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Journal of Medical Genetics
|
February 12, 2002
A locus for isolated cataract on human Xp
P J Francis, V Berry, A J Hardcastle, et al.
The Journal of Pathology
|
December 1, 1994
Characterization of a subtype of primary osteoclastoma: extracellular calcium but not calcitonin inhibits aggressive HLA-DR-positive osteoclastoma possessing 'functional' calcitonin receptors
H Rathod, A J Malcolm, J I Gillespie, et al.
The British Journal of Ophthalmology
|
January 25, 2005
Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene
P K F Addison, V Berry, A C W Ionides, et al.
Journal of the Mechanical Behavior of Biomedical Materials
|
September 22, 2020
Misinterpretation of ISO 4049 standard recommendations: Impact on Young's modulus and conversion degree of dental composites
C Özcan, P Lestriez, V Berry-Kromer, et al.
Human Molecular Genetics
|
September 26, 2000
Functional impairment of lens aquaporin in two families with dominantly inherited cataracts
P Francis, J J Chung, M Yasui, et al.
Molecular Vision
|
August 4, 2006
A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family
P K F Addison, V Berry, K R Holden, et al.
Antiviral Research
|
February 12, 2019
Proteolytic cleavage of host proteins by the Group IV viral proteases of Venezuelan equine encephalitis virus and Zika virus
Elaine M Morazzani, Jaimee R Compton, Dagmar H Leary, et al.
The British Journal of Ophthalmology
|
January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma
M A Reddy, P J Francis, V Berry, et al.
Journal of Affective Disorders
|
April 11, 2021
The longitudinal relationship between child emotional disorder and parental mental health in the British Child and Adolescent Mental Health surveys 1999 and 2004
K Wilkinson, S Ball, S B Mitchell, et al.
American Journal of Human Genetics
|
September 29, 2001
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
V Berry, P Francis, M A Reddy, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 77) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
February 12, 2002
A locus for isolated cataract on human Xp
P J Francis, V Berry, A J Hardcastle, et al.
The Journal of Pathology
|
December 1, 1994
Characterization of a subtype of primary osteoclastoma: extracellular calcium but not calcitonin inhibits aggressive HLA-DR-positive osteoclastoma possessing 'functional' calcitonin receptors
H Rathod, A J Malcolm, J I Gillespie, et al.
The British Journal of Ophthalmology
|
January 25, 2005
Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene
P K F Addison, V Berry, A C W Ionides, et al.
Journal of the Mechanical Behavior of Biomedical Materials
|
September 22, 2020
Misinterpretation of ISO 4049 standard recommendations: Impact on Young's modulus and conversion degree of dental composites
C Özcan, P Lestriez, V Berry-Kromer, et al.
Human Molecular Genetics
|
September 26, 2000
Functional impairment of lens aquaporin in two families with dominantly inherited cataracts
P Francis, J J Chung, M Yasui, et al.
Molecular Vision
|
August 4, 2006
A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family
P K F Addison, V Berry, K R Holden, et al.
Antiviral Research
|
February 12, 2019
Proteolytic cleavage of host proteins by the Group IV viral proteases of Venezuelan equine encephalitis virus and Zika virus
Elaine M Morazzani, Jaimee R Compton, Dagmar H Leary, et al.
The British Journal of Ophthalmology
|
January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma
M A Reddy, P J Francis, V Berry, et al.
Journal of Affective Disorders
|
April 11, 2021
The longitudinal relationship between child emotional disorder and parental mental health in the British Child and Adolescent Mental Health surveys 1999 and 2004
K Wilkinson, S Ball, S B Mitchell, et al.
American Journal of Human Genetics
|
September 29, 2001
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
V Berry, P Francis, M A Reddy, et al.
Page
of 8