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Browsing by Author Chumpol Ngamphiw
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Showing results 1 to 10 of 10
Issue Date
Title
Author(s)
1-Apr-2019
ADAMTSL1 and mandibular prognathism
Piranit N. Kantaputra
;
Apitchaya Pruksametanan
;
Nattapol Phondee
;
Athiwat Hutsadaloi
;
Worrachet Intachai
;
Katsushig Kawasaki
;
Atsushi Ohazama
;
Chumpol Ngamphiw
;
Sissades Tongsima
;
James R. Ketudat Cairns
;
Polbhat Tripuwabhrut
1-Jan-2020
Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --<sup>SEA</sup>/--<sup>CR</sup>, a novel α<sup>0</sup>-thalassemia deletion
Chedtapak Ruengdit
;
Sitthichai Panyasai
;
Naowarat Kunyanone
;
Worawich Phornsiricharoenphant
;
Chumpol Ngamphiw
;
Sissades Tongsima
;
Orapan Sripichai
;
Serge Pissard
;
Sakorn Pornprasert
1-Feb-2022
Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation
Piranit Nik Kantaputra
;
Nutsuchar Wangtiraumnuay
;
Chumpol Ngamphiw
;
Bjorn Olsen
;
Worrachet Intachai
;
Abigail S. Tucker
;
Sissades Tongsima
1-Jan-2022
Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome
Piranit Kantaputra
;
Yeliz Guven
;
Tugba Kalayci
;
Pelin Karaca Özer
;
Wannakamon Panyarak
;
Worrachet Intachai
;
Bjorn Olsen
;
Bruce M. Carlson
;
Oranud Praditsap
;
Sissades Tongsima
;
Chumpol Ngamphiw
;
Peeranat Jatooratthawichot
;
Abigail S. Tucker
;
James R. Ketudat Cairns
1-Jan-2018
Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation
Piranit Nik Kantaputra
;
Wannapa Chinadet
;
Worrachet Intachai
;
Chumpol Ngamphiw
;
James R. Ketudat Cairns
;
Sissades Tongsima
1-Nov-2020
Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2
Piranit Nik Kantaputra
;
Prapai Dejkhamron
;
Sissades Tongsima
;
Chumpol Ngamphiw
;
Worrachet Intachai
;
Lukana Ngiwsara
;
Phannee Sawangareetrakul
;
Jisnuson Svasti
;
Bjorn Olsen
;
James R.Ketudat Cairns
;
Kanokkan Bumroongkit
11-Dec-2009
Mapping human genetic diversity in Asia
Mahmood Ameen Abdulla
;
Ikhlak Ahmed
;
Anunchai Assawamakin
;
Jong Bhak
;
Samir K. Brahmachari
;
Gayvelline C. Calacal
;
Amit Chaurasia
;
Chien Hsiun Chen
;
Jieming Chen
;
Yuan Tsong Chen
;
Jiayou Chu
;
Eva Maria C. Cutiongco-de La Paz
;
Maria Corazon A. De Ungria
;
Frederick C. Delfin
;
Juli Edo
;
Suthat Fuchareon
;
Ho Ghang
;
Takashi Gojobori
;
Junsong Han
;
Sheng Feng Ho
;
Boon Peng Hoh
;
Wei Huang
;
Hidetoshi Inoko
;
Pankaj Jha
;
Timothy A. Jinam
;
Li Jin
;
Jongsun Jung
;
Daoroong Kangwanpong
;
Jatupol Kampuansai
;
Giulia C. Kennedy
;
Preeti Khurana
;
Hyung Lae Kim
;
Kwangjoong Kim
;
Sangsoo Kim
;
Woo Yeon Kim
;
Kuchan Kimm
;
Ryosuke Kimura
;
Tomohiro Koike
;
Supasak Kulawonganunchai
;
Vikrant Kumar
;
Poh San Lai
;
Jong Young Lee
;
Sunghoon Lee
;
Edison T. Liu
;
Partha P. Majumder
;
Kiran Kumar Mandapati
;
Sangkot Marzuki
;
Wayne Mitchell
;
Mitali Mukerji
;
Kenji Naritomi
;
Chumpol Ngamphiw
;
Norio Niikawa
;
Nao Nishida
;
Bermseok Oh
;
Sangho Oh
;
Jun Ohashi
;
Akira Oka
;
Rick Ong
;
Carmencita D. Padilla
;
Prasit Palittapongarnpim
;
Henry B. Perdigon
;
Maude Elvira Phipps
;
Eileen Png
;
Yoshiyuki Sakaki
;
Jazelyn M. Salvador
;
Yuliana Sandraling
;
Vinod Scaria
;
Mark Seielstad
;
Mohd Ros Sidek
;
Amit Sinha
;
Metawee Srikummool
;
Herawati Sudoyo
;
Sumio Sugano
;
Helena Suryadi
;
Yoshiyuki Suzuki
;
Kristina A. Tabbada
;
Adrian Tan
;
Katsushi Tokunaga
;
Sissades Tongsima
;
Lilian P. Villamor
;
Eric Wang
;
Ying Wang
;
Haifeng Wang
;
Jer Yuarn Wu
;
Huasheng Xiao
;
Shuhua Xu
;
Jin Ok Yang
;
Yin Yao Shugart
;
Hyang Sook Yoo
;
Wentao Yuan
;
Guoping Zhao
;
Bin Alwi Zilfalil
1-Jan-2022
Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites
Piranit Kantaputra
;
Peeranat Jatooratthawichot
;
Oranuch Tantachamroon
;
Kamonporn Nanekrungsan
;
Worrachet Intachai
;
Bjorn Olsen
;
Sissades Tongsima
;
Chumpol Ngamphiw
;
James R.Ketudat Cairns
1-Jul-2018
Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation
Piranit Nik Kantaputra
;
Yuddhasert Sirirungruangsarn
;
Worrachet Intachai
;
Chumpol Ngamphiw
;
Sissades Tongsima
;
Prapai Dejkhamron
1-Sep-2020
Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes
Piranit Nik Kantaputra
;
Kanich Tripuwabhrut
;
Worrachet Intachai
;
Bruce M. Carlson
;
Natalina Quarto
;
Chumpol Ngamphiw
;
Sissades Tongsima
;
Nuntigar Sonsuwan