Novelli G - Search Results

1

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

Wadey R, McKie J, Papapetrou C, Sutherland H, Lohman F, Osinga J, Frohn I, Hofstra R, Meijers C, Amati F, Conti E, Pizzuti A, Dallapiccola B, Novelli G, Scambler P. Wadey R, et al. Among authors: novelli g. Am J Hum Genet. 1999 Jul;65(1):247-9. doi: 10.1086/302468. Am J Hum Genet. 1999. PMID: 10364538 Free PMC article. No abstract available.

2

Genotyping of spinal muscular atrophy families with linked DNA probes.

Gennarelli M, Melchionda S, Fattorini C, Novelli G, Dallapiccola B. Gennarelli M, et al. Among authors: novelli g. Clin Genet. 1992 Dec;42(6):317-9. doi: 10.1111/j.1399-0004.1992.tb03264.x. Clin Genet. 1992. PMID: 1362926

3

Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridization.

Couillin P, Zucman J, Le Guern E, Reguigne I, Grisard MC, Delattre O, Novelli G, Dallapiccola B, Boué A. Couillin P, et al. Among authors: novelli g. Ann Genet. 1992;35(3):140-5. Ann Genet. 1992. PMID: 1466562

4

The cystic fibrosis delta F508 mutation in the Albanian population.

Novelli G, Sangiuolo F, Mokini V, Cikuli M, Piazza A, Dallapiccola B. Novelli G, et al. Am J Hum Genet. 1992 Apr;50(4):875-6. Am J Hum Genet. 1992. PMID: 1550133 Free PMC article. No abstract available.

5

Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction.

Novelli G, Gennarelli M, Rocchi M, Dallapiccola B. Novelli G, et al. Hum Genet. 1992 Mar;88(6):697-8. doi: 10.1007/BF02265301. Hum Genet. 1992. PMID: 1551677 No abstract available.

6

3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.

Gennarelli M, Novelli G, Cobo A, Baiget M, Dallapiccola B. Gennarelli M, et al. Among authors: novelli g. Hum Genet. 1991 Oct;87(6):654-6. doi: 10.1007/BF00201719. Hum Genet. 1991. PMID: 1682233

7

PCR DNA typing for forensics.

Dallapiccola B, Novelli G, Spinella A. Dallapiccola B, et al. Among authors: novelli g. Nature. 1991 Nov 21;354(6350):179. doi: 10.1038/354179a0. Nature. 1991. PMID: 1961246 No abstract available.

8

Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families.

Novelli G, Gasparini P, Savoia A, Pignatti PF, Sangiuolo F, Dallapiccola B. Novelli G, et al. Hum Genet. 1990 Sep;85(4):420-1. doi: 10.1007/BF02428291. Hum Genet. 1990. PMID: 2210757

9

A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.

Abbas N, Novelli G, Stella NC, Triolo O, Corrado F, Fellous M, Chery M, Gilgenkrantz S, Dallapiccola B. Abbas N, et al. Among authors: novelli g. Hum Genet. 1990 Nov;86(1):94-8. doi: 10.1007/BF00205184. Hum Genet. 1990. PMID: 2253943

10

PCR amplification and silver stain detection of genomic DNA fragments.

Novelli G, Mannello F, Dallapiccola B. Novelli G, et al. Trends Genet. 1989 Sep;5(9):293. doi: 10.1016/0168-9525(89)90109-1. Trends Genet. 1989. PMID: 2480012 No abstract available.

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