Neri G - Search Results

1

Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog.

Garavelli L, Zanacca C, Caselli G, Banchini G, Dubourg C, David V, Odent S, Gurrieri F, Neri G. Garavelli L, et al. Among authors: neri g. Am J Med Genet A. 2004 May 15;127A(1):93-95. doi: 10.1002/ajmg.a.20685. Am J Med Genet A. 2004. PMID: 15103725

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

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

5

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

6

XLMR genes: update 1990.

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

7

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: neri g. Am J Med Genet. 1991 Feb-Mar;38(2-3):228-32. doi: 10.1002/ajmg.1320380211. Am J Med Genet. 1991. PMID: 2018063

8

A girl with the Lujan-Fryns syndrome.

Gurrieri F, Neri G. Gurrieri F, et al. Among authors: neri g. 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.

9

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. Among authors: neri g. Am J Med Genet. 1995 Jan 30;55(3):315-8. doi: 10.1002/ajmg.1320550314. Am J Med Genet. 1995. PMID: 7726229

10

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini R, Scarano G, Cappa M, Neri G. Zollino M, et al. Among authors: neri g. Am J Med Genet. 1994 Sep 1;52(3):302-7. doi: 10.1002/ajmg.1320520310. Am J Med Genet. 1994. PMID: 7810561

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