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MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation. [electronic resource] by
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- Gendrot, Chantal
- Verloes, Alain
- Raynaud, Martine
- David, Albert
- Yntema, Helger G
- Dessay, Sabine
- Kalscheuer, Vera
- Frints, Suzanne
- Couvert, Philippe
- Briault, Sylvain
- Blesson, Sophie
- Toutain, Annick
- Chelly, Jamel
- Desportes, Vincent
- Moraine, Claude
Producer: 20040716
In:
American journal of medical genetics. Part A vol. 123A
Availability: No items available.
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442.
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443.
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Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants. [electronic resource] by
- Lawrence, Robert
- Evans, David M
- Morris, Andrew P
- Ke, Xiayi
- Hunt, Sarah
- Paolucci, Marta
- Ragoussis, Jiannis
- Deloukas, Panos
- Bentley, David
- Cardon, Lon R
Producer: 20060502
In:
Genome research vol. 15
Availability: No items available.
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451.
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452.
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Recombinant yeast screen for new inhibitors of human acetyl-CoA carboxylase 2 identifies potential drugs to treat obesity. [electronic resource] by
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- Chalupska, Dominika
- Patenode, Caroline
- Coster, Adam
- Arnold, Evan
- Ye, Alice
- Anesi, George
- Lu, Ying
- Okun, Ilya
- Tkachenko, Sergey
- Haselkorn, Robert
- Gornicki, Piotr
Producer: 20100722
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 107
Availability: No items available.
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