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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 ARX[original query]
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders.
Psychiatric genetics 2008 Dec 18 (6): 295-301.
Laroche Fabrice, Ramoz Nicolas, Leroy Sophie, Fortin Célia, Rousselot-Paillet Bérangère, Philippe Anne, Colleaux Laurence, Bresson Jean-Louis, Mogenet Agnès, Golse Bernard, Mouren-Simeoni Marie-Christine, Gorwood Philip, Galli Thierry, Simonneau Michel, Krebs Marie-Odile, Robel Lauren
Mutations of ARX and non-syndromic intellectual disability in Chinese population.
Genes & genomics 2018 Sep .
Wu Yufei, Zhang Huan, Liu Xiaofen, Shi Zhangyan, Li Hongling, Wang Zhibin, Jie Xiaoyong, Huang Shaoping, Zhang Fuchang, Li Junlin, Zhang Kejin, Gao Xiaoc
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population.
Human genomics 2020 Sep 14 (1): 28.
Tsang Mandy H Y, Kwong Anna K Y, Chan Kate L S, Fung Jasmine L F, Yu Mullin H C, Mak Christopher C Y, Yeung Kit-San, Rodenburg Richard J T, Smeitink Jan A M, Chan Rachel, Tsoi Thomas, Hui Joannie, Wong Shelia S N, Tai Shuk-Mui, Chan Victor C M, Ma Che-Kwan, Fung Sharon T H, Wu Shun-Ping, Chak W K, Chung Brian H Y, Fung Cheuk-Wi
Determining the best candidates for next-generation sequencing-based gene panel for evaluation of early-onset epilepsy.
Molecular genetics & genomic medicine 2020 7 8 (9): e1376.
Lee Jiwon, Lee Chung, Ki Chang-Seok, Lee Jeeh
Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability.
Molecular neurobiology 2023 4 .
Mirgul Bayanova, Aidos K Bolatov, Assiya Bazenova, Lyazzat Nazarova, Alissa Nauryzbayeva, Naanlep Matthew Tanko, Saule Rakhimova, Nazerke Satvaldina, Diana Samakyzy, Ulan Kozhamkulov, Ulykbek Kairov, Ainur Akilzhanova, Dos Sarbass
Investigation of patients with childhood epilepsy in single center: Comprehensive genetic testing experience.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2024 7 .
Hamide Betul Gerik-Celebi, ?pek Dokurel Çetin, Hilmi Bolat, Gul Unsel-Bol
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