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T N Mitchell

Showing results (1-10 of 14) with videos related to

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Transactions of the American Ophthalmological Society|January 1, 1990
Colobomatous malformations of the eyeI H Maumenee, T N Mitchell
Leprosy Review|August 2, 2000
The age-dependent deterioration in light touch sensation on the plantar aspect of the foot in a rural community in India: implications when screening for sensory impairmentP D Mitchell, T N Mitchell
Journal of the Royal College of Surgeons of Edinburgh|October 1, 1993
Three-dimensional endoscopic imaging for minimal access surgeryT N Mitchell, J Robertson, A G Nagy, et al.
American Journal of Medical Genetics|September 1, 1990
Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataractsF S Bodker, M A Lavery, T N Mitchell, et al.
Transactions of the American Ophthalmological Society|January 1, 1986
Inheritance of congenital esotropiaI H Maumenee, A Alston, M B Mets, et al.
Neurology|February 12, 2004
Defective auditory interhemispheric transfer in a patient with a PAX6 mutationD-E Bamiou, F E Musiek, S M Sisodiya, et al.
Neurology|April 24, 2002
Anterior commissure absence without callosal agenesis: a new brain malformationT N Mitchell, J M Stevens, S L Free, et al.
Human Molecular Genetics|May 1, 1997
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2M Litt, R Carrero-Valenzuela, D M LaMorticella, et al.
Nature Genetics|July 11, 2000
Genetic basis of total colourblindness among the Pingelapese islandersO H Sundin, J M Yang, Y Li, et al.
Human Genetics|November 1, 1990
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosomeD Zhu, D M Alcorn, S E Antonarakis, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Transactions of the American Ophthalmological Society|January 1, 1990
Colobomatous malformations of the eyeI H Maumenee, T N Mitchell
Leprosy Review|August 2, 2000
The age-dependent deterioration in light touch sensation on the plantar aspect of the foot in a rural community in India: implications when screening for sensory impairmentP D Mitchell, T N Mitchell
Journal of the Royal College of Surgeons of Edinburgh|October 1, 1993
Three-dimensional endoscopic imaging for minimal access surgeryT N Mitchell, J Robertson, A G Nagy, et al.
American Journal of Medical Genetics|September 1, 1990
Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataractsF S Bodker, M A Lavery, T N Mitchell, et al.
Transactions of the American Ophthalmological Society|January 1, 1986
Inheritance of congenital esotropiaI H Maumenee, A Alston, M B Mets, et al.
Neurology|February 12, 2004
Defective auditory interhemispheric transfer in a patient with a PAX6 mutationD-E Bamiou, F E Musiek, S M Sisodiya, et al.
Neurology|April 24, 2002
Anterior commissure absence without callosal agenesis: a new brain malformationT N Mitchell, J M Stevens, S L Free, et al.
Human Molecular Genetics|May 1, 1997
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2M Litt, R Carrero-Valenzuela, D M LaMorticella, et al.
Nature Genetics|July 11, 2000
Genetic basis of total colourblindness among the Pingelapese islandersO H Sundin, J M Yang, Y Li, et al.
Human Genetics|November 1, 1990
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosomeD Zhu, D M Alcorn, S E Antonarakis, et al.
Pageof 2