Search Results - Tong, Tony M.F.

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  1. 1
    Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA)

    Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA) by Lai, Kent K.S., Lo, Ivan F.M., Tong, Tony M.F., Cheng, Lydia Y.L., Lam, Stephen T.S.

    Published in Clinical biochemistry
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  2. 2
    Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong

    Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong by Yu, Kris P. T., Luk, Ho‐Ming, Leung, Gordon K. C., Mak, Christopher C. Y., Cheng, Shirley S. W., Hau, Edgar W. L., Chan, David K. H., Lam, Stephen T. S., Tong, Tony M. F., Chung, Brian H. Y., Lo, Ivan F. M.

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  3. 3
    Prader–Willi Syndrome: 16-Year Experience in Hong Kong

    Prader–Willi Syndrome: 16-Year Experience in Hong Kong by Lo, Ivan F.M., Luk, Ho Ming, Tong, Tony M.F., Lai, Kent K.S., Chan, Daniel H.C., Lam, Albert C.F., Chan, David K.H., Hau, Edgar W.L., Fung, Connie O.Y., Lam, Stephen T.S.

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  4. 4
    Silver-Russell syndrome in Hong Kong

    Silver-Russell syndrome in Hong Kong by Luk, H M, Yeung, K S, Wong, W L, Chung, B Hy, Tong, T Mf, Lo, I Fm

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  5. 5
    Birt-Hogg-Dubé syndrome: a rare cause of familial spontaneous pneumothorax

    Birt-Hogg-Dubé syndrome: a rare cause of familial spontaneous pneumothorax by Luk, H M, Tong, T Mf, Lo, I Fm

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  6. 6
    The nail points to the diagnosis

    The nail points to the diagnosis by Tong, Stephanie YK, Luk, HM, Tong, Tony MF, Lo, Ivan FM

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  7. 7
    A young woman with mucocutaneous pigmentation and intestinal polyps

    A young woman with mucocutaneous pigmentation and intestinal polyps by Luk, H M, Lo, Ivan F M, Yu, Kelvin M C, Tong, Tony M F, Lam, Stephen T S

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  8. 8
    Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong

    Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong by Luk, H M, Lo, Ivan F M, Lai, Carmen W S, Ma, Louis C K, Tong, Tony M F, Chan, Daniel H C, Lam, Stephen T S

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  9. 9
    High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardation

    High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardation by Lam, Albert C.F., Lam, Stephen T.S., Lai, Kent K.S., Tong, Tony M.F., Chau, T.C.

    Published in Clinical biochemistry
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  10. 10
    Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T>A and 79G>T in RMRP gene

    Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T>A and 79G>T in RMRP gene by LAM, Albert C. F, CHAN, Daniel H. C, TONG, Tony M. F, TANG, Mary H. Y, LO, Steven Y. F, LO, Ivan F. M, LAM, Stephen T. S

    Published in Prenatal diagnosis
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  11. 11
    Oculopharyngeal muscular dystrophy: underdiagnosed disease in Hong Kong

    Oculopharyngeal muscular dystrophy: underdiagnosed disease in Hong Kong by Luk, HM, Lo, Ivan FM, Fu, KH, Lui, Colin HT, Tong, Tony MF, Chan, Daniel HC, Lam, Stephen TS

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