in J Med Genet during October 2009 -- updated monthly
These articles have received the most "hits" in Journal of Medical Genetics during October 2009.
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| 6. | Y Qiao, N Riendeau, M Koochek, X Liu, Chansonette Harvard, M J Hildebrand, J J A Holden, E Rajcan-Separovic, M E S Lewis | ||
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Phenomic determinants of genomic variation in autism spectrum disorders | |
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J. Med. Genet. 2009; 46: 680-688.
(In "Original articles") |
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| 7. | L Roos, A E Jønch, S Kjaergaard, K Taudorf, H Simonsen, B Hamborg-Petersen, K Brøndum-Nielsen, M Kirchhoff | ||
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A new microduplication syndrome encompassing the region of the Miller–Dieker (17p13 deletion) syndrome | |
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J. Med. Genet. 2009; 46: 703-710.
(In "Letters to JMG") |
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| 8. | S M Maas, M P Lombardi, A J van Essen, E L Wakeling, B Castle, I K Temple, V K A Kumar, K Writzl, Raoul C M Hennekam | ||
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Phenotype and genotype in 17 patients with Goltz–Gorlin syndrome | |
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J. Med. Genet. 2009; 46: 716-720.
(In "Mutation report") |
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| 9. | K D Gonzalez, C H Buzin, K A Noltner, D Gu, W Li, D Malkin, S S Sommer | ||
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High frequency of de novo mutations in Li–Fraumeni syndrome | |
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J. Med. Genet. 2009; 46: 689-693.
(In "Letters to JMG") |
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| 10. | J Gu, J Huang, C Li, L Zhao, F Huang, Z Liao, T Li, Q Wei, Z Lin, Y Pan, J Huang, X Wang, Q Lin, C Lu, Y Wu, S Cao, J Wu, H Xu, B Yu, Y Shen | ||
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Association of chromosome 2q36.1–36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families | |
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J. Med. Genet. 2009; 46: 657-662.
(In "Original articles") |
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| [Previous 5 Articles] | |||
= from the current issue
Last Updated: 11/05/2009 10:04:16
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