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Volume 52; Issue 9
Main
Journal of Human Genetics
Volume 52; Issue 9
Journal of Human Genetics
Volume 52; Issue 9
1
A comprehensive analysis of microsatellite diversity in Aboriginal Australians
Simon J. Walsh
,
R. John Mitchell
,
Natalie Watson
,
John S. Buckleton
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 679 KB
Your tags:
english, 2007
2
Polymorphisms and haplotypes of the gene encoding the estrogen-metabolizing CYP19 gene in Korean women: no association with advanced-stage endometriosis
Sung Eun Hur
,
Sara Lee
,
Ji Young Lee
,
Hye-Sung Moon
,
Hyung Lae Kim
,
Hye Won Chung
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 166 KB
Your tags:
english, 2007
3
Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples
Amanda F. Marvelle
,
Leslie A. Lange
,
Li Qin
,
Yunfei Wang
,
Ethan M. Lange
,
Linda S. Adair
,
Karen L. Mohlke
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 244 KB
Your tags:
english, 2007
4
Identifying haplotype block structure using an ancestor-derived model
Hironori Fujisawa
,
Minoru Isomura
,
Shinto Eguchi
,
Masaru Ushijima
,
Satoshi Miyata
,
Yoshio Miki
,
Masaaki Matsuura
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 259 KB
Your tags:
english, 2007
5
Entropy-based joint analysis for two-stage genome-wide association studies
Guolian Kang
,
Yijun Zuo
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 389 KB
Your tags:
english, 2007
6
The association of common polymorphisms in theQPCTgene with bone mineral density in the Chinese population
Qing-Yang Huang
,
Annie W. C. Kung
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 176 KB
Your tags:
english, 2007
7
Y-chromosome haplogroup N dispersals from south Siberia to Europe
Miroslava Derenko
,
Boris Malyarchuk
,
Galina Denisova
,
Marcin Wozniak
,
Tomasz Grzybowski
,
Irina Dambueva
,
Ilia Zakharov
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 374 KB
Your tags:
english, 2007
8
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
Robert Aquaron
,
Nadem Soufir
,
Jean-Louis Bergé-Lefranc
,
Catherine Badens
,
Frederic Austerlitz
,
Bernard Grandchamp
Journal:
Journal of Human Genetics
Year:
2007
Language:
english
File:
PDF, 228 KB
Your tags:
english, 2007
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