Neri G - Search Results

1

Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at the D5S524 locus.

Velonà I, Zappata S, Tops CM, Fodde R, Khan PM, Neri G, Brahe C. Velonà I, et al. Among authors: neri g. Hum Mol Genet. 1993 Jun;2(6):829. doi: 10.1093/hmg/2.6.829-a. Hum Mol Genet. 1993. PMID: 8353514 No abstract available.

2

PCR detection of an insertion/deletion polymorphism in intron 1 of the HRAS1 locus.

Tanci P, Genuardi M, Santini SA, Neri G. Tanci P, et al. Among authors: neri g. Nucleic Acids Res. 1992 Mar 11;20(5):1157. doi: 10.1093/nar/20.5.1157. Nucleic Acids Res. 1992. PMID: 1549493 Free PMC article.

3

Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction.

Serra A, Brahe C, Millington-Ward A, Neri G, Tedeschi B, Tassone F, Bova R. Serra A, et al. Among authors: neri g. Am J Med Genet Suppl. 1990;7:162-8. doi: 10.1002/ajmg.1320370733. Am J Med Genet Suppl. 1990. PMID: 1981475

4

Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy.

Brahe C, Servidei S, Zappata S, Ricci E, Tonali P, Neri G. Brahe C, et al. Among authors: neri g. Lancet. 1995 Sep 16;346(8977):741-2. doi: 10.1016/s0140-6736(95)91507-9. Lancet. 1995. PMID: 7658877

5

Unstable triplets and their mutational mechanism: size reduction of the CGG repeat vs. germline mosaicism in the fragile X syndrome.

Chiurazzi P, Kozak L, Neri G. Chiurazzi P, et al. Among authors: neri g. Am J Med Genet. 1994 Jul 15;51(4):517-21. doi: 10.1002/ajmg.1320510446. Am J Med Genet. 1994. PMID: 7943033 Review.

6

Identification of key recombinants in multiplex SMA families.

van der Steege G, Cobben JM, Brahe C, Osinga J, Zappata S, Scheffer H, Neri G, van Ommen GJ, ten Kate LP, Buys CH. van der Steege G, et al. Among authors: neri g. Genomics. 1994 Jul 1;22(1):219-22. doi: 10.1006/geno.1994.1367. Genomics. 1994. PMID: 7959774

7

Presymptomatic diagnosis of SMA III by genotype analysis.

Brahe C, Zappata S, Velonà I, Bertini E, Servidei S, Tonali P, Neri G. Brahe C, et al. Among authors: neri g. Am J Med Genet. 1993 Feb 1;45(3):408-11. doi: 10.1002/ajmg.1320450331. Am J Med Genet. 1993. PMID: 8434634

8

Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.

Sebastio G, Perone L, Guzzetta V, Sebastio L, Vicari L, Della Casa R, Gurrieri F, Zappata S, Pomponi MG, Mazzei A, Neri G, Andria G, Brahe C. Sebastio G, et al. Among authors: neri g. Am J Med Genet. 1996 May 17;63(2):366-72. doi: 10.1002/(SICI)1096-8628(19960517)63:2<366::AID-AJMG8>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8725787

9

Deletions in the SMN gene in infantile and adult spinal muscular atrophy patients from the same family.

Zappata S, Tiziano F, Neri G, Brahe C. Zappata S, et al. Among authors: neri g. Hum Genet. 1996 Mar;97(3):315-8. doi: 10.1007/BF02185762. Hum Genet. 1996. PMID: 8786072

10

Frameshift mutation in the survival motor neuron gene in a severe case of SMA type I.

Brahe C, Clermont O, Zappata S, Tiziano F, Melki J, Neri G. Brahe C, et al. Among authors: neri g. Hum Mol Genet. 1996 Dec;5(12):1971-6. doi: 10.1093/hmg/5.12.1971. Hum Mol Genet. 1996. PMID: 8968751

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