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

P Kannu

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Journal of Paediatrics and Child Health|December 1, 2004
Uncommon complication of herpes simplex encephalitisP Kannu, R Pinnock
Clinical Genetics|February 28, 2004
Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmedP Kannu, S Aftimos, I Winship
The British Journal of Dermatology|October 7, 2019
Aplasia cutis congenita associated with a heterozygous loss-of-function UBA2 variantY Wang, L Dupuis, R Jobling, et al.
Clinical Genetics|May 9, 2008
The skeletal manifestations of the congenital disorders of glycosylationD Coman, M Irving, P Kannu, et al.
Fetal Diagnosis and Therapy|July 29, 2010
Trisomy 16 mosaicism at chorionic villus sampling and amniocentesis with a normal physical and intellectual outcomeD Coman, R J M Gardner, M D Pertile, et al.
European Journal of Medical Genetics|June 25, 2013
Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5P Kannu, A B Campos-Xavier, D Hull, et al.
The British Journal of Dermatology|July 17, 2016
Mosaicism for a SPRED1 deletion revealed in a patient with clinically suspected mosaic neurofibromatosisR K Jobling, I Lara-Corrales, M-C Hsiao, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 31, 2019
Correction to: Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 28, 2019
Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
Clinical Genetics|April 27, 2012
Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutationP Kannu, M Nour, M Irving, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Paediatrics and Child Health|December 1, 2004
Uncommon complication of herpes simplex encephalitisP Kannu, R Pinnock
Clinical Genetics|February 28, 2004
Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmedP Kannu, S Aftimos, I Winship
The British Journal of Dermatology|October 7, 2019
Aplasia cutis congenita associated with a heterozygous loss-of-function UBA2 variantY Wang, L Dupuis, R Jobling, et al.
Clinical Genetics|May 9, 2008
The skeletal manifestations of the congenital disorders of glycosylationD Coman, M Irving, P Kannu, et al.
Fetal Diagnosis and Therapy|July 29, 2010
Trisomy 16 mosaicism at chorionic villus sampling and amniocentesis with a normal physical and intellectual outcomeD Coman, R J M Gardner, M D Pertile, et al.
European Journal of Medical Genetics|June 25, 2013
Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5P Kannu, A B Campos-Xavier, D Hull, et al.
The British Journal of Dermatology|July 17, 2016
Mosaicism for a SPRED1 deletion revealed in a patient with clinically suspected mosaic neurofibromatosisR K Jobling, I Lara-Corrales, M-C Hsiao, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 31, 2019
Correction to: Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 28, 2019
Hypophosphatasia: Canadian update on diagnosis and managementA A Khan, R Josse, P Kannu, et al.
Clinical Genetics|April 27, 2012
Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutationP Kannu, M Nour, M Irving, et al.
Pageof 2