Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: TRNT1[original query] |
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Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Human molecular genetics 2017 Mar 26 (6): 1193-1204. Jain Deepti, Hodonsky Chani J, Schick Ursula M, Morrison Jean V, Minnerath Sharon, Brown Lisa, Schurmann Claudia, Liu Yongmei, Auer Paul L, Laurie Cecelia A, Taylor Kent D, Browning Brian L, Papanicolaou George, Browning Sharon R, Loos Ruth J F, North Kari E, Thyagarajan Bharat, Laurie Cathy C, Thornton Timothy A, Sofer Tamar, Reiner Alexander |
Genotype/phenotype correlations of childhood-onset congenital sideroblastic anaemia in a European cohort. British journal of haematology 2019 7 187 (4): 530-542. Fouquet Cyrielle, Le Rouzic Marie-Amelyne, Leblanc Thierry, Fouyssac Fanny, Leverger Guy, Hessissen Laila, Marlin Sandrine, Bourrat Emmanuelle, Fahd Mony, Raffoux Emmanuel, Vannier Jean-Pierre, Jäkel Nadja, Knoefler Ralf, Triolo Valerie, Pasquet Marlene, Bayart Sophie, Thuret Isabelle, Lutz Patrick, Vermylen Christiane, Touati Mohamed, Rose Christian, Matthes Thomas, Isidor Bertrand, Kannengiesser Caroline, Ducassou Stepha |
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). Scientific reports 2021 Apr 11 (1): 8308. Bisgin Atil, Sonmezler Ozge, Boga Ibrahim, Yilmaz Musta |
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Journal of neurology 2021 1 268 (6): 2192-2207. Chakrabarty Sanjiban, Govindaraj Periyasamy, Sankaran Bindu Parayil, Nagappa Madhu, Kabekkodu Shama Prasada, Jayaram Pradyumna, Mallya Sandeep, Deepha Sekar, Ponmalar J N Jessiena, Arivinda Hanumanthapura R, Meena Angamuthu Kanikannan, Jha Rajan Kumar, Sinha Sanjib, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasamy, Satyamoorthy Kapaet |
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