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I M MacDonald

Showing results (61-70 of 63) with videos related to

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Clinical Genetics|July 13, 2010
A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disordersA M Innes, K M Boycott, E G Puffenberger, et al.
Nature Genetics|January 4, 2001
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophyK Zhang, M Kniazeva, M Han, et al.
Nature Communications|January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindnessS Kmoch, J Majewski, V Ramamurthy, et al.
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Showing results (61-70 of 63) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 63 results.
Clinical Genetics|July 13, 2010
A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disordersA M Innes, K M Boycott, E G Puffenberger, et al.
Nature Genetics|January 4, 2001
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophyK Zhang, M Kniazeva, M Han, et al.
Nature Communications|January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindnessS Kmoch, J Majewski, V Ramamurthy, et al.
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