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Year | Number of Results |
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2000 | 1 |
2001 | 3 |
2003 | 1 |
2024 | 0 |
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Page 1
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region.
Hum Mol Genet. 2000 Feb 12;9(3):395-401. doi: 10.1093/hmg/9.3.395.
Hum Mol Genet. 2000.
PMID: 10655549
Complex events in the evolution of the human pseudoautosomal region 2 (PAR2).
Charchar FJ, Svartman M, El-Mogharbel N, Ventura M, Kirby P, Matarazzo MR, Ciccodicola A, Rocchi M, D'Esposito M, Graves JA.
Charchar FJ, et al.
Genome Res. 2003 Feb;13(2):281-6. doi: 10.1101/gr.390503.
Genome Res. 2003.
PMID: 12566406
Free PMC article.
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DHPLC analysis of the MECP2 gene in Italian Rett patients.
Nicolao P, Carella M, Giometto B, Tavolato B, Cattin R, Giovannucci-Uzielli ML, Vacca M, Della Regione F, Piva S, Bortoluzzi S, Gasparini P.
Nicolao P, et al.
Hum Mutat. 2001 Aug;18(2):132-40. doi: 10.1002/humu.1162.
Hum Mutat. 2001.
PMID: 11462237
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MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.
Vacca M, Filippini F, Budillon A, Rossi V, Della Ragione F, De Bonis ML, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, Macdonald F, Kerr A, Dhanjal S, Hulten M.
Vacca M, et al.
Brain Dev. 2001 Dec;23 Suppl 1:S246-50. doi: 10.1016/s0387-7604(01)00343-6.
Brain Dev. 2001.
PMID: 11738884
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Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.
Vacca M, Filippini F, Budillon A, Rossi V, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, MacDonald F, Kerr A, Dhanjal S, Hultén M.
Vacca M, et al.
J Mol Med (Berl). 2001;78(11):648-55. doi: 10.1007/s001090000155.
J Mol Med (Berl). 2001.
PMID: 11269512
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