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Cancer Genetics and Cytogenetics|October 11, 2005
Mutations of the FLT3 gene in adult acute myeloid leukemia: determination of incidence and identification of a novel mutation in a Thai populationChirayu U Auewarakul, Narongrit Sritana, Chanin Limwongse, et al.
Case Reports in Dermatology|September 10, 2015
Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis CongenitaBenjaporn Panichareon, Thanawat Seedapan, Wanna Thongnoppakhun, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5Piranit N Kantaputra, Yupada Pongprot, Oranud Praditsap, et al.
Case Reports in Neurology|April 8, 2014
A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with InflammationJantima Tanboon, Kanjana Rongsa, Manop Pithukpakorn, et al.
Plos Neglected Tropical Diseases|August 4, 2012
Activation of indoleamine 2,3-dioxygenase in patients with scrub typhus and its role in growth restriction of Orientia tsutsugamushiThanavadee Prachason, Kanittha Konhan, Piyapat Pongnarin, et al.
BMC Bioinformatics|September 19, 2009
Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analysesWaranyu Wongseree, Anunchai Assawamakin, Theera Piroonratana, et al.
Molecular Genetics & Genomic Medicine|May 31, 2021
Identification of novel mutation in RANKL by whole-exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosisPongtawat Lertwilaiwittaya, Bhoom Suktitipat, Phongphak Khongthon, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|October 7, 2023
Familial clustering of nonalcoholic fatty liver disease in first-degree relatives of adults with lean nonalcoholic fatty liver diseaseSorachat Niltwat, Chanin Limwongse, Natthinee Charatcharoenwitthaya, et al.
Molecular Vision|June 3, 2011
Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridiaShagun Aggarwal, Worapoj Jinda, Chanin Limwongse, et al.
International Ophthalmology|September 2, 2020
Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genesWorapoj Jinda, Aekkachai Tuekprakhon, Wanna Thongnoppakhun, et al.
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