نتایج جستجو برای: dysmorphology

تعداد نتایج: 421  

Journal: :Mechanisms of Development 2009
Randall J. Roper Justin F. VanHorn Colyn C. Cain Roger H. Reeves

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...

Journal: :Developmental dynamics : an official publication of the American Association of Anatomists 2010
Kristina Aldridge Cheryl A Hill Jordan R Austin Christopher Percival Neus Martinez-Abadias Thomas Neuberger Yingli Wang Ethylin Wang Jabs Joan T Richtsmeier

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...

Journal: :Developmental dynamics : an official publication of the American Association of Anatomists 2008
Mary Anne Potok Kelly B Cha Andrea Hunt Michelle L Brinkmeier Michael Leitges Andreas Kispert Sally A Camper

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...

Journal: :Journal of the International Neuropsychological Society : JINS 2008
Maureen Dennis Derryn Jewell Ross Hetherington Christine Burton Michael E Brandt Susan E Blaser Jack M Fletcher

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...

Journal: :Pathology 2023

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...

Journal: :Elektrotechnik und Informationstechnik 2008
Andreas Holzinger W. Emberger Siegfried Wassertheurer L. Neal

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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