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Mostrando ítems 11-20 de 132
Caractéristiques cranio-faciales chez un groupe de patients chiliens atteints de fente labio-maxillo-palatine unilatérale opérée
(Elsevier Masson SAS, 2006)
Introduction. Craniofacial growth in cleft lip and palate patientsis controversial. Structural alterations of the face in these patientscould be due to the surgical treatment combined with the primaryvariations of the ...
Haplotype-based gene–gene interaction of bone morphogenetic protein 4 and interferon regulatory factor 6 in the etiology of non-syndromic cleft lip with or without cleft palate in a Chilean population
(Blackwell Munksgaard, 2017)
© 2017 Eur J Oral Sci Non-syndromic cleft lip with or without cleft palate (NSCL/P) is the most common craniofacial birth defect in humans, the etiology of which can be dependent on the interactions of multiple genes. We ...
Analysis of familial incidence of non-syndromic cleft lip and palate in a Brazilian population
(Medicina Oral S LValenciaEspanha, 2010)
Assessment of the association between SMAD1 and HHIP gene variation and non-syndromic cleft-lip palate in Chilean case-parent trios
(Brazilian Journal of Genetics, 2008)
Nonsyndromic cleft lip/palate (NSCLP) is a congenital malformation with features of a complex genetic trait. Several studies have reported positive association and linkage between NSCLP and microsatellite markers in the ...
Asociación entre polimorfismos del gen NAT2 y fisura labioleporina no sindrómica en ArgentinaAssociation between NAT2 polymorphisms with non-syndromic cleft lip with or without cleft palate in Argentina
(Soc Medica Santiago, 2015-04)
Background: NAT genes are considered candidate genes for the genetic predisposition to non-syndromic Cleft lip with or without cleft palate (NSCLP), since they codify for N-acetyltransferases, enzymes responsible for the ...
Linkage disequilibrium between msx1 and non-syndromic cleft lip/palate in the chilean population
(JOURNAL OF DENTAL RESEARCH, 2004)
The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review
(J Pediatr Genet, 2020-09-01)
The 22q11.2 deletion syndrome (22q11.2DS) is present in approximately 5 to 8% of patients with cleft lip, palate, or both (CL/P) and 75 to 80% of patients with congenital heart disease (CHD). In a literature review, we ...