نتایج جستجو برای: dysmorphology
تعداد نتایج: 421 فیلتر نتایج به سال:
Trisomy 21 results in phenotypes collectively referred to as Down syndrome (DS) including characteristic facial dysmorphology. Ts65Dn mice are trisomic for orthologs of about half of the genes found on human chromosome 21 and exhibit DS-like craniofacial abnormalities, including a small dysmorphic mandible. Quantitative analysis of neural crest (NC) progenitors of the mandible revealed a paucit...
Apert syndrome (AS) is one of at least nine disorders considered members of the fibroblast growth factor receptor (FGFR) -1, -2, and -3-related craniosynostosis syndromes. Nearly 100% of individuals diagnosed with AS carry one of two neighboring mutations on Fgfr2. The cranial phenotype associated with these two mutations includes coronal suture synostosis, either unilateral (unicoronal synosto...
We examined the role of WNT signaling in pituitary development by characterizing the pituitary phenotype of three WNT knockout mice and assessing the expression of WNT pathway components. Wnt5a mutants have expanded domains of Fgf10 and bone morphogenetic protein expression in the ventral diencephalon and a reduced domain of LHX3 expression in Rathke's pouch. Wnt4 mutants have mildly reduced ce...
We investigated verb generation in children with spina bifida meningomyelocele (SBM; n = 55) and in typically developing controls (n = 32). Participants completed 6 blocks (40 trials each) of a task requiring them to produce a semantically related verb in response to a target noun and an additional 40 trials on which they were simply required to read target nouns aloud. After controlling for re...
Whilst modern imaging modalities have far advanced antenatal diagnoses, the perinatal autopsy remains gold standard in confirming and assessing fetal dysmorphology. The presence of multiple abnormalities involving several organ systems raises clinical suspicion an underlying genetic syndrome. Our case involves a nulliparous woman her third decade life with unmarkable medical familial history. S...
Objective: In this paper, the authors describe the design, development and evaluationof specific simulation software for Cytogenetics training in order to demonstrate the usefulness of computer simulations for both teaching and learning of complex educational content. Background: Simulations have a long tradition inmedicine and can be very helpful for learning complex content, for example Cytog...
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