Resultados da busca - Andrew O.M. Wilkie

Refinar Resultados
  1. 1
    Craniosynostosis: genes and mechanisms

    Craniosynostosis: genes and mechanisms por Andrew O.M. Wilkie

    Publicado em 1997
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  2. 2
    The molecular basis of genetic dominance.

    The molecular basis of genetic dominance. por Andrew O.M. Wilkie

    Publicado em 1994
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  3. 3
    Paternal Age Effect Mutations and Selfish Spermatogonial Selection: Causes and Consequences for Human Disease

    Paternal Age Effect Mutations and Selfish Spermatogonial Selection: Causes and Consequences for Human Disease por Anne Goriely, Andrew O.M. Wilkie

    Publicado em 2012
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  4. 4
    Craniosynostosis

    Craniosynostosis por David Johnson, Andrew O.M. Wilkie

    Publicado em 2011
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  5. 5
    Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

    Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies por Gillian Morriss‐Kay, Andrew O.M. Wilkie

    Publicado em 2005
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  6. 6
    A Genetic-Pathophysiological Framework for Craniosynostosis

    A Genetic-Pathophysiological Framework for Craniosynostosis por Stephen R.F. Twigg, Andrew O.M. Wilkie

    Publicado em 2015
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  7. 7
    New insights into craniofacial malformations

    New insights into craniofacial malformations por Stephen R.F. Twigg, Andrew O.M. Wilkie

    Publicado em 2015
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  8. 8
    Cellular evidence for selfish spermatogonial selection in aged human testes

    Cellular evidence for selfish spermatogonial selection in aged human testes por Geoffrey J. Maher, Anne Goriely, Andrew O.M. Wilkie

    Publicado em 2013
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  9. 9
    Clinical genetics of craniosynostosis

    Clinical genetics of craniosynostosis por Andrew O.M. Wilkie, David Johnson, Steven A. Wall

    Publicado em 2017
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  10. 10
    Functions of fibroblast growth factors and their receptors

    Functions of fibroblast growth factors and their receptors por Andrew O.M. Wilkie, Gillian Morriss‐Kay, E. Yvonne Jones, John K. Heath

    Publicado em 1995
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  11. 11
    Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

    Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand por Jane Anderson, Helen D. Burns, Pita Enriquez-Harris, Andrew O.M. Wilkie, John K. Heath

    Publicado em 1998
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  12. 12
    “Selfish Spermatogonial Selection”: A Novel Mechanism for the Association Between Advanced Paternal Age and Neurodevelopmental Disorders

    “Selfish Spermatogonial Selection”: A Novel Mechanism for the Association Between Advanced Paternal Age and Neurodevelopmental Disorders por Anne Goriely, John J. McGrath, Christina M. Hultman, Andrew O.M. Wilkie, Dolores Malaspina

    Publicado em 2013
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  13. 13
    Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes

    Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes por Geoffrey J. Maher, Simon J. McGowan, Eleni Giannoulatou, Clare Verrill, Anne Goriely, Andrew O.M. Wilkie

    Publicado em 2016
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  14. 14
    A review of the molecular genetics of the human alpha-globin gene cluster

    A review of the molecular genetics of the human alpha-globin gene cluster por DR Higgs, Mark A. Vickers, Andrew O.M. Wilkie, IM Pretorius, Andrew P. Jarman, D. J. Weatherall

    Publicado em 1989
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  15. 15
    A review of the molecular genetics of the human alpha-globin gene cluster

    A review of the molecular genetics of the human alpha-globin gene cluster por DR Higgs, Mark A. Vickers, Andrew O.M. Wilkie, IM Pretorius, Andrew P. Jarman, D. J. Weatherall

    Publicado em 1989
    Obter o texto integral Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  16. 16
    The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

    The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation por Jonathan Flint, Andrew O.M. Wilkie, Veronica J. Buckle, Robin M. Winter, Anthony Holland, Heather E. McDermid

    Publicado em 1995
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  17. 17
    Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype

    Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype por Lampros A. Mavrogiannis, Indira B. Taylor, Sally Davies, Feliciano J. Ramos, José L. Olivares, Andrew O.M. Wilkie

    Publicado em 2005
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  18. 18
    Hearing loss in a mouse model of Muenke syndrome

    Hearing loss in a mouse model of Muenke syndrome por Suzanne L. Mansour, Stephen R.F. Twigg, Rowena M. Freeland, Steven A. Wall, Zesong Li, Andrew O.M. Wilkie

    Publicado em 2008
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  19. 19
    A variant in the sonic hedgehog regulatory sequence (ZRS) is associated with triphalangeal thumb and deregulates expression in the developing limb

    A variant in the sonic hedgehog regulatory sequence (ZRS) is associated with triphalangeal thumb and deregulates expression in the developing limb por Dominic Furniss, Laura A. Lettice, Indira B. Taylor, Paul Critchley, Henk Giele, Robert E. Hill, Andrew O.M. Wilkie

    Publicado em 2008
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  20. 20
    Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E

    Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E por David Johnson, Shih‐hsin Kan, Michael Oldridge, Richard C. Trembath, Philippe Roche, Robert Esnouf, Henk Giele, Andrew O.M. Wilkie

    Publicado em 2003
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:

Ferramentas de busca: