Neri G - Search Results

1

A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer.

Lucci-Cordisco E, Zollino M, Baglioni S, Mancuso I, Lecce R, Gurrieri F, Crucitti A, Papi L, Neri G, Genuardi M. Lucci-Cordisco E, et al. Among authors: neri g. Clin Genet. 2005 Feb;67(2):178-82. doi: 10.1111/j.1399-0004.2004.00390.x. Clin Genet. 2005. PMID: 15679831

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

The Noonan-CFC controversy.

Neri G, Zollino M, Reynolds JF. Neri G, et al. Am J Med Genet. 1991 Jun 1;39(3):367-70. doi: 10.1002/ajmg.1320390323. Am J Med Genet. 1991. PMID: 1867292

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