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Early Human Development, ISSN 0378-3782, 08/2019, Volume 135, pp. 23 - 26
The cleft lip with or without palate is the most common congenital craniofacial anomaly, presenting prevalence that varies between different ethnicities. It... 
Etiology | Nonsyndromic oral cleft | Parental consanguinity | LIP | GENES | PEDIATRICS | PREVALENCE | PALATE | OBSTETRICS & GYNECOLOGY | Parenting | Risk factors | Genetic disorders
Journal Article
Archives of Oral Biology, ISSN 0003-9969, 01/2020, Volume 109, p. 104556
To investigate the association of rs12532 polymorphism with the risk of nonsyndromic unilateral complete cleft lip and palate (NSCLP) and tooth agenesis. The... 
Tooth agenesis | Single nucleotide polymorphism | MSX1 | Nonsyndromic cleft lip and palate | Risk factor
Journal Article
RSBO, ISSN 1806-7727, 04/2012, Volume 9, Issue 2, pp. 151 - 157
Introduction: Cleft lip and palate anomalies are malformations that affect patients causing some alterations. These alterations can compromise maternal nursing... 
Sucrose | Plastic surgery | Infants | Mothers | Feeding | Ingestion | Babies | Alterations | Nursing | Nurses | Rehabilitation | Children | Habits | Milk | Anomalies
Journal Article
Journal Article
Journal of Clinical Periodontology, ISSN 0303-6979, 04/2012, Volume 39, Issue 4, pp. 323 - 332
Journal Article
Journal of Applied Oral Science, ISSN 1678-7765, 12/2016, Volume 24, Issue 6, pp. 549 - 554
ABSTRACT The early recognition of risk factors for the occurrence of palatally displaced canines (PDC) can increase the possibility of impaction prevention.... 
DENTISTRY, ORAL SURGERY & MEDICINE
Journal Article
The Cleft Palate-Craniofacial Journal, ISSN 1055-6656, 7/2009, Volume 46, Issue 4, pp. 420 - 424
Journal Article
Cleft Palate-Craniofacial Journal, ISSN 1055-6656, 03/2003, Volume 40, Issue 2, pp. 172 - 175
Journal Article
Cleft lip and palate and tooth agenesis are considered changes in embryonic development. These phenotypes occur as a result of the interaction of genetic and... 
Anodontia | Cleft lip | Biologia molecular | Molecular Biology | Genetics | Cleft Palate | Fenda labial | Genética | Fissura palatina
Dissertation
Journal of Applied Oral Science, ISSN 1678-7757, 12/2006, Volume 14, Issue 6, pp. 465 - 469
INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this... 
Craniossinostose | Mouth abnormalities | Anomalias dentárias | Tooth eruption | Craniosynostoses | Acrocefalosindactilia | Tooth abnormalities | Irrupção dentária ectópica | Acrocephalosyndactylia | ectopic | Alterações bucais
Journal Article
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