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W G Pearce

Showing results (41-50 of 52) with videos related to

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American Journal of Human Genetics|December 1, 1996
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25A J Mears, F Mirzayans, D B Gould, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1983
Autosomal dominant iridogoniodysgenesis: glaucoma managementH T Wyatt, W G Pearce, T A Boyd, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1983
Autosomal dominant iridogoniodysgenesis: genetic featuresW G Pearce, H T Wyatt, T A Boyd, et al.
The British Journal of Ophthalmology|March 1, 1992
Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafnessM P Clarke, T J Sullivan, C Francis, et al.
Birth Defects Original Article Series|January 1, 1982
Autosomal dominant iridogoniodysgenesis. A genetic and clinical studyW G Pearce, H T Wyatt, T A Boyd, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|April 1, 1995
Autosomal dominant keratitis: a possible aniridia variantW G Pearce, B W Mielke, D T Hassard, et al.
Human Genetics|October 6, 1998
Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23N T Bech-Hansen, K M Boycott, K J Gratton, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1987
Autosomal recessive juvenile cataract in HutteritesW G Pearce, J A Mackay, T M Holmes, et al.
Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.
Nature Genetics|July 14, 1998
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|December 1, 1996
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25A J Mears, F Mirzayans, D B Gould, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1983
Autosomal dominant iridogoniodysgenesis: glaucoma managementH T Wyatt, W G Pearce, T A Boyd, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 1, 1983
Autosomal dominant iridogoniodysgenesis: genetic featuresW G Pearce, H T Wyatt, T A Boyd, et al.
The British Journal of Ophthalmology|March 1, 1992
Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafnessM P Clarke, T J Sullivan, C Francis, et al.
Birth Defects Original Article Series|January 1, 1982
Autosomal dominant iridogoniodysgenesis. A genetic and clinical studyW G Pearce, H T Wyatt, T A Boyd, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|April 1, 1995
Autosomal dominant keratitis: a possible aniridia variantW G Pearce, B W Mielke, D T Hassard, et al.
Human Genetics|October 6, 1998
Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23N T Bech-Hansen, K M Boycott, K J Gratton, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1987
Autosomal recessive juvenile cataract in HutteritesW G Pearce, J A Mackay, T M Holmes, et al.
Human Genetics|April 1, 1990
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeN T Bech-Hansen, L L Field, A M Schramm, et al.
Nature Genetics|July 14, 1998
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Pageof 6