Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma

Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma

Saved in:

書目詳細資料
Main Authors:	Piranit Nik Kantaputra, Worrachet Intachai, Bruce M. Carlson, Chulabhorn Pruksachatkunakorn
格式:	雜誌
出版:	2020
主題:	Medicine
在線閱讀:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85078657901&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/68480
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

Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma
由: Piranit Kantaputra, et al.
出版: (2020)

Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findings
由: Kantaputra PN., et al.
出版: (2014)

Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24
由: Martinez-Mir, 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)

TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
由: Piranit Nik Kantaputra, et al.
出版: (2020)

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

Proteomics of hair: effects of pH on the hair shaft
由: Wu, Alicia Rosabee Yu Ling
出版: (2023)

Identification of antibacterial components in human hair shafts
由: Subbaiah, Roopa S., et al.
出版: (2018)

Mutilating keratoderma of Vohwinkel: Successful treatment with etretinate
由: A. Sivayathorn, et al.
出版: (2018)

Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes
由: Piranit Nik Kantaputra, et al.
出版: (2020)

Bacteria display differential growth and adhesion characteristics on human hair shafts
由: Kerk, Swat Kim, et al.
出版: (2018)

Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation
由: Kantaputra P.N., et al.
出版: (2014)

WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts
由: Piranit Nik Kantaputra, et al.
出版: (2019)

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome
由: Piranit Kantaputra, et al.
出版: (2022)

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and aCOL1A2mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

Split hand-foot malformation and a novel WNT10B mutation
由: Piranit Nik Kantaputra, et al.
出版: (2018)

A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: Report of a Thai family
由: Kantaputra P.N., et al.
出版: (2014)

Genetic regulatory pathways of split-hand/foot malformation
由: Piranit N. Kantaputra, et al.
出版: (2018)

Facile and efficient enzymatic methods for harvesting or removal of cuticle cells from human hair shafts
由: Zhang, Nan, et al.
出版: (2022)

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)

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

Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190] [4] (multiple letters)
由: Judith G. Hall, et al.
出版: (2018)

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

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

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)

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

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)

TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly
由: Arunee Kaewkhampa, 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)

Design of shaftings
由: Guerra, Nicanor M.
出版: (1956)

Clinical assessment of absence of the palmaris longus and its association with other anatomical anomalies - A Chinese population study
由: Sebastin, S.J., et al.
出版: (2016)

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

Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations
由: Onnida Wattanarat, et al.
出版: (2018)

Syndromes with supernumerary teeth
由: Mark Lubinsky, et al.
出版: (2018)