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Year | Number of Results |
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1993 | 1 |
2000 | 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.
Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.
Kozák L, Chiurazzi P, Genuardi M, Pomponi MG, Zollino M, Neri G.
Kozák L, et al.
J Med Genet. 1993 Oct;30(10):866-9. doi: 10.1136/jmg.30.10.866.
J Med Genet. 1993.
PMID: 8230164
Free PMC article.
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Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy.
Gohlke BC, Haug K, Fukami M, Friedl W, Noeker M, Rappold GA, Haverkamp F.
Gohlke BC, et al.
J Med Genet. 2000 Aug;37(8):600-2. doi: 10.1136/jmg.37.8.600.
J Med Genet. 2000.
PMID: 10922387
Free PMC article.
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