Showing results (31-40 of 36) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Acta Neurologica Scandinavica|November 18, 2003
The normal population distribution of PRNP codon 129 polymorphismM H Nurmi, M Bishop, L Strain, et al.Journal of Medical Genetics|July 10, 2007
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal gangliaY Saillour, G Zanni, V Des Portes, et al.American Journal of Human Genetics|July 1, 1994
Heterogeneity analysis in 40 X-linked retinitis pigmentosa familiesP W Teague, M A Aldred, M Jay, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 3, 2009
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850TA M Waters, I Pappworth, K Marchbank, et al.Communications Biology|March 29, 2024
Kir4.1 channels contribute to astrocyte CO2/H+-sensitivity and the drive to breatheColin M Cleary, Jack L Browning, Moritz Armbruster, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 17, 2012
Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantationJ H Brown, J Tellez, V Wilson, et al.Pageof 4