Potentiation of the inductive effect of phenobarbital on cytochrome P450 mRNAs by cannabidiol von Deutsch, Dale G., Tombler, Eugene R., March, James E., Lo, Stephen H.C., Adesnik, Milton

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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Nutrients and suspended solids in dry weather and storm flows from a tropical catchment with various proportions of rural and urban land use von Chua, Lloyd H.C., Lo, Edmond Y.M., Shuy, E.B., Tan, Stephen B.K.

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Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong von 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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Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome von Tong, Tony M F, Hau, Edgar W L, Lo, Ivan F M, Chan, Daniel H C, Lam, Stephen T S

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Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T>A and 79G>T in RMRP gene von 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

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Prader–Willi Syndrome: 16-Year Experience in Hong Kong von 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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Oculopharyngeal muscular dystrophy: underdiagnosed disease in Hong Kong von Luk, HM, Lo, Ivan FM, Fu, KH, Lui, Colin HT, Tong, Tony MF, Chan, Daniel HC, Lam, Stephen TS

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