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Clinical Genetics|April 18, 2021
Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two familiesFiona McKenzie, Kym Mina, Bert Callewaert, et al.
BMJ (Clinical Research Ed.)|March 11, 2010
Vitamin A supplementation and BCG vaccination at birth in low birthweight neonates: two by two factorial randomised controlled trialChristine Stabell Benn, Ane Baerent Fisker, Bitiguida Mutna Napirna, et al.
European Journal of Human Genetics : EJHG|May 13, 2024
Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohortSophia Hammer-Hansen, Ulrik Stoltze, Emil Bartels, et al.
The Journal of Infectious Diseases|June 16, 2011
Randomized trial of BCG vaccination at birth to low-birth-weight children: beneficial nonspecific effects in the neonatal period?Peter Aaby, Adam Roth, Henrik Ravn, et al.
European Journal of Medical Genetics|April 14, 2019
Phenotypic presentations of Hajdu-Cheney syndrome according to age - 5 distinct clinical presentationsLise Graversen, Mette Møller Handrup, Melita Irving, et al.
International Journal of Molecular Sciences|July 20, 2021
Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue FindingsIlse Van Gucht, Alice Krebsova, Birgitte Rode Diness, et al.
Journal of Medical Genetics|March 26, 2024
Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosisUmut Altunoglu, Adrian Palencia-Campos, Nilay Güneş, et al.
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