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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 30, 2023. (Total: 223474Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Abnormalities and ALPL[original query]
Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine Disorders.
The Journal of clinical endocrinology and metabolism 2018 4 103 (6): 2234-2243.
Dahir Kathryn M, Tilden Daniel R, Warner Jeremy L, Bastarache Lisa, Smith Derek K, Gifford Aliya, Ramirez Andrea H, Simmons Jill S, Black Margo M, Newman John H, Denny Josh
Epidemiological, Clinical and Genetic Study of Hypophosphatasia in A Spanish Population: Identification of Two Novel Mutations in The Alpl Gene.
Scientific reports 2019 7 9 (1): 9569.
García-Fontana Cristina, Villa-Suárez Juan M, Andújar-Vera Francisco, González-Salvatierra Sheila, Martínez-Navajas Gonzalo, Real Pedro J, Gómez Vida José M, de Haro Tomás, García-Fontana Beatriz, Muñoz-Torres Manu
Gene coexpression network analysis revealed biomarkers correlated with blast cells and survival in acute myeloid leukemia.
Molecular and clinical oncology 2020 4 12 (5): 475-484.
Pan Yuming, Zhang Qiaoxia, Deng Xiaopeng, An Na, Du Xin, Liu Jiaj
Genetic polymorphisms in CLDN14 (rs219780) and ALP (rs1256328) genes are associated with risk of nephrolithiasis in Egyptian children.
Turkish journal of urology 2020 Oct .
Elshamaa Manal F, Fadel Fatina I, Kamel Soal, Farouk Hebatallah, Alahmady Mostafa, Ramadan Yas
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