Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome)
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference25 articles.
1. Linkage analysis suggests at least two loci for X-linked nonspecific mental retardation
2. Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis
3. Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter
4. Norrie disease resulting from a gene deletion: clinical features and DNA studies.
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1. Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21;Clinical Genetics;2008-06-28
2. Human syndromes with congenital patellar anomalies and the underlying gene defects;Clinical Genetics;2005-09-02
3. Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family;Human Genetics;2003-02
4. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003
5. Gene for apparently nonsyndromic X‐linked mental retardation (MRX32) maps to an 18‐Mb region of Xp21.2‐p22;American Journal of Medical Genetics;1999-06-21
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