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[Although genotype-phenotype correlations in male patients with various types of nullisomy for Xp22.3 have assigned a locus for X-linked mental retardation (MRX) to an approximately 3-Mb region between DXS31 and STS, the precise location has not been determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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