Neri G - Search Results

1

New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndrome.

Reynolds JF, Neri G, Herrmann JP, Blumberg B, Coldwell JG, Miles PV, Opitz JM. Reynolds JF, et al. Among authors: neri g. Am J Med Genet. 1986 Nov;25(3):413-27. doi: 10.1002/ajmg.1320250303. Am J Med Genet. 1986. PMID: 3789005

2

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.

3

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

4

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

5

Fifth international workshop on fragile X and X-linked mental retardation.

Mandel JL, Hagerman R, Froster U, Brown WT, Jenkins EC, Jacobs P, TurnerG, Lubs H, Neri G. Mandel JL, et al. Among authors: neri g. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):5-27. doi: 10.1002/ajmg.1320430104. Am J Med Genet. 1992. PMID: 1605233 No abstract available.

6

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

7

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

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: 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

9

Encomium and dedication: Angelo Serra--four decades in human and medical genetics.

Neri G, Opitz JM. Neri G, et al. Am J Med Genet Suppl. 1990;7:5-8. Am J Med Genet Suppl. 1990. PMID: 2149973 No abstract available.

10

"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.

Lalatta F, Clerici Bagozzi D, Salmoiraghi MG, Tagliabue P, Tischer C, Zollino M, Di Rocco C, Neri G, Opitz JM. Lalatta F, et al. Among authors: neri g. Am J Med Genet. 1990 Dec;37(4):451-6. doi: 10.1002/ajmg.1320370404. Am J Med Genet. 1990. PMID: 2260586

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