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I C Lloyd

Showing results (41-50 of 48) with videos related to

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The British Journal of Ophthalmology|August 1, 1997
Anterior segment dysgenesis in mosaic Turner syndromeI C Lloyd, P M Haigh, J Clayton-Smith, et al.
Eye (London, England)|January 4, 2014
Anterior segment OCT imaging in mucopolysaccharidoses type I, II, and VIT Y Ahmed, A M J Turnbull, N F Attridge, et al.
European Journal of Medical Genetics|May 4, 2019
Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanismsA Redwood, S Douzgou, S Waller, et al.
Eye (London, England)|June 18, 2016
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approachM Musleh, G Hall, I C Lloyd, et al.
The Journal of Clinical Endocrinology and Metabolism|November 7, 2003
Endocrine status in patients with optic nerve hypoplasia: relationship to midline central nervous system abnormalities and appearance of the hypothalamic-pituitary axis on magnetic resonance imagingN H Birkebaek, L Patel, N B Wright, et al.
Eye (London, England)|August 12, 2020
Cataract management in children: a review of the literature and current practice across five large UK centresJ E Self, R Taylor, A L Solebo, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutationsR Perveen, I C Lloyd, J Clayton-Smith, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
The British Journal of Ophthalmology|August 1, 1997
Anterior segment dysgenesis in mosaic Turner syndromeI C Lloyd, P M Haigh, J Clayton-Smith, et al.
Eye (London, England)|January 4, 2014
Anterior segment OCT imaging in mucopolysaccharidoses type I, II, and VIT Y Ahmed, A M J Turnbull, N F Attridge, et al.
European Journal of Medical Genetics|May 4, 2019
Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanismsA Redwood, S Douzgou, S Waller, et al.
Eye (London, England)|June 18, 2016
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approachM Musleh, G Hall, I C Lloyd, et al.
The Journal of Clinical Endocrinology and Metabolism|November 7, 2003
Endocrine status in patients with optic nerve hypoplasia: relationship to midline central nervous system abnormalities and appearance of the hypothalamic-pituitary axis on magnetic resonance imagingN H Birkebaek, L Patel, N B Wright, et al.
Eye (London, England)|August 12, 2020
Cataract management in children: a review of the literature and current practice across five large UK centresJ E Self, R Taylor, A L Solebo, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutationsR Perveen, I C Lloyd, J Clayton-Smith, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Pageof 5