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David Ravine

Showing results (21-30 of 31) with videos related to

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European Journal of Human Genetics : EJHG|August 4, 2005
p.R270X MECP2 mutation and mortality in Rett syndromeLe Jian, Hayley L Archer, David Ravine, et al.
Diabetes Care|April 7, 2010
Maternal family history of diabetes is associated with a reduced risk of cardiovascular disease in women with type 2 diabetes: the Fremantle Diabetes StudyDavid G Bruce, Kylie Van Minnen, Wendy A Davis, et al.
Journal of Medical Genetics|August 15, 2006
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivationHayley Archer, Julie Evans, Helen Leonard, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|June 2, 2009
Cells of epithelial lineage are present in blood, engraft the bronchial epithelium, and are increased in human lung transplantationLeigh A May, Anthony Kicic, Paul Rigby, et al.
Molecular Genetics & Genomic Medicine|December 10, 2017
A review of structural brain abnormalities in Pallister-Killian syndromeCathryn Poulton, Gareth Baynam, Clarissa Yates, et al.
Molecular Autism|December 8, 2017
Cytokine levels and associations with symptom severity in male and female children with autism spectrum disorderAnne Masi, Edmond J Breen, Gail A Alvares, et al.
Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.
Nature Genetics|March 30, 2007
Analysis of published PKD1 gene sequence variantsAlexander M Gout, , David Ravine, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|August 4, 2005
p.R270X MECP2 mutation and mortality in Rett syndromeLe Jian, Hayley L Archer, David Ravine, et al.
Diabetes Care|April 7, 2010
Maternal family history of diabetes is associated with a reduced risk of cardiovascular disease in women with type 2 diabetes: the Fremantle Diabetes StudyDavid G Bruce, Kylie Van Minnen, Wendy A Davis, et al.
Journal of Medical Genetics|August 15, 2006
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivationHayley Archer, Julie Evans, Helen Leonard, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|June 2, 2009
Cells of epithelial lineage are present in blood, engraft the bronchial epithelium, and are increased in human lung transplantationLeigh A May, Anthony Kicic, Paul Rigby, et al.
Molecular Genetics & Genomic Medicine|December 10, 2017
A review of structural brain abnormalities in Pallister-Killian syndromeCathryn Poulton, Gareth Baynam, Clarissa Yates, et al.
Molecular Autism|December 8, 2017
Cytokine levels and associations with symptom severity in male and female children with autism spectrum disorderAnne Masi, Edmond J Breen, Gail A Alvares, et al.
Journal of the American Society of Nephrology : JASN|October 24, 2008
Unified criteria for ultrasonographic diagnosis of ADPKDYork Pei, James Obaji, Annie Dupuis, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.
Nature Genetics|March 30, 2007
Analysis of published PKD1 gene sequence variantsAlexander M Gout, , David Ravine, et al.
Pageof 4