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Frances Flinter

Showing results (11-20 of 63) with videos related to

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European Journal of Human Genetics : EJHG|November 13, 2014
Clinical utility gene card for: Alport syndrome - update 2014Jens Michael Hertz, Mads Thomassen, Helen Storey, et al.
Journal of the American Society of Nephrology : JASN|January 26, 2013
Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathyJudy Savige, Martin Gregory, Oliver Gross, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2019
Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesisCaroline Pearce, Emma Goettke, Nina Hallowell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2019
Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesisCaroline Pearce, Emma Goettke, Nina Hallowell, et al.
Molecular Cytogenetics|February 26, 2009
A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case reportCaroline Mackie Ogilvie, Joo Wook Ahn, Kathy Mann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 25, 2010
Aortic abnormalities in males with Alport syndromeClifford E Kashtan, Yoav Segal, Frances Flinter, et al.
Nature Biotechnology|February 7, 2018
Corrigendum: Assisted reproductive technologies to prevent human mitochondrial disease transmissionAndy Greenfield, Peter Braude, Frances Flinter, et al.
Nature Biotechnology|July 7, 2018
Corrigendum: Assisted reproductive technologies to prevent human mitochondrial disease transmissionAndy Greenfield, Peter Braude, Frances Flinter, et al.
BJU International|August 12, 2014
The genetic diversity of cystinuria in a UK population of patientsKathie A Wong, Rachael Mein, Mark Wass, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 20, 2005
The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testingCaroline Mackie Ogilvie, Alison Lashwood, Lyn Chitty, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|November 13, 2014
Clinical utility gene card for: Alport syndrome - update 2014Jens Michael Hertz, Mads Thomassen, Helen Storey, et al.
Journal of the American Society of Nephrology : JASN|January 26, 2013
Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathyJudy Savige, Martin Gregory, Oliver Gross, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2019
Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesisCaroline Pearce, Emma Goettke, Nina Hallowell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2019
Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesisCaroline Pearce, Emma Goettke, Nina Hallowell, et al.
Molecular Cytogenetics|February 26, 2009
A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case reportCaroline Mackie Ogilvie, Joo Wook Ahn, Kathy Mann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 25, 2010
Aortic abnormalities in males with Alport syndromeClifford E Kashtan, Yoav Segal, Frances Flinter, et al.
Nature Biotechnology|February 7, 2018
Corrigendum: Assisted reproductive technologies to prevent human mitochondrial disease transmissionAndy Greenfield, Peter Braude, Frances Flinter, et al.
Nature Biotechnology|July 7, 2018
Corrigendum: Assisted reproductive technologies to prevent human mitochondrial disease transmissionAndy Greenfield, Peter Braude, Frances Flinter, et al.
BJU International|August 12, 2014
The genetic diversity of cystinuria in a UK population of patientsKathie A Wong, Rachael Mein, Mark Wass, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 20, 2005
The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testingCaroline Mackie Ogilvie, Alison Lashwood, Lyn Chitty, et al.
Pageof 7