Results 271 to 280 of about 252,362 (381)
Chromatinopathies (CP) are a growing group of rare genetic disorders characterized by cognitive deficits and growth abnormalities. This is the largest collection of CP to date, contributing to a deeper understanding of the landscape and diagnosis of these rare diseases, strongly improved by the use of large‐scale sequencing technologies.
Giulia Bruna Marchetti +16 more
wiley +1 more source
VividHairEdit is an advanced StyleGAN2 inversion system for high‐fidelity hair transfer and editing. Our system features improved structural integration, vibrant appearance representation, and optimized latent code selection, achieving superior generation quality and usability. A user‐friendly sketch interface enables precise modifications that reflect
Eunyeong Choi, Sihun Jin, Dongjoon Kim
wiley +1 more source
Surgical Outcomes and Complications of Distal Nasal Reconstruction: A Systematic Review and Meta-Analysis. [PDF]
Salzano G +7 more
europepmc +1 more source
Designing rehabilitation robots for the brain injured [PDF]
George, J., Gnanayutham, Paul
core
Family Media Practices in a Post‐Pandemic Future: Conversations From a Transglobal Research Project
ABSTRACT This article is co‐written by a team of researchers who worked together during the pandemic to conduct parallel research projects in their home countries, collectively referencing the project as Children, Media and Pandemic Parenting. Our article consists of a series of curated thought pieces, drawing on interviews with parents in Australia ...
Natalie Coulter +7 more
wiley +1 more source
Motorized semi-automated prism bar technique for enhanced prismatic evaluation. [PDF]
Suresh G +4 more
europepmc +1 more source
ABSTRACT For decades, children have been taught about ‘stranger danger’. Fear of the stranger has been associated with overly cautious parenting strategies, and the curtailing of freedoms as children transition to adolescents. This article aims to examine the extent to which parents consider this issue of stranger danger in their decisions to grant ...
Craig Collie
wiley +1 more source
Silver-Russell syndrome secondary to rare (epi)genotypes exhibits phenotypic heterogeneity challenging clinical diagnosis. [PDF]
Kurup U +5 more
europepmc +1 more source

