13 results on '"Bakker, E."'
Search Results
2. X-chromosome duplications in males with mental retardation: pathogenic or benign variants?
3. Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy
4. Asymptomatic and late-onset ornithine transcarbamylase (OTC) deficiency in males of a five-generation family, caused by an A208T mutation
5. X-chromosome duplications in males with mental retardation: pathogenic or benign variants?
6. Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?
7. Asymptomatic and late-onset ornithine transcarbamylase (OTC) deficiency in males of a five-generation family, caused by an A208T mutation
8. Mutation of the Duchenne muscular dystrophy gene associated with meiotic recombination
9. Carrier detection in X‐linked ocular albinism of the Nettleship‐Falls type by DNA analysis
10. Asymptomatic and late-onset ornithine transcarbamylase (OTC) deficiency in males of a five-generation family, caused by an A208T mutation.
11. Mutation of the Duchenne muscular dystrophy gene associated with meiotic recombination.
12. Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis.
13. Orientation of major histocompatibility (MHC) genes relative to the centromere of human chromosome 6.
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