Neri G - Search Results

1

Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.

Genuardi M, Pomponi MG, Sammito V, Bellussi A, Zollino M, Neri G. Genuardi M, et al. Among authors: neri g. Am J Med Genet. 1993 Nov 1;47(6):823-31. doi: 10.1002/ajmg.1320470606. Am J Med Genet. 1993. PMID: 8279479

2

Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.

Gurrieri F, Cappa M, Neri G. Gurrieri F, et al. Among authors: neri g. Am J Med Genet. 1992 Sep 15;44(2):136-7. doi: 10.1002/ajmg.1320440203. Am J Med Genet. 1992. PMID: 1456280

3

New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.

Gurrieri F, Sammito V, Bellussi A, Neri G. Gurrieri F, et al. Among authors: neri g. Am J Med Genet. 1992 Oct 1;44(3):315-20. doi: 10.1002/ajmg.1320440310. Am J Med Genet. 1992. PMID: 1488978 No abstract available.

4

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.

5

Possible new type of oral-facial-digital syndrome with retinal abnormalities: OFDS type (VIII).

Gurrieri F, Sammito V, Ricci B, Iossa M, Bellussi A, Neri G. Gurrieri F, et al. Among authors: neri g. Am J Med Genet. 1992 Apr 1;42(6):789-92. doi: 10.1002/ajmg.1320420608. Am J Med Genet. 1992. PMID: 1554016

6

XLMR genes: update 1992.

Neri G, Chiurazzi P, Arena F, Lubs HA, Glass IA. Neri G, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):373-82. doi: 10.1002/ajmg.1320430158. Am J Med Genet. 1992. PMID: 1605215 Review.

7

New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria.

Zollino M, Mastroiacovo P, Zampino G, Mariotti P, Neri G. Zollino M, et al. Among authors: neri g. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):452-7. doi: 10.1002/ajmg.1320430168. Am J Med Genet. 1992. PMID: 1605225

8

Dosage analysis at the CSF1 and CSF1R loci in a new case of partial trisomy 5q.

Genuardi M, Flamia R, Palka G, Parruti G, Neri G. Genuardi M, et al. Among authors: neri g. Clin Genet. 1992 May;41(5):259-62. doi: 10.1111/j.1399-0004.1992.tb03677.x. Clin Genet. 1992. PMID: 1606715

9

An additional patient with the 3C syndrome.

Gurrieri F, Neri G. Gurrieri F, et al. Among authors: neri g. Clin Genet. 1992 May;41(5):263-5. doi: 10.1111/j.1399-0004.1992.tb03678.x. Clin Genet. 1992. PMID: 1606716

10

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

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