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B Jay

Showing results (31-40 of 68) with videos related to

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Journal of Medical Genetics|January 1, 1994
Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposisS V Hodgson, D T Bishop, B Jay
Eye (London, England)|January 1, 1988
Colour discrimination in pseudophakiaR A Harper, C M Kirkness, B Jay
Survey of Ophthalmology|September 1, 1985
AlbinismP E Kinnear, B Jay, C J Witkop
Birth Defects Original Article Series|January 1, 1976
Biochemical aspects of human albinismA F Winder, B Jay, R D Kissun
Birth Defects Original Article Series|January 1, 1982
Albinism in EnglandB Jay, C J Witkop, R A King
Eye (London, England)|January 1, 1987
Molecular genetic approaches to the analysis of human ophthalmic diseaseD N Cooper, M Jay, S Bhattacharya, et al.
JAMA Internal Medicine|March 7, 2022
Maybe Not an Acute Inferior Myocardial Infarction-ReplyDesmond B Jay, Timothy D Henry, Scott W Sharkey
JAMA Internal Medicine|December 6, 2021
Acute Inferior Myocardial Infarction or Not?Desmond B Jay, Timothy D Henry, Scott W Sharkey
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1994
Initiation codon mutation of the tyrosinase gene as a cause of human albinismL H Breimer, A F Winder, B Jay, et al.
Birth Defects Original Article Series|January 1, 1976
Human albinismB Jay, J Carruthers, M C Treplin, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|January 1, 1994
Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposisS V Hodgson, D T Bishop, B Jay
Eye (London, England)|January 1, 1988
Colour discrimination in pseudophakiaR A Harper, C M Kirkness, B Jay
Survey of Ophthalmology|September 1, 1985
AlbinismP E Kinnear, B Jay, C J Witkop
Birth Defects Original Article Series|January 1, 1976
Biochemical aspects of human albinismA F Winder, B Jay, R D Kissun
Birth Defects Original Article Series|January 1, 1982
Albinism in EnglandB Jay, C J Witkop, R A King
Eye (London, England)|January 1, 1987
Molecular genetic approaches to the analysis of human ophthalmic diseaseD N Cooper, M Jay, S Bhattacharya, et al.
JAMA Internal Medicine|March 7, 2022
Maybe Not an Acute Inferior Myocardial Infarction-ReplyDesmond B Jay, Timothy D Henry, Scott W Sharkey
JAMA Internal Medicine|December 6, 2021
Acute Inferior Myocardial Infarction or Not?Desmond B Jay, Timothy D Henry, Scott W Sharkey
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1994
Initiation codon mutation of the tyrosinase gene as a cause of human albinismL H Breimer, A F Winder, B Jay, et al.
Birth Defects Original Article Series|January 1, 1976
Human albinismB Jay, J Carruthers, M C Treplin, et al.
Pageof 7