检索结果 - Andrew O.M. Wilkie

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  1. 1
    Craniosynostosis: genes and mechanisms

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

    出版 1997
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  2. 2
    The molecular basis of genetic dominance.

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

    出版 1994
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  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 由 Anne Goriely, Andrew O.M. Wilkie

    出版 2012
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  4. 4
    Craniosynostosis

    Craniosynostosis 由 David Johnson, Andrew O.M. Wilkie

    出版 2011
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  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 由 Gillian Morriss‐Kay, Andrew O.M. Wilkie

    出版 2005
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  6. 6
    A Genetic-Pathophysiological Framework for Craniosynostosis

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

    出版 2015
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  7. 7
    New insights into craniofacial malformations

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

    出版 2015
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  8. 8
    Cellular evidence for selfish spermatogonial selection in aged human testes

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

    出版 2013
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  9. 9
    Clinical genetics of craniosynostosis

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

    出版 2017
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  10. 10
    Functions of fibroblast growth factors and their receptors

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

    出版 1995
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  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 由 Jane Anderson, Helen D. Burns, Pita Enriquez-Harris, Andrew O.M. Wilkie, John K. Heath

    出版 1998
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  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 由 Anne Goriely, John J. McGrath, Christina M. Hultman, Andrew O.M. Wilkie, Dolores Malaspina

    出版 2013
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  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 由 Geoffrey J. Maher, Simon J. McGowan, Eleni Giannoulatou, Clare Verrill, Anne Goriely, Andrew O.M. Wilkie

    出版 2016
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  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 由 DR Higgs, Mark A. Vickers, Andrew O.M. Wilkie, IM Pretorius, Andrew P. Jarman, D. J. Weatherall

    出版 1989
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  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 由 DR Higgs, Mark A. Vickers, Andrew O.M. Wilkie, IM Pretorius, Andrew P. Jarman, D. J. Weatherall

    出版 1989
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  16. 16
    The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

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

    出版 1995
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  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 由 Lampros A. Mavrogiannis, Indira B. Taylor, Sally Davies, Feliciano J. Ramos, José L. Olivares, Andrew O.M. Wilkie

    出版 2005
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  18. 18
    Hearing loss in a mouse model of Muenke syndrome

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

    出版 2008
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  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 由 Dominic Furniss, Laura A. Lettice, Indira B. Taylor, Paul Critchley, Henk Giele, Robert E. Hill, Andrew O.M. Wilkie

    出版 2008
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  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 由 David Johnson, Shih‐hsin Kan, Michael Oldridge, Richard C. Trembath, Philippe Roche, Robert Esnouf, Henk Giele, Andrew O.M. Wilkie

    出版 2003
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