Human asparagine synthetase associates with the mitotic spindle

由 Chalongrat Noree, Elena Monfort, Vorasuk Shotelersuk
出版 2019

Human asparagine synthetase associates with the mitotic spindle

由 Chalongrat Noree, Monfort, Elena, Vorasuk Shotelersuk
出版 2018

A somatic pik3ca p.h1047l mutation in a Thai patient with isolated macrodactyly: A case report

由 Wandee Udomchaiprasertkul, Pravit Kitidumrongsook, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2020

Double heterozygous variants in FBN1 and FBN2 in a Thai woman with Marfan and Beals syndromes

由 Chureerat Phokaew, Rekwan Sittiwangkul, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2020

Short stature, platyspondyly, hip dysplasia, and retinal detachment: An atypical type II collagenopathy caused by a novel mutation in the C-propeptide region of COL2A1: A case repo...

由 Apiruk Sangsin, Chalurmpon Srichomthong, Monnat Pongpanich, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

Two novel EBP mutations in Conradi-Hünermann-Happle syndrome

由 Surasawadee Ausavarat, Pranoot Tanpaiboon, Siraprapa Tongkobpetch, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

Precision medicine in Thailand

由 Vorasuk Shotelersuk, Sissades Tongsima, Manop Pithukpakorn, Jakris Eu-ahsunthornwattana, Surakameth Mahasirimongkol
出版 2020

Cystinuria: Cause of recurrent renal stones in a 4-year-old girl

由 Kanchana Tangnararatchakit, Watcharin Ariyaprakai, Wiwat Tapaneya-Olarn, Vorasuk Shotelersuk, Thanom Petchthong
出版 2018

The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: A case report

由 Chulaluck Kuptanon, Chalurmpon Srichomthong, Apiruk Sangsin, Dool Kovitvanitcha, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

Two novel compound heterozygous BMP1 mutations in a patient with osteogenesis imperfecta: A case report

由 Apiruk Sangsin, Chulaluck Kuptanon, Chalurmpon Srichomthong, Monnat Pongpanich, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

A novel de novo COL1A1 mutation in a thai boy with osteogenesis im perfecta born to consanguineous parents

由 Siraprapa Tongkobpetch, Noppachart Limpaphayom, Apiruk Sangsin, Thantrira Porntaveetus, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand

由 Pongsathorn Chaiyasap, Chupong Ittiwut, Chalurmpon Srichomthong, Apiruk Sangsin, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

Two novel compound heterozygous BMP1 mutations in a patient with osteogenesis imperfecta: A case report

由 Apiruk Sangsin, Chulaluck Kuptanon, Chalurmpon Srichomthong, Monnat Pongpanich, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand

由 Pongsathorn Chaiyasap, Chupong Ittiwut, Chalurmpon Srichomthong, Apiruk Sangsin, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

A novel de novo COL1A1 mutation in a thai boy with osteogenesis im perfecta born to consanguineous parents

由 Siraprapa Tongkobpetch, Noppachart Limpaphayom, Apiruk Sangsin, Thantrira Porntaveetus, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

The most 5′ truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report

由 Chulaluck Kuptanon, Chalurmpon Srichomthong, Apiruk Sangsin, Dool Kovitvanitcha, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018

A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome

由 Prapai Dejkhamron, Chupong Ittiwut, Hataitip Tangngam, Kanokkarn Sunkonkit, Rungrote Natesirinilkul, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2019

Dosage Optimization of Efavirenz Based on a Population Pharmacokinetic–Pharmacogenetic Model of HIV-infected Patients in Thailand

由 Piyawat Chaivichacharn, Anchalee Avihingsanon, Weerawat Manosuthi, Sasiwimol Ubolyam, Siraprapa Tongkobpetch, Vorasuk Shotelersuk, Baralee Punyawudho
出版 2020

Discrepancy in the degree of polycythemia in a family with a novel nonsense EPOR mutation

由 Chitsanupong Ratarat, Chupong Ittiwut, Rungrote Natesirinilkul, Lalita Sathitsamitpong, Kanda Fanhchaksai, Pimlak Charoenkwan, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2019

A common and two novel GBA mutations in Thai patients with Gaucher disease

由 Rachaneekorn Tammachote, Siraprapa Tongkobpetch, Chalurmpon Srichomthong, Kampon Phipatthanananti, Suthipong Pungkanon, Duangrurdee Wattanasirichaigoon, Kanya Suphapeetiporn, Vorasuk Shotelersuk
出版 2018