Search Results - MCMULLAN, Tristan F. W

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  1. 1
    Upper Eyelid Myectomy in Blepharospasm with Associated Apraxia of Lid Opening

    Upper Eyelid Myectomy in Blepharospasm with Associated Apraxia of Lid Opening by Georgescu, Dan, Vagefi, M. Reza, McMullan, Tristan F.W, McCann, John D, Anderson, Richard L

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  2. 2
    Novel mutation in the RNASEH1 gene in a chronic progressive external ophthalmoplegia patient

    Novel mutation in the RNASEH1 gene in a chronic progressive external ophthalmoplegia patient by Sachdev, Anshu, Fratter, Carl, McMullan, Tristan F.W.

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  3. 3
    Stereolithographic models to guide orbital and oculoplastic surgery

    Stereolithographic models to guide orbital and oculoplastic surgery by Beigi, Bijan, McMullan, Tristan F. W., Gupta, Deepak, Khandwala, Mona

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  4. 4
    Autologous dermis graft at the time of evisceration or enucleation

    Autologous dermis graft at the time of evisceration or enucleation by Vagefi, M Reza, McMullan, Tristan F W, Burroughs, John R, Isaacs, David K, Tsirbas, Angelo, White, George L, Anderson, Richard L, McCann, John D

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  5. 5
    Towards an Understanding of Congenital Ptosis

    Towards an Understanding of Congenital Ptosis by McMullan, Tristan F. W., Robinson, David O., Tyers, Anthony G.

    Published in Orbit (Amsterdam)
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  6. 6
    A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation

    A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation by MCMULLAN, Tristan F. W, CROLLA, John A, GREGORY, Simon G, CARTER, Nigel P, COOPER, Rachel A, HOWELL, Gareth R, ROBINSON, David O

    Published in Human genetics
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  7. 7
    A Novel X-Linked Dominant Condition: X-Linked Congenital Isolated Ptosis

    A Novel X-Linked Dominant Condition: X-Linked Congenital Isolated Ptosis by McMullan, Tristan F.W., Collins, Andrew R., Tyers, Anthony G., Robinson, David O.

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  8. 8
    X-Linked Dominant Congenital Ptosis Cosegregating with an Interstitial Insertion of a Chromosome 1p21.3 Fragment into a Quasipalindromic Sequence in Xq27.1

    X-Linked Dominant Congenital Ptosis Cosegregating with an Interstitial Insertion of a Chromosome 1p21.3 Fragment into a Quasipalindromic Sequence in Xq27.1 by Bunyan, David J., Robinson, David O., Tyers, Anthony G., Huang, Shuwen, Maloney, Vivienne K., Grand, Francis H., Ennis, Sarah, Silva, Samantha R. de, Crolla, John A., McMullan, Tristan F. W.

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  9. 9
    Preoperative Assessment of the Eye and Periocular Region

    Preoperative Assessment of the Eye and Periocular Region by Burroughs, John R, Anderson, Richard L, Patrinely, James R, Weinberg, David A, McCann, John D, McMullan, Tristan F.W.

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  10. 10
    Novel mutation in the RNASEH1 gene in a chronic progressive external ophthalmoplegia patient

    Novel mutation in the RNASEH1 gene in a chronic progressive external ophthalmoplegia patient by Sachdev, Anshu, Fratter, Carl, McMullan, Tristan F W

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