Compound Heterozygosity for a Novel Frameshift Variant Causing Fatal Infantile Liver Failure and Genotype–Phenotype Correlation of <i>POLG</i> c.3286C>T Variant by Kanokwan Sriwattanapong, Kitiwan Rojnueangnit, Thanakorn Theerapanon, Chalurmpon Srichomthong, Thantrira Porntaveetus, Vorasuk Shotelersuk

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Whole genome and exome sequencing of monozygotic twins with trisomy 21, discordant for a congenital heart defect and epilepsy. by Pongsathorn Chaiyasap, Supasak Kulawonganunchai, Chalurmpon Srichomthong, Sissades Tongsima, Kanya Suphapeetiporn, Vorasuk Shotelersuk

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Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis by Suramath Isaranuwatchai, Ankanee Chanakul, Chupong Ittiwut, Rungnapa Ittiwut, Chalurmpon Srichomthong, Vorasuk Shotelersuk, Kanya Suphapeetiporn, Kearkiat Praditpornsilpa

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Genome of Varanus salvator macromaculatus (Asian Water Monitor) Reveals Adaptations in the Blood Coagulation and Innate Immune System by Wanna Chetruengchai, Wanna Chetruengchai, Wanna Chetruengchai, Worapong Singchat, Worapong Singchat, Chalurmpon Srichomthong, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Adjima Assawapitaksakul, Kornsorn Srikulnath, Kornsorn Srikulnath, Syed Farhan Ahmad, Syed Farhan Ahmad, Chureerat Phokaew, Chureerat Phokaew, Chureerat Phokaew, Vorasuk Shotelersuk, Vorasuk Shotelersuk

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A patient with combined pituitary hormone deficiency and osteogenesis imperfecta associated with mutations in LHX4 and COL1A2 by Nalinee Hemwong, Chureerat Phokaew, Chalurmpon Srichomthong, Siraprapa Tongkobpetch, Khomsak Srilanchakon, Vichit Supornsilchai, Kanya Suphapeetiporn, Thantrira Porntaveetus, Vorasuk Shotelersuk

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HLA-B*46:01:01:01 and HLA-DRB1*09:01:02:01 are associated with anti-rHuEPO-induced pure red cell aplasia by Thitima Benjachat Suttichet, Monpat Chamnanphon, Monnat Pongpanich, Sarun Chokyakorn, Pawinee Kupatawintu, Chalurmpon Srichomthong, Wanna Chetruengchai, Hathaichanok Chuntakaruk, Thanyada Rungrotmongkol, Pajaree Chariyavilaskul, Vorasuk Shotelersuk, Kearkiat Praditpornsilpa

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A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases by Thivaratana Sinthuwiwat, Supranee Buranapraditkun, Wuttichart Kamolvisit, Siraprapa Tongkobpetch, Wanna Chetruengchai, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Chureerat Phokaew, Patipark Kueanjinda, Tanapat Palaga, Tadech Boonpiyathad, Kanya Suphapeetiporn, Nattiya Hirankarn, Vorasuk Shotelersuk

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Comparative genomics and genome-wide SNPs of endangered Eld’s deer provide breeder selection for inbreeding avoidance by Vichayanee Pumpitakkul, Wanna Chetruengchai, Chalurmpon Srichomthong, Chureerat Phokaew, Wirulda Pootakham, Chutima Sonthirod, Wanapinun Nawae, Sissades Tongsima, Pongsakorn Wangkumhang, Alisa Wilantho, Yongchai Utara, Ampika Thongpakdee, Saowaphang Sanannu, Umaporn Maikaew, Suphattharaphonnaphan Khuntawee, Wirongrong Changpetch, Phairot Phromwat, Kacharin Raschasin, Phunyaphat Sarnkhaeveerakul, Pannawat Supapannachart, Wannapol Buthasane, Budhan S. Pukazhenthi, Klaus-Peter Koepfli, Prapat Suriyaphol, Sithichoke Tangphatsornruang, Gunnaporn Suriyaphol, Vorasuk Shotelersuk

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