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Estudio de asociación entre la fisura labiopalatina no sindrómica y marcadores de microsatélite ubicados en 6p
(Sociedad Médica de Santiago, 1999)
Incontinentia pigmenti associated to cleft palate. Case report and literature review
(Facultad de Odontología, 2012)
Relationship between interpregnancy interval and birth defects in Washington State
(Springer, 2012)
Objective: Interpregnancy interval (IPI) influences numerous adverse perinatal outcomes. IPI's impact on birth defects is unclear. Study Design:We conducted a population-based case-control study, using 1998 to 2008 ...
Dorsal Displacement of the Soft Palate Secondary to Persistent Frenulum of the Epiglottis in Neonatal Foal
(2020-04-01)
Dorsal displacement of the soft palate (DDSP) usually occurs in athletic adult horses. Congenital DDSP in foals secondary to the persistent frenulum of the epiglottis is rarely observed. The aim of this report was to ...
Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate
(2009-12-01)
Phenotypically discordant monozygotic twins offer the possibility of gene discovery through delineation of molecular abnormalities in one member of the twin pair. One proposed mechanism of discordance is postzygotically ...
Inflammatory Papillary Hyperplasia of the Palate: Quantitative Analysis of Candida albicans and its Negative Correlation with Microscopic and Demographic Aspects
(QUINTESSENCE PUBLISHING CO INC, 2011)
Inflammatory papillary hyperplasia of the palate (IPHP) is a tissue-reactive overgrowth characterized by hyperemic mucosa with nodular or papillary appearance in the palate. The exact pathogenesis is still unclear. In this ...
Blepharocheilodontic (BCD) syndrome: Expanding the phenotype?
(2003-09-01)
We describe affected individuals in three generations of a family and another sporadic case, all Brazilian patients, with a combination of signs that diagnose the BCD syndrome. In addition to the cardinal signs, the sporadic ...
Blepharocheilodontic (BCD) syndrome: Expanding the phenotype?
(2003-09-01)
We describe affected individuals in three generations of a family and another sporadic case, all Brazilian patients, with a combination of signs that diagnose the BCD syndrome. In addition to the cardinal signs, the sporadic ...