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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 25, 2023. (Total: 221440Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Mental Retardation and MTHFR[original query]
Molecular and clinical characterisation of homocystinuria in two Austrian families with cystathionine beta-synthase deficiency.
Acta medica Austriaca 2002 1 28 (5): 145-51.
Tröndle U, Sunder-Plassmann G, Burgmann H, Buchmayer H, Kramer L, Bieglmayer C, Hörl W H, Födinger
Infant C677T MTHFR polymorphism and severe mental retardation.
Birth defects research. Part A, Clinical and molecular teratology 2007 Jan 79 (1): 24-6.
Shaw Gary M, Jelliffe-Pawlowski Laura, Nelson Verne, Zhu Huiping, Harris John A, Finnell Richard
Screening for methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Indian patients with idiopathic mental retardation.
Nutritional neuroscience 2008 Feb 11 (1): 18-24.
Dutta Samikshan, Das Bhowmik Aneek, Sinha Swagata, Chattopadhyay Anindita, Mukhopadhyay Kanch
Methylenetetrahydrofolate reductase gene polymorphisms and cerebral palsy in Chinese infants.
Journal of human genetics 2011 Jan 56 (1): 17-21.
Cheng Xiuyong, Li Tongchuan, Wang Honglian, Zhu Dengna, Ma Caiyun, Ma Bingxiang, Wang Yinghong, Zhang Junyu, Guo Luo, Wang Lei, Yun Liu, Chen Shiting, Jiang Zedong, He Lin, Zhu Changlian, Xing Qing
Methylenetetrahydrofolate reductase polymorphism is not risk factor for Down syndrome in North India.
Indian journal of human genetics 2014 Apr 20 (2): 142-7.
Rai Vandana, Yadav Upendra, Kumar Pradeep, Yadav Sushil Kum
Maternal germline factors associated with aneuploid pregnancy loss: a systematic review.
Human reproduction update 2021 .
Blyth Ursula, Craciunas Laurentiu, Hudson Gavin, Choudhary Meenaks
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