A 6-Mb YAC contig in Xp22.1–p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference60 articles.
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1. Genetic background of HSH in three Polish families and a patient with an X;9 translocation;European Journal of Human Genetics;2005-11-02
2. Physical and Transcript Map of a 2-Mb Region in Xp22.1 Containing Candidate Genes for X-linked Mental Retardation and Short Stature;Genomics;2002-03
3. Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland;European Journal of Human Genetics;1999-04
4. Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22;Genomics;1999-02
5. The isolation of CpG islands from human chromosomal regions 11q13 and Xp22 by segregation of partlymelted molecules;Nucleic Acids Research;1998-12-15
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