Gene Conversion in Evolution and Disease
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470015902.a0005100.pub2
Reference71 articles.
1. Hemoglobin Parchman: Double Crossover Within a Single Human Gene
2. A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics
3. Lower-Than-Expected Linkage Disequilibrium between Tightly Linked Markers in Humans Suggests a Role for Gene Conversion
4. Novel biallelic mutations inMSH6 andPMS2 genes: gene conversion as a likely cause ofPMS2 gene inactivation
5. Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism
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