Thyroid dysfunction in a patient with aglossia

by Kantaputra P., Tanpaiboon P.
Published 2014

Thyroid dysfunction in a patient with aglossia

by Kantaputra P., Tanpaiboon P.
Published 2014

A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?

by Kantaputra P.N., Tanpaiboon P.
Published 2014

A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?

by Kantaputra P.N., Tanpaiboon P.
Published 2014

Two novel EBP mutations in Conradi-Hünermann-Happle syndrome

by Ausavarat S., Tanpaiboon P., Tongkobpetch S., Suphapeetiporn K., Shotelersuk V.
Published 2014

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)

by Hall J.G., Kantaputra P.N., Tanpaiboon P.
Published 2014

Rapid diagnosis of trisomy 21 by relative gene copy using real-time quantitative polymerase chain reaction

by Sanguansermsri,C., Tanpaiboon,P., Charoenkwan,P., Phusua,A., Sanguansermsri,T.
Published 2015

Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome

by Kantaputra P.N., Tanpaiboon P., Unachak K., Praphanphoj V.
Published 2014

Rapid diagnosis of trisomy 21 by relative gene copy using real-time quantitative polymerase chain reaction

by Sanguansermsri C., Tanpaiboon P., Charoenkwan P., Phusua A., Sanguansermsri T.
Published 2014

Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome

by Kantaputra P.N., Tanpaiboon P., Unachak K., Praphanphoj V.
Published 2014

c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and robin sequence in a Thai patient

by Tanpaiboon,P., Kantaputra,P.N.I., Wejathikul,K., Piyamongkol,W.
Published 2015

Isolated methylmalonic acidemia with unusual presentation mimicking diabetic ketoacidosis

by Dejkhamron P., Wejapikul K., Unachak K., Sawangareetrakul P., Tanpaiboon P., Wattanasirichaigoon D.
Published 2017

Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation

by Tanpaiboon P., Sittiwangkul R., Dejkhamron P., Srikummool M., Sripathomsawat W., Kantaputra P.
Published 2014

Thyroid functions in children with Down's syndrome

by Unachak K., Tanpaiboon P., Pongprot Y., Sittivangkul R., Silvilairat S., Dejkhamron P., Sudasna J.
Published 2014

Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome

by Sripathomsawat W., Tanpaiboon P., Heering J., Dotsch V., Hennekam R.C., Kantaputra P.
Published 2014

The smallest teeth in the world are caused by mutations in the PCNT gene

by Kantaputra P., Tanpaiboon P., Porntaveetus T., Ohazama A., Sharpe P., Rauch A., Hussadaloy A., Thiel C.T.
Published 2014

Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI

by Kantaputra P.N., Kayserili H., Guven Y., Kantaputra W., Balci M.C., Tanpaiboon P., Uttarilli A., Dalal A.
Published 2014

Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations

by Kantaputra P.N., Kayserili H., Guven Y., Kantaputra W., Balci M.C., Tanpaiboon P., Tananuvat N., Uttarilli A., Dalal A.
Published 2014

Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome

by Keeratichamroen S., Ketudat Cairns J.R., Wattanasirichaigoon D., Wasant P., Ngiwsara L., Suwannarat P., Pangkanon S., Kuptanon J., Tanpaiboon P., Rujirawat T., Liammongkolkul S., Svasti J.
Published 2014

Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects

by Kruszka P., Tanpaiboon P., Neas K., Crosby K., Berger S., Martinez A., Addissie Y., Pongprot Y., Sittiwangkul R., Silvilairat S., Makonkawkeyoon K., Yu L., Wynn J., Bennett J., Mefford H., Reynolds W., Liu X., Mommersteeg M., Chung W., Lo C., Muenke M.
Published 2017