Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Frances Flinter

Showing results (1-10 of 63) with videos related to

Pageof 7
Sort By:
Reproductive Biomedicine Online|June 11, 2014
Concerning Tetsuya Ishii's article: potential impact of human mitochondrial replacement on global policy regarding germline gene modificationFrances Flinter
BMJ (Clinical Research Ed.)|May 23, 2013
Should we sequence everyone's genome? NoFrances Flinter
BMJ (Clinical Research Ed.)|September 8, 2007
Use and misuse of preimplantation genetic testingPeter Braude, Frances Flinter
Archives of Disease in Childhood|April 15, 2014
Familial haematuria: when to consider genetic testingJudy Taylor, Frances Flinter
Lancet (London, England)|October 4, 2005
Prenatal diagnosisCaroline Mackie Ogilvie, Frances Flinter
American Journal of Medical Genetics. Part A|November 24, 2017
Novel STRA6 null mutations in the original family described with Matthew-Wood syndromeFrancesca Pasutto, Frances Flinter, Anita Rauch, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 2, 2010
The value of clinical criteria in identifying patients with X-linked Alport syndromeHelen Hanson, Helen Storey, Judith Pagan, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
Clinical utility gene card for: Alport syndromeJens Michael Hertz, Mads Thomassen, Helen Storey, et al.
Nature Reviews. Genetics|December 3, 2002
Preimplantation genetic diagnosisPeter Braude, Susan Pickering, Frances Flinter, et al.
American Journal of Medical Genetics. Part A|April 10, 2014
Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndromeMichiala Cafferkey, Joo Wook Ahn, Frances Flinter, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Reproductive Biomedicine Online|June 11, 2014
Concerning Tetsuya Ishii's article: potential impact of human mitochondrial replacement on global policy regarding germline gene modificationFrances Flinter
BMJ (Clinical Research Ed.)|May 23, 2013
Should we sequence everyone's genome? NoFrances Flinter
BMJ (Clinical Research Ed.)|September 8, 2007
Use and misuse of preimplantation genetic testingPeter Braude, Frances Flinter
Archives of Disease in Childhood|April 15, 2014
Familial haematuria: when to consider genetic testingJudy Taylor, Frances Flinter
Lancet (London, England)|October 4, 2005
Prenatal diagnosisCaroline Mackie Ogilvie, Frances Flinter
American Journal of Medical Genetics. Part A|November 24, 2017
Novel STRA6 null mutations in the original family described with Matthew-Wood syndromeFrancesca Pasutto, Frances Flinter, Anita Rauch, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 2, 2010
The value of clinical criteria in identifying patients with X-linked Alport syndromeHelen Hanson, Helen Storey, Judith Pagan, et al.
European Journal of Human Genetics : EJHG|December 15, 2011
Clinical utility gene card for: Alport syndromeJens Michael Hertz, Mads Thomassen, Helen Storey, et al.
Nature Reviews. Genetics|December 3, 2002
Preimplantation genetic diagnosisPeter Braude, Susan Pickering, Frances Flinter, et al.
American Journal of Medical Genetics. Part A|April 10, 2014
Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndromeMichiala Cafferkey, Joo Wook Ahn, Frances Flinter, et al.
Pageof 7