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XLMR genes: update 2000.
Chiurazzi P, Hamel BC, Neri G. Chiurazzi P, et al. Among authors: neri g. Eur J Hum Genet. 2001 Feb;9(2):71-81. doi: 10.1038/sj.ejhg.5200603. Eur J Hum Genet. 2001. PMID: 11313739 Review.
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
Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.
Neri G, Marini R, Cappa M, Borrelli P, Opitz JM. Neri G, et al. Am J Med Genet. 1988 May-Jun;30(1-2):287-99. doi: 10.1002/ajmg.1320300130. Am J Med Genet. 1988. PMID: 3177455
Fragile X expression in normal and mentally retarded subjects: effect of treatment with an antifolic agent.
Sanfilippo S, Ragusa RM, Scillato F, Ruggeri M, Neri G. Sanfilippo S, et al. Among authors: neri g. Am J Med Genet. 1988 May-Jun;30(1-2):369-76. doi: 10.1002/ajmg.1320300137. Am J Med Genet. 1988. PMID: 3177459
The CFC syndrome--report of the first two cases outside the United States.
Neri G, Sabatino G, Bertini E, Genuardi M. Neri G, et al. Am J Med Genet. 1987 Aug;27(4):767-71. doi: 10.1002/ajmg.1320270404. Am J Med Genet. 1987. PMID: 3425595
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.
Chiurazzi P, de Graaff E, Ng J, Verkerk AJ, Wolfson S, Fisch GS, Kozak L, Neri G, Oostra BA. Chiurazzi P, et al. Among authors: neri g. Am J Med Genet. 1994 Jul 15;51(4):309-14. doi: 10.1002/ajmg.1320510405. Am J Med Genet. 1994. PMID: 7942992
A split hand-split foot (SHFM3) gene is located at 10q24-->25.
Gurrieri F, Prinos P, Tackels D, Kilpatrick MW, Allanson J, Genuardi M, Vuckov A, Nanni L, Sangiorgi E, Garofalo G, Nunes ME, Neri G, Schwartz C, Tsipouras P. Gurrieri F, et al. Among authors: neri g. Am J Med Genet. 1996 Apr 24;62(4):427-36. doi: 10.1002/(SICI)1096-8628(19960424)62:4<427::AID-AJMG16>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8723077
Novel findings in a patient with Weaver or a Weaver-like syndrome.
Scarano G, Della Monica M, Lonardo F, Neri G. Scarano G, et al. Among authors: neri g. Am J Med Genet. 1996 May 17;63(2):378-81. doi: 10.1002/(SICI)1096-8628(19960517)63:2<378::AID-AJMG10>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8725789
Cardio-facio-cutaneous (CFC) syndrome: report of an adult without mental retardation.
Manoukian S, Lalatta F, Selicorni A, Tadini G, Cavalli R, Neri G. Manoukian S, et al. Among authors: neri g. Am J Med Genet. 1996 May 17;63(2):382-5. doi: 10.1002/(SICI)1096-8628(19960517)63:2<382::AID-AJMG11>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8725790
XLMR genes: update 1996.
Lubs HA, Chiurazzi P, Arena JF, Schwartz C, Tranebjaerg L, Neri G. Lubs HA, et al. Among authors: neri g. Am J Med Genet. 1996 Jul 12;64(1):147-57. doi: 10.1002/(SICI)1096-8628(19960712)64:1<147::AID-AJMG25>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826465 Review.
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