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Journal of Medical Genetics|July 29, 1999
Fragile X syndrome with FMR1 and FMR2 deletionS J Moore, L Strain, G F Cole, et al.
Prenatal Diagnosis|June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutationL Strain, M E Porteous, C M Gosden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 2001
Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian familyG G Kovács, C Ertsey, C Majtényi, et al.
Science (New York, N.Y.)|May 23, 1986
Propolypeptide of von Willebrand factor circulates in blood and is identical to von Willebrand antigen IIP J Fay, Y Kawai, D D Wagner, et al.
Frontiers in Psychology|August 25, 2023
The role of individual differences in resistance to persuasion on memory for political advertisementsStuart S Miller, John P Hutson, Megan L Strain, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 8, 2006
Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutationJ M Saland, S H Emre, B L Shneider, et al.
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