Journal of Human Genetics,volume 52,issue 9  (09-2007)

Period of time： 2007年9期

Publisher： Springer Publishing Company

Founded in： 1956

Total resources： 4

ISSN： 1434-5161

Subject： Q3 Genetics

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Journal of Human Genetics,volume 52,issue 9

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Polymorphisms and haplotypes of the gene encoding the estrogen-metabolizing CYP19 gene in Korean women: no association with advanced-stage endometriosis

By Hur Sung,Lee Sara,Lee Ji,Moon Hye-Sung,Kim Hyung,Chung Hye in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 703-711

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A comprehensive analysis of microsatellite diversity in Aboriginal Australians

By Walsh Simon in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 712-728

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Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples

By Marvelle Amanda,Lange Leslie,Qin Li,Wang Yunfei,Lange Ethan,Adair Linda,Mohlke Karen in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 729-737

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Identifying haplotype block structure using an ancestor-derived model

By Fujisawa Hironori,Isomura Minoru,Eguchi Shinto,Ushijima Masaru,Miyata Satoshi,Miki Yoshio,Matsuura Masaaki in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 738-746

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Entropy-based joint analysis for two-stage genome-wide association studies

By Kang Guolian,Zuo Yijun in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 747-756

Springer Publishing Company

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The association of common polymorphisms in the QPCT gene with bone mineral density in the Chinese population

By Huang Qing-Yang in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 757-762

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Y-chromosome haplogroup N dispersals from south Siberia to Europe

By Derenko Miroslava,Malyarchuk Boris,Denisova Galina,Wozniak Marcin,Grzybowski Tomasz,Dambueva Irina,Zakharov Ilia in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 763-770

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Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene

By Aquaron Robert,Soufir Nadem,Bergé-Lefranc Jean-Louis,Badens Catherine,Austerlitz Frederic,Grandchamp Bernard in (2007)

Journal of Human Genetics,volume 52,issue 9 , Vol. 52, Iss. 9, 2007-09 , pp. 771-780

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Total 8 item(s)