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

D Hewett

Showing results (81-90 of 93) with videos related to

Pageof 10
Sort By:
Journal of Lipid Research|February 1, 1989
Development and partial metabolic characterization of a dietary cholesterol-resistant colony of rabbitsM L Overturf, S A Smith, D Hewett-Emmett, et al.
Vision Research|January 20, 1999
Molecular evolution of trichromacy in primatesD M Hunt, K S Dulai, J A Cowing, et al.
The New England Journal of Medicine|April 2, 1992
Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative StudyP Tsipouras, R Del Mastro, M Sarfarazi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1992
Educational, occupational, and insurance status of childhood cancer survivors in their fourth and fifth decades of lifeD M Hays, J Landsverk, S E Sallan, et al.
The New England Journal of Medicine|July 18, 1985
Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificationW S Sly, M P Whyte, V Sundaram, et al.
Cell|February 7, 1997
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatS Yu, M Mangelsdorf, D Hewett, et al.
American Journal of Human Genetics|October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2M Horwitz, K F Benson, F Q Li, et al.
Ethnicity & Disease|January 1, 1993
An ultrasound survey of gallbladder disease among Mexican Americans in Starr County, Texas: frequencies and risk factorsC L Hanis, D Hewett-Emmett, L F Kubrusly, et al.
Genetics|April 2, 1999
High polymorphism at the human melanocortin 1 receptor locusB K Rana, D Hewett-Emmett, L Jin, et al.
Human Biology|July 19, 2001
Skin reflectance in the Han Chinese and Tibetan populationsH Wu, H Wang, H Li, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Journal of Lipid Research|February 1, 1989
Development and partial metabolic characterization of a dietary cholesterol-resistant colony of rabbitsM L Overturf, S A Smith, D Hewett-Emmett, et al.
Vision Research|January 20, 1999
Molecular evolution of trichromacy in primatesD M Hunt, K S Dulai, J A Cowing, et al.
The New England Journal of Medicine|April 2, 1992
Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative StudyP Tsipouras, R Del Mastro, M Sarfarazi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 1992
Educational, occupational, and insurance status of childhood cancer survivors in their fourth and fifth decades of lifeD M Hays, J Landsverk, S E Sallan, et al.
The New England Journal of Medicine|July 18, 1985
Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificationW S Sly, M P Whyte, V Sundaram, et al.
Cell|February 7, 1997
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatS Yu, M Mangelsdorf, D Hewett, et al.
American Journal of Human Genetics|October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2M Horwitz, K F Benson, F Q Li, et al.
Ethnicity & Disease|January 1, 1993
An ultrasound survey of gallbladder disease among Mexican Americans in Starr County, Texas: frequencies and risk factorsC L Hanis, D Hewett-Emmett, L F Kubrusly, et al.
Genetics|April 2, 1999
High polymorphism at the human melanocortin 1 receptor locusB K Rana, D Hewett-Emmett, L Jin, et al.
Human Biology|July 19, 2001
Skin reflectance in the Han Chinese and Tibetan populationsH Wu, H Wang, H Li, et al.
Pageof 10