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Results 1-10 of 23 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1-Jan-2013
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases
Piranit Nik Kantaputra
;
Rekwan Sittiwangkul
;
Nuntigar Sonsuwan
;
Valeria Romanelli
;
Jair Tenorio
;
Pablo Lapunzina
1-Jan-2014
Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation
Yeliz Guven
;
Umut Altunoglu
;
Oya Aktoren
;
Zehra Oya Uyguner
;
Hulya Kayserili
;
Massupa Kaewkahya
;
Piranit Nik Kantaputra
1-Jan-2014
Root dentin anomaly and a PLG mutation
Napaporn Tananuvat
;
Pimlak Charoenkwan
;
Atsushi Ohazama
;
James R. Ketuda Cairns
;
Massupa Kaewgahya
;
Piranit Nik Kantaputra
1-Jan-2014
Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation
Piranit Nik Kantaputra
;
Chotika Bongkochwilawan
;
Massupa Kaewgahya
;
Atsushi Ohazama
;
Hulya Kayserili
;
Arzu Pinar Erdem
;
Oya Aktoren
;
Yeliz Guven
1-Jan-2014
Enamel-renal-gingival syndrome and FAM20A mutations
Piranit Nik Kantaputra
;
Massupa Kaewgahya
;
Udomrat Khemaleelakul
;
Prapai Dejkhamron
;
Suchitra Sutthimethakorn
;
Visith Thongboonkerd
;
Anak Iamaroon
1-Jan-2014
BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells
Piranit Nik Kantaputra
1-Jan-2014
Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations
Piranit Nik Kantaputra
;
Hulya Kayserili
;
Yeliz Guven
;
Warissara Kantaputra
;
Mehmet C. Balci
;
Pranoot Tanpaiboon
;
Napaporn Tananuvat
;
Anusha Uttarilli
;
Ashwin Dalal
1-Jan-2014
Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI
Piranit Nik Kantaputra
;
Hülya Kayserili
;
Yeliz Güven
;
Warissara Kantaputra
;
Mehmet C. Balci
;
Pranoot Tanpaiboon
;
Anusha Uttarilli
;
Ashwin Dalal
1-Sep-2012
Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation
Piranit Nik Kantaputra
;
Wannapa Chinadet
;
Atsushi Ohazama
;
Michihiro Kono
1-Jul-2012
Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation
Piranit Nik Kantaputra
;
Ans van den Ouweland
;
Tumtip Sangruchi
;
Chanin Limwongse
Discover
Author
6
Massupa Kaewgahya
5
Atsushi Ohazama
5
Worrachet Intachai
4
James R. Ketudat Cairns
4
Yeliz Guven
3
Hulya Kayserili
3
Mark Lubinsky
3
Prapai Dejkhamron
2
Anusha Uttarilli
2
Ashwin Dalal
.
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