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L Strain

Showing results (31-40 of 43) with videos related to

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Prenatal Diagnosis|October 1, 1988
First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypesA Curtis, L Strain, M Mennie, et al.
Journal of Medical Genetics|August 1, 1997
Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorderD R FitzPatrick, L Strain, A E Thomas, 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.
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.
Journal of Medical Genetics|October 4, 2002
A novel atypical 22q11.2 distal deletion in father and sonS Garcia-Miñaur, J Fantes, R S Murray, et al.
American Journal of Human Genetics|November 1, 1991
Risk calculation in retinitis pigmentosaS M Holloway, L Strain, A E Shrimpton, 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.
Journal of Medical Genetics|March 24, 2005
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsV Fremeaux-Bacchi, E J Kemp, J A Goodship, et al.
Acta Neurologica Scandinavica|November 18, 2003
The normal population distribution of PRNP codon 129 polymorphismM H Nurmi, M Bishop, L Strain, 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.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|October 1, 1988
First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypesA Curtis, L Strain, M Mennie, et al.
Journal of Medical Genetics|August 1, 1997
Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorderD R FitzPatrick, L Strain, A E Thomas, 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.
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.
Journal of Medical Genetics|October 4, 2002
A novel atypical 22q11.2 distal deletion in father and sonS Garcia-Miñaur, J Fantes, R S Murray, et al.
American Journal of Human Genetics|November 1, 1991
Risk calculation in retinitis pigmentosaS M Holloway, L Strain, A E Shrimpton, 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.
Journal of Medical Genetics|March 24, 2005
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsV Fremeaux-Bacchi, E J Kemp, J A Goodship, et al.
Acta Neurologica Scandinavica|November 18, 2003
The normal population distribution of PRNP codon 129 polymorphismM H Nurmi, M Bishop, L Strain, 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.
Pageof 5