• A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts
• A Multivariate Analysis of Unilateral Cleft Lip and Palate Facial Skeletal Morphology
• A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis
• A Rare Case of Cleft Palate Associated With Tongue Hamartoma: A Case Report and Systematic Review
• A retrospective study of congenital anomalies and associated risk factors among children admitted at a tertiary hospital in northwestern Tanzania
• Academic achievement in children with oral clefts versus unaffected siblings
• An Evaluation of Muscle Repair Techniques: Implications in Musculoskeletal Healing and Corollaries in Oral-Facial Clefting
• An overview of cleft lip and palate
• An Overview of Timeline of Interventions in the Continuum of Cleft Lip and Palate Care
• Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with <em>DMD, FGF13, EGFL6</em>, and Additional Loci at Xp22.2
• Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2
• Anterior cleft palate due to Cbfb deficiency and its rescue by folic acid
• Asian oral-facial cleft birth prevalence
• Associated malformations in patients with limb reduction deficiencies
• Association between inhibited binding of folic acid to folate receptor alpha in maternal serum and folate-related birth defects in Norway
• Bilateral cleft lip and palate: A morphometric analysis of facial skeletal form using cone beam computed tomography
• Candidate genes for oral-facial clefts in Guatemalan families
• Ciliopathic micrognathia is caused by aberrant skeletal differentiation and remodeling
• Ciliopathy Protein Tmem107 Plays Multiple Roles in Craniofacial Development
• Cleft lip and palate and related factors: A 10 years study in university hospitalised patients at Mashhad--Iran
• Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia
• Combined anomalies of the palate in Mohr syndrome: is preoperative electromyography of the palate useful?
• Compound heterozygous alterations in intraflagellar transport protein <em>CLUAP1</em> in a child with a novel Joubert and oral-facial-digital overlap syndrome
• Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndrome
• Confirmation that mutations in DDX59 cause an autosomal recessive form of oral-facial-digital syndrome: Further delineation of the DDX59 phenotype in two new families
• Contemporary Prevalence of Oral Clefts in the US: Geographic and Socioeconomic Considerations
• Craniofacial characteristics evidenced in Bartsocas-Papas syndrome from birth to five years. Case report
• Defective sumoylation pathway directs congenital heart disease
• Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI
• Developmental disorders of the dentition: an update
• Disruption of the murine Ap2beta1 gene causes nonsyndromic cleft palate
• Disruption of the murine Ap2β1 gene causes nonsyndromic cleft palate
• Dose-Dependent Antiteratogenic Effects of Folic Acid on All-Trans Retinoic Acid-Induced Cleft Palate in Fetal Mice
• E-cadherin variants associated with oral facial clefts trigger aberrant cell motility in a REG1A-dependent manner
• EFFECT OF BIOPSYCHOSOCIAL INTERVENTION ON BEAUTY SATISFACTION AFTER STAGED SURGERY AMONG ADOLESCENTS WITH ORAL FACIAL CLEFTS
• Effects of Primary Alveolar Grafting on Alveolar Bone Thickness in Patients With Cleft Lip and Palate
• Environmental factors in the first trimester and risk of oral-facial clefts in the offspring
• Epithelial branching morphogenesis of salivary gland: exploration of new functional regulators
• Etiology and genetic factors in clefts of lip and/or palate reported at children's hospital, Lahore, Pakistan
• Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI
• Facial soft-tissue asymmetry in three-dimensional cone-beam computed tomography images of children with surgically corrected unilateral clefts
• Facial tissue depths in children with cleft lip and palate
• Familial recurrence of midline birth defects--a nationwide danish cohort study
• Family-based genome-wide association study in Patagonia confirms the association of the DMD locus and cleft lip and palate
• Fibrocystic disease of liver and pancreas; under-recognized features of the X-linked ciliopathy oral-facial-digital syndrome type 1 (OFD I)
• Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts
• Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders
• Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts
• Homocysteine and folic acid: implications for pregnancy
• Incidence of cleft lip and palate in Uganda
• Interferon regulatory factor 6 (IRF6) is associated with oral-facial cleft in individuals that originate in South America
• Is MTHFD1 polymorphism rs 2236225 (c.1958G&gt;A) associated with the susceptibility of NSCL/P? A systematic review and meta-analysis
• Is there Seasonality in the Incidence of Oral-Facial Clefts?
• Maxillary rehabilitation using a removable partial denture with attachments in a cleft lip and palate patient: a clinical report
• Melatonin inhibits embryonic salivary gland branching morphogenesis by regulating both epithelial cell adhesion and morphology
• Midline Cleft of Lip With Preaxial Polydactyly in One Hand: A Possible New Variation of Thurston Syndrome?
• Molecular, clinical and political approaches to the problem of cleft lip and palate
• Multiple milia in a newborn with congenital malformations: oral-facial-digital syndrome type 1
• Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients
• Nasal airway and septal variation in unilateral and bilateral cleft lip and palate
• Novel Digital Workflow for Nasoalveolar Molding and Postoperative Nasal Stent for Infants With Cleft Lip and Palate
• Novel Surgical Technique for Correction of Incomplete Median Cleft Lip Deformity in Oral-Facial-Digital Syndrome Type II
• Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study
• Oral-facial digital syndrome type 1
• Oral-Facial-Digital Syndrome Type 1: A Case Report and Review
• Oral-Facial-Digital Syndrome Type 1: Further Clinical and Molecular Delineation in 2 New Families
• Oral-facial-digital syndrome type 1: oral features in 12 patients submitted to clinical and radiographic examination
• ORAL-FACIAL-DIGITAL SYNDROME TYPE I (CLINICAL CASE)
• Oral-facial-digital syndrome type I: surgical approach and a case report
• Oral-facial-digital syndrome type I. A case report
• Oral-Facial-Digital Syndrome Type IX with Subfoveal Drusenoid Deposit
• Oral-facial-digital syndrome with vaginal atresia, hydronephrosis and congenital cardiac defect
• Orofacial Clefts May Be a Window Into Identifying Common Psychopathology Development
• Orthodontic and Surgical Principles for Distraction Osteogenesis in Children with Pierre-Robin Sequence
• Orthodontic treatment of a patient with oral-facial-digital syndrome
• Papillon-Léage and psaume syndrome patient with multiple dental and orofacial anomalies
• Parental-Caregivers Perceptions Questionnaire (P-CPQ): translation and evaluation of psychometric properties of the French version of the questionnaire
• Pattern of cleft lip and palate in Dar-es-Salaam
• Peptide-modified Substrate for Modulating Gland Tissue Growth and Morphology In Vitro
• Prenatal diagnosis of a case probably with Oral-Facial-Digital Syndrome--Gabrielli type
• Prenatal sonographic findings in a case of Varadi-Papp syndrome
• Public health policy and medical missions in the Philippines: the case of oral--facial clefting
• Public health research at the CDC: implications for communication sciences and disorders
• Regulation of the epithelial adhesion molecule CEACAM1 is important for palate formation
• Runx1-Stat3-Tgfb3 signaling network regulating the anterior palatal development
• Sclt1 deficiency causes cystic kidney by activating ERK and STAT3 signaling
• Seasonal variation in birth months of patients with oral-facial clefts
• The inductive role of Wnt-β-Catenin signaling in the formation of oral apparatus
• The many faces of oral-facial-digital syndrome
• The Pittsburgh Oral-Facial Cleft study: expanding the cleft phenotype. Background and justification
• The Psychology of Patients With Oral-Facial Clefts: A Review of Victor Hugo's The Man Who Laughs (L'homme qui rit)
• Thurston syndrome: an uncommon disorder presenting with common abnormalities
• Transforming Growth Factor-Beta and Sonic Hedgehog Signaling in Palatal Epithelium Regulate Tenascin-C Expression in Palatal Mesenchyme During Soft Palate Development
• Translation and validation of the French version of the Child Perceptions Questionnaire for children aged from 8 to 10 years old (CPQ _8-10)
• Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome
• Using the avian mutant talpid2 as a disease model for understanding the oral-facial phenotypes of oral-facial-digital syndrome
• Varadi Papp syndrome, an unusual variant of oral-facial-digital syndrome: Report of a rare case
• Variability of expression of oral-facial-digital syndrome type I in 15 Saudi girls: Why is there a high rate of median cleft lip in the phenotype?
• Whole-Exon Sequencing and Correlation Analysis of a 14-Month-Old Girl With Orofaciodigital Syndrome
• X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia