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Scandinavian Journal of Rheumatology|January 1, 1986
Increased collagenase activity in human rheumatoid meniscusS Lindy, H Turto, T Sorsa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2017
High frequency of mosaic pathogenic variants in genes causing epilepsy-related neurodevelopmental disordersMary Beth Stosser, Amanda S Lindy, Elizabeth Butler, et al.
American Journal of Medical Genetics. Part A|June 14, 2014
Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani-Lenz syndromeAmanda S Lindy, Caleb P Bupp, Stephen J McGee, et al.
American Journal of Medical Genetics. Part A|March 31, 2016
Identification of a novel insertion mutation in FGFR3 that causes thanatophoric dysplasia type 1Amanda S Lindy, Monica J Basehore, Mumingjiang Munisha, et al.
Development (Cambridge, England)|June 23, 2006
An antagonistic role for the C. elegans Schnurri homolog SMA-9 in modulating TGFbeta signaling during mesodermal patterningMarisa L Foehr, Amanda S Lindy, Rachel C Fairbank, et al.
Epilepsia|April 15, 2018
Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disordersAmanda S Lindy, Mary Beth Stosser, Elizabeth Butler, et al.
Brain : a Journal of Neurology|March 14, 2020
A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variantsJavier A López-Rivera, Eduardo Pérez-Palma, Joseph Symonds, et al.
Nature Communications|September 3, 2014
TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviourAmanda S Lindy, Puja K Parekh, Richard Zhu, et al.
JCI Insight|February 1, 2022
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneityCarlos G Vanoye, Reshma R Desai, Zhigang Ji, et al.
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