Search Results - Ling-Fung Tang, P

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  1. 1
    Two missense mutations in SALL4 in a patient with microphthalmia, coloboma, and optic nerve hypoplasia

    Two missense mutations in SALL4 in a patient with microphthalmia, coloboma, and optic nerve hypoplasia by Ullah, E, Wu, D, Madireddy, L, Lao, R, Ling-Fung Tang, P, Wan, E, Bardakjian, T, Kopinsky, S, Kwok, P-Y, Schneider, A, Baranzini, S, Ansar, M, Slavotinek, A

    Published in Ophthalmic genetics
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  2. 2
    Two missense mutations in SALL4 in a patient with microphthalmia, coloboma, and optic nerve hypoplasia

    Two missense mutations in SALL4 in a patient with microphthalmia, coloboma, and optic nerve hypoplasia by Ullah, E., Wu, D., Madireddy, L., Lao, R., Ling-Fung Tang, P., Wan, E., Bardakjian, T., Kopinsky, S., Kwok, P.-Y., Schneider, A., Baranzini, S., Ansar, M., Slavotinek, A.

    Published in Ophthalmic Genetics
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  3. 3
    An internal promoter underlies the difference in disease severity between N- and C-terminal truncation mutations of Titin in zebrafish

    An internal promoter underlies the difference in disease severity between N- and C-terminal truncation mutations of Titin in zebrafish by Zou, Jun, Tran, Diana, Baalbaki, Mai, Tang, Ling Fung, Poon, Annie, Pelonero, Angelo, Titus, Erron W, Yuan, Christiana, Shi, Chenxu, Patchava, Shruthi, Halper, Elizabeth, Garg, Jasmine, Movsesyan, Irina, Yin, Chaoying, Wu, Roland, Wilsbacher, Lisa D, Liu, Jiandong, Hager, Ronald L, Coughlin, Shaun R, Jinek, Martin, Pullinger, Clive R, Kane, John P, Hart, Daniel O, Kwok, Pui-Yan, Deo, Rahul C

    Published in eLife
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  4. 4
    Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1

    Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1 by Slavotinek, A. M., Mehrotra, P., Nazarenko, I., Tang, P. L.-F., Lao, R., Cameron, D., Li, B., Chu, C., Chou, C., Marqueling, A. L., Yahyavi, M., Cordoro, K., Frieden, I., Glaser, T., Prescott, T., Morren, M.-A., Devriendt, K., Kwok, P.-y., Petkovich, M., Desnick, R. J.

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  5. 5
    A polymorphism in TLR2 is associated with arterial thrombosis in a multiethnic population of patients with systemic lupus erythematosus

    A polymorphism in TLR2 is associated with arterial thrombosis in a multiethnic population of patients with systemic lupus erythematosus by Kaiser, Rachel, Tang, Ling Fung, Taylor, Kimberly E, Sterba, Kirsten, Nititham, Joanne, Brown, Elizabeth E, Edberg, Jeffrey C, McGwin, Jr, Gerald, Alarcón, Graciela S, Ramsey-Goldman, Rosalind, Reveille, John D, Vilá, Luis M, Petri, Michelle, Rauch, Joyce, Miller, Emily, Mesznik, Kara, Kwok, Pui-Yan, Kimberly, Robert P, Salmon, Jane E, Criswell, Lindsey A

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  6. 6
    Brief Report: A Polymorphism in TLR2 Is Associated With Arterial Thrombosis in a Multiethnic Population of Patients With Systemic Lupus Erythematosus

    Brief Report: A Polymorphism in TLR2 Is Associated With Arterial Thrombosis in a Multiethnic Population of Patients With Systemic Lupus Erythematosus by Kaiser, Rachel, Tang, Ling Fung, Taylor, Kimberly E., Sterba, Kirsten, Nititham, Joanne, Brown, Elizabeth E., Edberg, Jeffrey C., McGwin, Gerald, Alarcón, Graciela S., Ramsey‐Goldman, Rosalind, Reveille, John D., Vilá, Luis M., Petri, Michelle, Rauch, Joyce, Miller, Emily, Mesznik, Kara, Kwok, Pui‐Yan, Kimberly, Robert P., Salmon, Jane E., Criswell, Lindsey A.

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