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

Dan Doherty

Showing results (31-40 of 100) with videos related to

Pageof 10
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Interpreting the clinical significance of combined variants in multiple recessive disease genes: systematic investigation of Joubert syndrome yields little support for oligogenicityIan G Phelps, Jennifer C Dempsey, Megan E Grout, et al.
Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry|June 4, 2025
Behavioral Correlates of Caregiver-Reported Oral Health of Individuals With Joubert Syndrome: A Cross-Sectional Observational StudySai Win Kyaw Htet Aung, Joshua Orack, Dan Doherty, et al.
Nature Cell Biology|August 29, 2017
Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndromeXiaoyu Shi, Galo Garcia, Julie C Van De Weghe, et al.
Nature Cell Biology|November 1, 2017
Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndromeXiaoyu Shi, Galo Garcia, Julie C Van De Weghe, et al.
Stem Cell Reports|November 25, 2021
Rescuing human fetal tissue research in the United States: A call for additional regulatory reformKatherine E MacDuffie, Insoo Hyun, Michaela M Krogen, et al.
Journal of Child Neurology|July 18, 2015
Two Hundred Thirty-Six Children With Developmental Hydrocephalus: Causes and Clinical ConsequencesHannah M Tully, Gisele E Ishak, Tessa C Rue, et al.
Prenatal Diagnosis|June 21, 2005
Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRIDan Doherty, Ian A Glass, Joseph R Siebert, et al.
Pediatric Research|October 22, 2024
Early Intervention services in the era of genomic medicine: setting a research agendaKatherine E MacDuffie, Betty Cohn, Paul Appelbaum, et al.
American Journal of Human Genetics|December 17, 2008
Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosaAbdul Noor, Christian Windpassinger, Megha Patel, et al.
Brain : a Journal of Neurology|December 22, 2020
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeNancy Vegas, Karen Low, Christopher C Y Mak, et al.
Pageof 10

Showing results (31-40 of 100) with videos related to

Sort By:
Pageof 10
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Interpreting the clinical significance of combined variants in multiple recessive disease genes: systematic investigation of Joubert syndrome yields little support for oligogenicityIan G Phelps, Jennifer C Dempsey, Megan E Grout, et al.
Special Care in Dentistry : Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry|June 4, 2025
Behavioral Correlates of Caregiver-Reported Oral Health of Individuals With Joubert Syndrome: A Cross-Sectional Observational StudySai Win Kyaw Htet Aung, Joshua Orack, Dan Doherty, et al.
Nature Cell Biology|August 29, 2017
Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndromeXiaoyu Shi, Galo Garcia, Julie C Van De Weghe, et al.
Nature Cell Biology|November 1, 2017
Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndromeXiaoyu Shi, Galo Garcia, Julie C Van De Weghe, et al.
Stem Cell Reports|November 25, 2021
Rescuing human fetal tissue research in the United States: A call for additional regulatory reformKatherine E MacDuffie, Insoo Hyun, Michaela M Krogen, et al.
Journal of Child Neurology|July 18, 2015
Two Hundred Thirty-Six Children With Developmental Hydrocephalus: Causes and Clinical ConsequencesHannah M Tully, Gisele E Ishak, Tessa C Rue, et al.
Prenatal Diagnosis|June 21, 2005
Prenatal diagnosis in pregnancies at risk for Joubert syndrome by ultrasound and MRIDan Doherty, Ian A Glass, Joseph R Siebert, et al.
Pediatric Research|October 22, 2024
Early Intervention services in the era of genomic medicine: setting a research agendaKatherine E MacDuffie, Betty Cohn, Paul Appelbaum, et al.
American Journal of Human Genetics|December 17, 2008
Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosaAbdul Noor, Christian Windpassinger, Megha Patel, et al.
Brain : a Journal of Neurology|December 22, 2020
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeNancy Vegas, Karen Low, Christopher C Y Mak, et al.
Pageof 10