खोज परिणाम - I. Christopher Lloyd

  • प्रदर्शित 1 - 10 परिणाम 10
परिणाम को परिष्कृत करें
  1. 1
    The ocular features of the mucopolysaccharidoses

    The ocular features of the mucopolysaccharidoses द्वारा Jane Ashworth, Susmito Biswas, Ed Wraith, I. Christopher Lloyd

    प्रकाशित 2005
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  2. 2
    Advances in the management of congenital and infantile cataract

    Advances in the management of congenital and infantile cataract द्वारा I. Christopher Lloyd, Jane Ashworth, Susmito Biswas, R V Abadi

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  3. 3
    A mutation in the RIEG1 gene associated with Peters’ anomaly

    A mutation in the RIEG1 gene associated with Peters’ anomaly द्वारा W Doward, Rahat Perveen, I. Christopher Lloyd, A E Ridgway, Laura C. Wilson, Graeme Black

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  4. 4
    Neonatal cataract: Aetiology, pathogenesis and management

    Neonatal cataract: Aetiology, pathogenesis and management द्वारा I. Christopher Lloyd, Mark Goss‐Sampson, Brett G. Jeffrey, A Kriss, I Russell‐Eggitt, David Taylor

    प्रकाशित 1992
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  5. 5
    Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis

    Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis द्वारा Graeme Black, Rahat Perveen, Richard Bonshek, Mark Cahill, Jill Clayton-Smith, I. Christopher Lloyd, David McLeod

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  6. 6
    Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach

    Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach द्वारा Mahmoud Musleh, Georgina Hall, I. Christopher Lloyd, Rachel Gillespie, S. Waller, Sofia Douzgou, Jill Clayton‐Smith, Elias Kehdi, Graeme Black, Jane Ashworth

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  7. 7
    Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric Cataract

    Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric Cataract द्वारा Rachel Gillespie, Jill Urquhart, Beverley Anderson, Simon G. Williams, Sarah Waller, Jane Ashworth, Susmito Biswas, Simon Jones, Fiona Stewart, I. Christopher Lloyd, Jill Clayton‐Smith, Graeme Black

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  8. 8
    Cataract management in children: a review of the literature and current practice across five large UK centres

    Cataract management in children: a review of the literature and current practice across five large UK centres द्वारा Jay Self, Rachel L. Taylor, Ameenat Lola Solebo, Susmito Biswas, Manoj Parulekar, Arundhati Dev Borman, Jane Ashworth, Rory McClenaghan, Joseph Abbott, Elizabeth O’Flynn, Darius Hildebrand, I. Christopher Lloyd

    प्रकाशित 2020
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  9. 9
    Molecular findings from 537 individuals with inherited retinal disease

    Molecular findings from 537 individuals with inherited retinal disease द्वारा Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, James O’Sullivan, Simon G. Williams, Janine A. Lamb, Binay Panda, Panagiotis I. Sergouniotis, Rachel Gillespie, Stephen P. Daiger, Georgina Hall, Theodora Gale, I. Christopher Lloyd, Paul N. Bishop, Simon Ramsden, Graeme Black

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  10. 10
    Mutations in<i>SIPA1L3</i>cause eye defects through disruption of cell polarity and cytoskeleton organization

    Mutations in<i>SIPA1L3</i>cause eye defects through disruption of cell polarity and cytoskeleton organization द्वारा Rebecca Greenlees, Marija Mihelec, Saira Yousoof, Daniel Speidel, Selwin K. Wu, Silke Rinkwitz, Ivan Prokudin, Rahat Perveen, Anson Cheng, Alan Ma, Benjamin M. Nash, Rachel Gillespie, David A.F. Loebel, Jill Clayton‐Smith, I. Christopher Lloyd, John Grigg, Patrick Tam, Alpha S. Yap, Thomas Becker, Graeme Black, Elena V. Semina, Robyn V. Jamieson

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:

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