Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb02622.x/fullpdf
Reference49 articles.
1. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation;Arveiler;Am J Med Genet,1988
2. Regional localisation of a non-specific X-linked mental retardation gene (MRX 19) to Xp22;Donnelly;Am J Med Genet,1994
3. A Technique for radiolabeling DNA restriction endonuc lease fragments to high specific activity;Feinberg;Anal Biochem,1983
4. Genetic localisation of MRX27 to Xq24-26 defines the sixth discrete gene for non-specific X-linked mental retardation;Gedeon;Am J Med Genet,1996
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3. X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation;Genome Research;2007-04-06
4. XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene;BMC Medical Genetics;2005-04-25
5. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003
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