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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Disease and GLB1[original query]
Population analysis of the GLB1 gene in South Brazil.
Genetics and molecular biology 2011 Jan 34 (1): 45-8.
Baiotto Cléia, Sperb Fernanda, Matte Ursula, da Silva Cláudia Dornelles, Sano Renata, Coelho Janice Carneiro, Giugliani Rober
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population. GWAS Catalog
Nature genetics 2012 Nov 44 (11): 1222-6.
Hirota Tomomitsu, Takahashi Atsushi, Kubo Michiaki, Tsunoda Tatsuhiko, Tomita Kaori, Sakashita Masafumi, Yamada Takechiyo, Fujieda Shigeharu, Tanaka Shota, Doi Satoru, Miyatake Akihiko, Enomoto Tadao, Nishiyama Chiharu, Nakano Nobuhiro, Maeda Keiko, Okumura Ko, Ogawa Hideoki, Ikeda Shigaku, Noguchi Emiko, Sakamoto Tohru, Hizawa Nobuyuki, Ebe Koji, Saeki Hidehisa, Sasaki Takashi, Ebihara Tamotsu, Amagai Masayuki, Takeuchi Satoshi, Furue Masutaka, Nakamura Yusuke, Tamari Mayu
Prevalence and Novel Mutations of Lysosomal Storage Disorders in United Arab Emirates : LSD in UAE.
JIMD reports 2013 10 1-9.
Al-Jasmi Fatma A, Tawfig Nafisa, Berniah Ans, Ali Bassam R, Taleb Mahmoud, Hertecant Jozef L, Bastaki Fatma, Souid Abdul-Kad
Rapid Targeted Genomics in Critically Ill Newborns.
Pediatrics 2017 9 140 (4): .
van Diemen Cleo C, Kerstjens-Frederikse Wilhelmina S, Bergman Klasien A, de Koning Tom J, Sikkema-Raddatz Birgit, van der Velde Joeri K, Abbott Kristin M, Herkert Johanna C, Löhner Katharina, Rump Patrick, Meems-Veldhuis Martine T, Neerincx Pieter B T, Jongbloed Jan D H, van Ravenswaaij-Arts Conny M, Swertz Morris A, Sinke Richard J, van Langen Irene M, Wijmenga Cis
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients.
PloS one 2018 2 13 (2): e0188869.
Ji Haoran, Li Dongxiao, Wu Ye, Zhang Quanli, Gu Qiang, Xie Han, Ji Taoyun, Wang Huifang, Zhao Lu, Zhao Haijuan, Yang Yanling, Feng Hongchun, Xiong Hui, Ji Jinhua, Yang Zhixian, Kou Liping, Li Ming, Bao Xinhua, Chang Xingzhi, Zhang Yuehua, Li Li, Li Huijuan, Niu Zhengping, Wu Xiru, Xiao Jiangxi, Jiang Yuwu, Wang Jingm
Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis.
Clinical neurology and neurosurgery 2018 2 167 43-53.
Mahdieh Nejat, Mikaeeli Sahar, Tavasoli Ali Reza, Rezaei Zahra, Maleki Majid, Rabbani Bahar
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