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E Craig

Showing results (731-740 of 1,029) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in TasmaniaA I McNaught, J G Allen, D L Healey, et al.
Ophthalmology|February 22, 2023
Mitochondrial TXNRD2 and ME3 Genetic Risk Scores Are Associated with Specific Primary Open-Angle Glaucoma PhenotypesInas F Aboobakar, Tyler G Kinzy, Yan Zhao, et al.
Journal of Pediatric Hematology/Oncology|May 1, 1995
A phase I and II trial of dose-intensified cyclophosphamide and GM-CSF in pediatric malignant brain tumorsT G Abrahamsen, B J Lange, R J Packer, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 25, 2005
Prevalence of diabetes complications 6 years after diagnosis in an incident cohort of childhood diabetesK C Donaghue, M E Craig, A K F Chan, et al.
American Journal of Human Genetics|June 2, 2021
Automated AI labeling of optic nerve head enables insights into cross-ancestry glaucoma risk and genetic discovery in >280,000 images from UKB and CLSAXikun Han, Kaiah Steven, Ayub Qassim, et al.
Journal of Paediatrics and Child Health|June 21, 2013
Response to growth hormone treatment in Prader-Willi syndrome: auxological criteria versus genetic diagnosisElly Scheermeyer, Ian Hughes, Mark Harris, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Central corneal thickness is highly heritable: the twin eye studiesTze'Yo Toh, S H Melissa Liew, Jane R MacKinnon, et al.
Archives of Disease in Childhood|June 10, 2011
Increased detection of cystic-fibrosis-related diabetes in AustraliaMalay Rana, Craig F Munns, Hiran C Selvadurai, et al.
European Journal of Human Genetics : EJHG|April 19, 2021
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataractJohanna L Jones, Mark A Corbett, Elise Yeaman, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Pageof 103

Showing results (731-740 of 1,029) with videos related to

Sort By:
Pageof 103
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in TasmaniaA I McNaught, J G Allen, D L Healey, et al.
Ophthalmology|February 22, 2023
Mitochondrial TXNRD2 and ME3 Genetic Risk Scores Are Associated with Specific Primary Open-Angle Glaucoma PhenotypesInas F Aboobakar, Tyler G Kinzy, Yan Zhao, et al.
Journal of Pediatric Hematology/Oncology|May 1, 1995
A phase I and II trial of dose-intensified cyclophosphamide and GM-CSF in pediatric malignant brain tumorsT G Abrahamsen, B J Lange, R J Packer, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 25, 2005
Prevalence of diabetes complications 6 years after diagnosis in an incident cohort of childhood diabetesK C Donaghue, M E Craig, A K F Chan, et al.
American Journal of Human Genetics|June 2, 2021
Automated AI labeling of optic nerve head enables insights into cross-ancestry glaucoma risk and genetic discovery in >280,000 images from UKB and CLSAXikun Han, Kaiah Steven, Ayub Qassim, et al.
Journal of Paediatrics and Child Health|June 21, 2013
Response to growth hormone treatment in Prader-Willi syndrome: auxological criteria versus genetic diagnosisElly Scheermeyer, Ian Hughes, Mark Harris, et al.
Investigative Ophthalmology & Visual Science|September 28, 2005
Central corneal thickness is highly heritable: the twin eye studiesTze'Yo Toh, S H Melissa Liew, Jane R MacKinnon, et al.
Archives of Disease in Childhood|June 10, 2011
Increased detection of cystic-fibrosis-related diabetes in AustraliaMalay Rana, Craig F Munns, Hiran C Selvadurai, et al.
European Journal of Human Genetics : EJHG|April 19, 2021
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataractJohanna L Jones, Mark A Corbett, Elise Yeaman, et al.
Human Mutation|September 27, 2002
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 geneMichèle M Sale, Jamie E Craig, Jacinta C Charlesworth, et al.
Pageof 103