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

[1]  K. Suphapeetiporn,et al.  TBX22 mutations are a frequent cause of non‐syndromic cleft palate in the Thai population , 2007, Clinical genetics.

[2]  K. Christensen,et al.  PVRL1 variants contribute to non‐syndromic cleft lip and palate in multiple populations , 2006, American journal of medical genetics. Part A.

[3]  V. Shotelersuk,et al.  MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population , 2006, Journal of Human Genetics.

[4]  V. Shotelersuk,et al.  A mutation of the p63 gene in non-syndromic cleft lip , 2006, Journal of Medical Genetics.

[5]  A. Palmieri,et al.  Study of the PVRL1 Gene in Italian Nonsyndromic Cleft Lip Patients with or without Cleft Palate , 2006, Annals of human genetics.

[6]  H. Hsiao,et al.  A study of PVRL1 mutations for non-syndromic cleft lip and/or palate among Taiwanese patients. , 2006, International journal of oral and maxillofacial surgery.

[7]  C. Srichomthong,et al.  Significant association between IRF6 820G→A and non-syndromic cleft lip with or without cleft palate in the Thai population , 2005, Journal of Medical Genetics.

[8]  V. Shotelersuk,et al.  De novo missense mutation, S541Y, in the p63 gene underlying Rapp–Hodgkin ectodermal dysplasia syndrome , 2005, Clinical and experimental dermatology.

[9]  A. Palmieri,et al.  Investigation of the W185X nonsense mutation of PVRL1 gene in Italian nonsyndromic cleft lip and palate patients , 2004, American journal of medical genetics. Part A.

[10]  K. Irie,et al.  Nectins and nectin‐like molecules: Roles in cell adhesion, migration, and polarization , 2003, Cancer science.

[11]  V. Shotelersuk,et al.  Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip , 2003, Journal of medical genetics.

[12]  N. Niikawa,et al.  A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome. , 2003, International journal of molecular medicine.

[13]  R. Spritz,et al.  The genetics and epigenetics of orofacial clefts , 2001, Current opinion in pediatrics.

[14]  R. Spritz,et al.  Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela , 2001, Nature Genetics.

[15]  R. Spritz,et al.  Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia , 2000, Nature Genetics.

[16]  F. Beemer,et al.  MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans , 2000, Nature Genetics.

[17]  J. Červenka,et al.  Classification and birth prevalence of orofacial clefts. , 1998, American journal of medical genetics.

[18]  J. Murray,et al.  The many faces and factors of orofacial clefts. , 1999, Human molecular genetics.