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

Lucy Jenkins

Showing results (11-20 of 39) with videos related to

Pageof 4
Sort By:
The New England Journal of Medicine|October 27, 2016
Child-Parent Familial Hypercholesterolemia Screening in Primary CareDavid S Wald, Jonathan P Bestwick, Joan K Morris, et al.
Prenatal Diagnosis|April 18, 2013
The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress madeNicholas Lench, Angela Barrett, Sarah Fielding, et al.
Development and Psychopathology|March 15, 2002
Preschool children with disruptive behavior: three-year outcome as a function of adaptive disabilityRussell A Barkley, Terri L Shelton, Cheryl Crosswait, et al.
Pediatric Nephrology (Berlin, Germany)|February 12, 2017
Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.
Prenatal Diagnosis|February 25, 2015
Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysisMelissa Hill, Philip Twiss, Talitha I Verhoef, et al.
Clinical Kidney Journal|June 27, 2018
Clinical and diagnostic features of Bartter and Gitelman syndromesPatrick R Walsh, Yincent Tse, Emma Ashton, et al.
Pediatric Nephrology (Berlin, Germany)|March 5, 2017
Erratum to: Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.
Genes|June 28, 2023
A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in <i>RS1</i>, and Skewed X-InactivationJennifer Kirkby, Stephanie Halford, Morag Shanks, et al.
Prenatal Diagnosis|February 16, 2019
Ensuring high standards for the delivery of NIPT world-wide: Development of an international external quality assessment schemeZandra C Deans, Stephanie Allen, Lucy Jenkins, et al.
Clinical Chemistry|September 26, 2019
Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and ImplicationsNatalie J Chandler, Helena Ahlfors, Suzanne Drury, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
The New England Journal of Medicine|October 27, 2016
Child-Parent Familial Hypercholesterolemia Screening in Primary CareDavid S Wald, Jonathan P Bestwick, Joan K Morris, et al.
Prenatal Diagnosis|April 18, 2013
The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress madeNicholas Lench, Angela Barrett, Sarah Fielding, et al.
Development and Psychopathology|March 15, 2002
Preschool children with disruptive behavior: three-year outcome as a function of adaptive disabilityRussell A Barkley, Terri L Shelton, Cheryl Crosswait, et al.
Pediatric Nephrology (Berlin, Germany)|February 12, 2017
Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.
Prenatal Diagnosis|February 25, 2015
Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysisMelissa Hill, Philip Twiss, Talitha I Verhoef, et al.
Clinical Kidney Journal|June 27, 2018
Clinical and diagnostic features of Bartter and Gitelman syndromesPatrick R Walsh, Yincent Tse, Emma Ashton, et al.
Pediatric Nephrology (Berlin, Germany)|March 5, 2017
Erratum to: Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.
Genes|June 28, 2023
A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in <i>RS1</i>, and Skewed X-InactivationJennifer Kirkby, Stephanie Halford, Morag Shanks, et al.
Prenatal Diagnosis|February 16, 2019
Ensuring high standards for the delivery of NIPT world-wide: Development of an international external quality assessment schemeZandra C Deans, Stephanie Allen, Lucy Jenkins, et al.
Clinical Chemistry|September 26, 2019
Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and ImplicationsNatalie J Chandler, Helena Ahlfors, Suzanne Drury, et al.
Pageof 4