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Year | Number of Results |
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2000 | 1 |
2001 | 1 |
2002 | 2 |
2024 | 0 |
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A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.
Am J Hum Genet. 2000 Sep;67(3):563-73. doi: 10.1086/303047. Epub 2000 Jul 20.
Am J Hum Genet. 2000.
PMID: 10903929
Free PMC article.
IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervous system.
Ferrante MI, Ghiani M, Bulfone A, Franco B.
Ferrante MI, et al.
Gene. 2001 Sep 19;275(2):217-21. doi: 10.1016/s0378-1119(01)00659-x.
Gene. 2001.
PMID: 11587848
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Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.
Toutain A, Dessay B, Ronce N, Ferrante MI, Tranchemontagne J, Newbury-Ecob R, Wallgren-Pettersson C, Burn J, Kaplan J, Rossi A, Russo S, Walpole I, Hartsfield JK, Oyen N, Nemeth A, Bitoun P, Trump D, Moraine C, Franco B.
Toutain A, et al.
Eur J Hum Genet. 2002 Sep;10(9):516-20. doi: 10.1038/sj.ejhg.5200846.
Eur J Hum Genet. 2002.
PMID: 12173028
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Oral, facial, digital, vertebral anomalies with psychomotor delay: a mild form of OFD type Gabrielli?
Ferrero GB, Valenzise M, Franco B, Defilippi C, Gregato G, Corsello G, Pepe E, Silengo M.
Ferrero GB, et al.
Am J Med Genet. 2002 Dec 1;113(3):291-4. doi: 10.1002/ajmg.10815.
Am J Med Genet. 2002.
PMID: 12439899
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