Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation

Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation

Saved in:

書目詳細資料
Main Authors:	Piranit Nik Kantaputra, Chotika Bongkochwilawan, Massupa Kaewgahya, Atsushi Ohazama, Hulya Kayserili, Arzu Pinar Erdem, Oya Aktoren, Yeliz Guven
格式:	雜誌
出版:	2018
在線閱讀:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84904409608&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45769
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!
機構:	Chiang Mai University

相似書籍

Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation
由: Kantaputra P.N., et al.
出版: (2014)

Enamel-renal-gingival syndrome and FAM20A mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Enamel-renal-gingival syndrome and FAM20A mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Enamel-renal-gingival syndrome and FAM20A mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Periodontal disease and FAM20A mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Periodontal disease and FAM20A mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation
由: Yeliz Guven, et al.
出版: (2018)

Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation
由: Yeliz Guven, et al.
出版: (2018)

Enamel-renal-gingival syndrome and FAM20A mutations
由: Kantaputra P.N., et al.
出版: (2014)

Enamel-renal-gingival syndrome and FAM20A mutations
由: Kantaputra P.N., et al.
出版: (2014)

All enamel is not created equal: Supports from a novel FAM83H mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

WNT10A and isolated hypodontia
由: Piranit Kantaputra, et al.
出版: (2018)

Periodontal disease and FAM20A mutations
由: Kantaputra P., et al.
出版: (2017)

Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patient
由: Hülya Kayserili, et al.
出版: (2018)

All enamel is not created equal: Supports from a novel FAM83H mutation
由: Kantaputra P., et al.
出版: (2017)

Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI
由: Piranit Nik Kantaputra, et al.
出版: (2018)

WNT10A and isolated hypodontia
由: Kantaputra P., et al.
出版: (2017)

TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
由: Arunee Kaewkhampa, et al.
出版: (2018)

Root dentin anomaly and a PLG mutation
由: Napaporn Tananuvat, et al.
出版: (2018)

Root dentin anomaly and a PLG mutation
由: Napaporn Tananuvat, et al.
出版: (2018)

Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations
由: Piranit Nik Kantaputra, et al.
出版: (2018)

TFAP2B mutation and dental anomalies
由: Natchaya Tanasubsinn, et al.
出版: (2018)

Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

TFAP2B mutation and dental anomalies
由: Natchaya Tanasubsinn, et al.
出版: (2018)

TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
由: Kaewkhampa A., et al.
出版: (2014)

Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Hypodontia With Class I Malloclusion and Maxillary Diastema
由: Bunga Fatimah, et al.
出版: (2018)

Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations
由: P. N. Kantaputra, et al.
出版: (2018)

Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations
由: Kantaputra P.N., et al.
出版: (2014)

Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations
由: P. N. Kantaputra, et al.
出版: (2018)

Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Severe hypodontia and oral xanthomas in Alagille syndrome [1]
由: Ho, N.C., et al.
出版: (2013)

Fam (ily)
由: Lim, Diane Yan Tong
出版: (2019)

BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells
由: Piranit Nik Kantaputra
出版: (2018)

Response to the Letter to the Editor by Idil Kurtulus-Waschulewski; Gerhard Wahl, Prof. Dr.; Katalyn Dittrich; Volker Schuster
由: Piranit Nik Kantaputra
出版: (2018)

Clinical Correlate: CLCN7-Associated Autosomal Recessive Osteopetrosis
由: Piranit Nik Kantaputra
出版: (2018)