SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis

by Kantaputra P.
Published 2023

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome

by Kantaputra P.
Published 2023

CACNA1S mutation-associated dental anomalies: A calcium channelopathy

by Kantaputra P.
Published 2023

Laurin-Sandrow syndrome with additional associated manifestations

by Kantaputra P.N.
Published 2014

Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings

by Kantaputra P.N.
Published 2014

Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al.

by Kantaputra P.N.
Published 2014

BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells

by Kantaputra P.N.
Published 2014

Dentinogenesis imperfecta-associated syndromes

by Kantaputra P.N.
Published 2014

WNT10A and isolated hypodontia

by Kantaputra P., Sripathomsawat W.
Published 2017

Syndromes with supernumerary teeth

by Lubinsky M., Kantaputra P.
Published 2017

Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations

by Wattanarat O., Kantaputra P.
Published 2017

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

Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patient

by Kayserili H., Kantaputra P.N.
Published 2014

A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth

by Kantaputra P.N., Mai C.
Published 2014

A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome

by Kantaputra P.N., Mundlos S., Sripathomsawat W.
Published 2014

WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity

by Kantaputra P., Kaewgahya M., Kantaputra W.
Published 2014

All enamel is not created equal: Supports from a novel FAM83H mutation

by Kantaputra P., Intachai W., Auychai P.
Published 2017