Human Genetics,volume 129,issue 2  (02-2011)

Period of time: 2011年2期

Publisher: Springer Publishing Company

Founded in: 1913

Total resources: 46

ISSN: 0340-6717

Subject: Q3 Genetics

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Human Genetics,volume 129,issue 2

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Molecular cloning of two novel mucin-like genes in the disease-susceptibility locus for diffuse panbronchiolitis

By Hijikata Minako,Matsushita Ikumi,Tanaka Goh,Tsuchiya Tomoko,Ito Hideyuki,Tokunaga Katsushi,Ohashi Jun,Homma Sakae,Kobashi Yoichiro,Taguchi Yoshio,Azuma Arata,Kudoh Shoji,Keicho Naoto in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 117-128

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polymorphisms are associated with risk for metabolic syndrome

By Devaney Joseph,Gordish-Dressman Heather,Harmon Brennan,Bradbury Margaret,Devaney Stephanie,Harris Tamara,Thompson Paul,Clarkson Priscilla,Price Thomas,Angelopoulos Theodore,Gordon Paul,Moyna Niall,Pescatello Linda,Visich Paul,Zoeller Robert,Seip Richard,Seo Jinwook,Kim Bo,Tosi Laura,Garcia Melissa,Li Rongling,Zmuda Joseph,Delmonico Matthew,Lindsay Robert,Howard Barbara,Kraus William,Hoffman Eric in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 129-139

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Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots

By Kuss Andreas,Garshasbi Masoud,Kahrizi Kimia,Tzschach Andreas,Behjati Farkhondeh,Darvish Hossein,Abbasi-Moheb Lia,Puettmann Lucia,Zecha Agnes,Weißmann Robert,Hu Hao,Mohseni Marzieh,Abedini Seyedeh,Rajab Anna,Hertzberg Christoph,Wieczorek Dagmar,Ullmann Reinhard,Ghasemi-Firouzabadi Saghar,Banihashemi Susan,Arzhangi Sanaz,Hadavi Valeh,Bahrami-Monajemi Gholamreza,Kasiri Mahboubeh,Falah Masoumeh,Nikuei Pooneh,Dehghan Atefeh,Sobhani Masoumeh,Jamali Payman,Ropers Hans,Najmabadi Hossein in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 141-148

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Modifier locus of the skeletal muscle involvement in Emery–Dreifuss muscular dystrophy

By Granger B.,Gueneau L.,Drouin-Garraud V.,Pedergnana V.,Gagnon F.,Ben Yaou R.,Tezenas du Montcel S.,Bonne G. in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 149-159

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Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence

By Culverhouse Robert,Saccone Nancy,Stitzel Jerry,Wang Jen,Steinbach Joseph,Goate Alison,Schwantes-An Tae-Hwi,Grucza Richard,Stevens Victoria,Bierut Laura in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 177-188

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High resolution mapping of intragenic rearrangements and identification of a founder effect associated with a deletion in Polish albino patients

By Rooryck Caroline,Morice-Picard Fanny,Lasseaux Eulalie,Cailley Dorothée,Dollfus Hélène,Defoort-Dhellemme Sabine,Duban-Bedu Bénédicte,Ravel Thomy,Taieb Alain,Lacombe Didier,Arveiler Benoît in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 199-208

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Genome-wide linkage and peak-wide association study of obesity-related quantitative traits in Caribbean Hispanics

By Dong Chuanhui,Beecham Ashley,Slifer Susan,Wang Liyong,McClendon Mark,Blanton Susan,Rundek Tatjana,Sacco Ralph in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 209-219

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Genetic risk sum score comprised of common polygenic variation is associated with body mass index

By Peterson Roseann,Maes Hermine,Holmans Peter,Sanders Alan,Levinson Douglas,Shi Jianxin,Kendler Kenneth,Gejman Pablo,Webb Bradley in (2011)

Human Genetics,volume 129,issue 2 , Vol. 129, Iss. 2, 2011-02 , pp. 221-230

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