al. Hum Genet. 1986 Dec;74(4):456-60. doi: 10.1007/BF00280507. Hum Genet. 1986. PMID: 2878873

6

Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9).

Fadda S, Mochi M, Roncuzzi L, Sangiorgi S, Sbarra D, Zatz M, Romeo G. Fadda S, et al. Among authors: roncuzzi l. Hum Genet. 1985;71(1):33-6. doi: 10.1007/BF00295664. Hum Genet. 1985. PMID: 2993155

7

[New instruments in molecular genetics for the prevention of X chromosome-linked muscular dystrophy].

Ferlini A, Roncuzzi L, Romeo G. Ferlini A, et al. Among authors: roncuzzi l. Minerva Pediatr. 1986 Aug 31;38(15-16):639-42. Minerva Pediatr. 1986. PMID: 3796513 Italian. No abstract available.

8

X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms.

Romeo G, Rocchi M, Roncuzzi L, Ferlini A, Nobile C, Rugolo M. Romeo G, et al. Among authors: roncuzzi l. Adv Neurol. 1988;48:31-6. Adv Neurol. 1988. PMID: 2891257 Review. No abstract available.

9

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. Among authors: roncuzzi l. Lancet. 1988 Jul 2;2(8601):8-11. doi: 10.1016/s0140-6736(88)92943-1. Lancet. 1988. PMID: 2898665

10

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. Among authors: roncuzzi l. Eur J Pediatr. 1988 May;147(4):412-5. doi: 10.1007/BF00496422. Eur J Pediatr. 1988. PMID: 3165066

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