P. Siriwan

发表

De novo missense mutation, S541Y, in the p63 gene underlying Rapp–Hodgkin ectodermal dysplasia syndrome

V. Shotelersuk, S. Tongkobpetch, S. Janklat, 2005, Clinical and experimental dermatology.

A mutation of the p63 gene in non-syndromic cleft lip

V. Shotelersuk, P. Leoyklang, P. Siriwan, 2006, Journal of Medical Genetics.

A Novel Mutation in EFNB1, Probably with a Dominant Negative Effect, Underlying Craniofrontonasal Syndrome

V. Shotelersuk, P. Siriwan, Surasawadee Ausavarat, 2006, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

PDGFRa mutations in humans with isolated cleft palate

C. Srichomthong, K. Suphapeetiporn, V. Shotelersuk, 2012, European Journal of Human Genetics.

Significant association between IRF6 820G→A and non-syndromic cleft lip with or without cleft palate in the Thai population

C. Srichomthong, V. Shotelersuk, P. Siriwan, 2005, Journal of Medical Genetics.

Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome

K. Suphapeetiporn, V. Shotelersuk, P. Siriwan, 2009, American journal of medical genetics. Part A.

Variants of the CDH1 (E-Cadherin) Gene Associated with Oral Clefts in the Thai Population.

K. Suphapeetiporn, V. Shotelersuk, C. Ittiwut, 2016, Genetic testing and molecular biomarkers.

Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele.

K. Suphapeetiporn, V. Shotelersuk, P. Siriwan, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Epidemiology of cleft lip with or without cleft palate in Thais

K. Suphapeetiporn, V. Shotelersuk, R. Ittiwut, 2017 .

The role of SMAS flap in preventing Frey's syndrome following standard superficial parotidectomy.

P. Siriwan, A. Angspatt, P. Chokrungvaranont, 2004, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects

Tayard Desudchit, Vorasuk Shotelersuk, W. Gahl, 2007, Human mutation.

TBX22 mutations are a frequent cause of non‐syndromic cleft palate in the Thai population

K. Suphapeetiporn, V. Shotelersuk, S. Tongkobpetch, 2007, Clinical genetics.

Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip

V. Shotelersuk, C. Ittiwut, P. Siriwan, 2003, Journal of medical genetics.

Bilateral scrotal flaps: a skin restoration for penile paraffinoma.

P. Siriwan, A. Angspatt, P. Chokrungvaranont, 2005, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Prevalence and characteristics of congenital hand and foot anomalies requiring surgery in remote areas of Thailand

S. Honsawek, P. Siriwan, P. Kitidumrongsook, 2017 .

Normal Palatal Sutures in Newborns and Fetuses: A Critical Fact for Successful Palatal Distraction

T. Tansatit, P. Siriwan, N. Rojvachiranonda, 2003, The Journal of craniofacial surgery.

Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.

K. Suphapeetiporn, S. Tongkobpetch, P. Siriwan, 2008, International journal of oral and maxillofacial surgery.

MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population

V. Shotelersuk, S. Tongkobpetch, P. Siriwan, 2006, Journal of Human Genetics.

Cadaveric Study of the Nasal Periosteum and Implant Position After Augmentation Rhinoplasty

P. Siriwan, N. Rojvachiranonda, C. Mahatumarat, 2012, The Journal of craniofacial surgery.

Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.

K. Suphapeetiporn, V. Shotelersuk, S. Tongkobpetch, 2008, International journal of oral and maxillofacial surgery.

FOXE1 mutations in Thai patients with oral clefts.

C. Srichomthong, K. Suphapeetiporn, V. Shotelersuk, 2013, Genetics research.