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THE INFLUENCE OF FGFR1 VARIANTS ON NORMAL HUMAN CRANIOFACIAL SHAPE [PDF]
, 2015 The factors influencing the morphology of the human face are of interest to researchers in a variety of different fields. Craniofacial morphology is modified by both genetic and epigenetic events, and factors influencing craniofacial morphology include ...
Kalra, Varun +4 more
core
Pathogenic de novo mutations increase with fathers' age and could be amplified through competition between genetically distinct subpopulations of spermatogonial stem cells (SSCs).
core
Apert Syndrome - caveats of squint management. [PDF]
Rom J Ophthalmol, 2023 Khurana R, Singh A, Kochhar D, Sundar S.
europepmc +1 more source
Anesthesia and Airway Management in Two Cases of Apert Syndrome: Case Reports
Eurasian Journal of Medicine, 2019 Apert syndrome is a type of acrocephalosyndactilia that consists of craniofacial synostosis, midface hypoplasia and syndactyly, with an autosomal dominant inheritance pattern.
Canan Atalay +3 more
doaj
Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers. [PDF]
Cureus, 2023 Kumari K +10 more
europepmc +1 more source
Brain and ventricular volume in patients with syndromic and complex craniosynostosis [PDF]
, 2011 T. de Jong +4 more
core +1 more source
Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice [PDF]
, 2010 Yingli Wang +10 more
core +1 more source
Outcome of Bilateral Hand Reconstruction in a Child Presenting Late With Apert Syndrome: A Case Report and Literature Review. [PDF]
Cureus, 2023 Lim B, Shalan M.
europepmc +1 more source