Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference6 articles.
1. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14
2. A possible explanation for the low incidence of gonosomal aneuploidy among the offspring of triplo-X individuals
3. International workshop on the fragile X and X-linked mental retardation
4. Second international workshop on the fragile X and on X-linked mental retardation
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