Gurrieri F - 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: gurrieri f. Clin Genet. 2005 Feb;67(2):178-82. doi: 10.1111/j.1399-0004.2004.00390.x. Clin Genet. 2005. PMID: 15679831

2

Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders.

Lintas C, Cassano I, Azzarà A, Stigliano MG, Gregorj C, Sacco R, Stoccoro A, Coppedè F, Gurrieri F. Lintas C, et al. Among authors: gurrieri f. Genes (Basel). 2023 Feb 25;14(3):585. doi: 10.3390/genes14030585. Genes (Basel). 2023. PMID: 36980856 Free PMC article.

3

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

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

4

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. 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.

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. Am J Med Genet. 1992 Apr 1;42(6):789-92. doi: 10.1002/ajmg.1320420608. Am J Med Genet. 1992. PMID: 1554016

6

An additional patient with the 3C syndrome.

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

7

XLMR genes: update 1990.

Neri G, Gurrieri F, Gal A, Lubs HA. Neri G, et al. Among authors: gurrieri f. Am J Med Genet. 1991 Feb-Mar;38(2-3):186-9. doi: 10.1002/ajmg.1320380204. Am J Med Genet. 1991. PMID: 2018056

8

X-linked mental retardation with marfanoid habitus: first report of four Italian patients.

Lalatta F, Livini E, Selicorni A, Briscioli V, Vita A, Lugo F, Zollino M, Gurrieri F, Neri G. Lalatta F, et al. Among authors: gurrieri f. Am J Med Genet. 1991 Feb-Mar;38(2-3):228-32. doi: 10.1002/ajmg.1320380211. Am J Med Genet. 1991. PMID: 2018063

9

A girl with the Lujan-Fryns syndrome.

Gurrieri F, Neri G. Gurrieri F, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):290-1. doi: 10.1002/ajmg.1320380225. Am J Med Genet. 1991. PMID: 2018074 No abstract available.

10

Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: further evidence for the existence of a limb defect gene in 6q21.

Gurrieri F, Cammarata M, Avarello RM, Genuardi M, Pomponi MG, Neri G, Giuffrè L. Gurrieri F, et al. Am J Med Genet. 1995 Jan 30;55(3):315-8. doi: 10.1002/ajmg.1320550314. Am J Med Genet. 1995. PMID: 7726229

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