Cannabis use frequency and pain interference among people with HIV
Klepp, T. D., Heeren, T. C., Winter, M. R., Lloyd-Travaglini, C. A., Magane, K. M., Romero-Rodríguez, E., Kim, T. W., Walley, A. Y., Mason, T., Saitz, R.
Published in AIDS care (03.08.2023)
Published in AIDS care (03.08.2023)
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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study
Ryan, A K, Goodship, J A, Wilson, D I, Philip, N, Levy, A, Seidel, H, Schuffenhauer, S, Oechsler, H, Belohradsky, B, Prieur, M, Aurias, A, Raymond, F L, Clayton-Smith, J, Hatchwell, E, McKeown, C, Beemer, F A, Dallapiccola, B, Novelli, G, Hurst, J A, Ignatius, J, Green, A J, Winter, R M, Brueton, L, Brøndum-Nielsen, K, Scambler, P J
Published in Journal of medical genetics (01.10.1997)
Published in Journal of medical genetics (01.10.1997)
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Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
de Vries, B B A, White, S M, Knight, S J L, Regan, R, Homfray, T, Young, I D, Super, M, McKeown, C, Splitt, M, Quarrell, O W J, Trainer, A H, Niermeijer, M F, Malcolm, S, Flint, J, Hurst, J A, Winter, R M
Published in Journal of medical genetics (01.03.2001)
Published in Journal of medical genetics (01.03.2001)
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Journal Article
Subtle chromosomal rearrangements in children with unexplained mental retardation
Knight, Samantha JL, Regan, Regina, Nicod, Alison, Horsley, Sharon W, Kearney, Lyndal, Homfray, Tessa, Winter, Robin M, Bolton, Patrick, Flint, Jonathan
Published in The Lancet (British edition) (13.11.1999)
Published in The Lancet (British edition) (13.11.1999)
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Journal Article
Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype
Ryan, A K, Bartlett, K, Clayton, P, Eaton, S, Mills, L, Donnai, D, Winter, R M, Burn, J
Published in Journal of medical genetics (01.07.1998)
Published in Journal of medical genetics (01.07.1998)
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Journal Article
Synpolydactyly Phenotypes Correlate with Size of Expansions in HOXD13 Polyalanine Tract
Goodman, F. R., Mundlos, S., Muragaki, Y., Donnai, D., Giovannucci-Uzielli, M. L., Lapi, E., Majewski, F., McGaughran, J., McKeown, C., Reardon, W., Upton, J., Winter, R. M., Olsen, B. R., Scambler, P. J.
Published in Proceedings of the National Academy of Sciences - PNAS (08.07.1997)
Published in Proceedings of the National Academy of Sciences - PNAS (08.07.1997)
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European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities
Feenstra, I., Fang, J., Koolen, D.A., Siezen, A., Evans, C., Winter, R.M., Lees, M.M., Riegel, M., de Vries, B.B.A., Van Ravenswaaij, C.M.A., Schinzel, A.
Published in European journal of medical genetics (01.07.2006)
Published in European journal of medical genetics (01.07.2006)
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Journal Article
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
Reardon, William, Winter, Robin M, Rutland, Paul, Pulleyn, Louise J, Jones, Barry M, Malcolm, Sue
Published in Nature genetics (01.09.1994)
Published in Nature genetics (01.09.1994)
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Journal Article
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis
Superti-Furga, Andrea, Shears, Deborah J, Reardon, William, Palmer, Rodger W, Vassal, Humberto J, Scambler, Peter J, Winter, Robin M, Goodman, Frances R
Published in Nature genetics (01.05.1998)
Published in Nature genetics (01.05.1998)
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Journal Article
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
Muenke, Maximilian, Schell, Ute, Hehr, Andreas, Robin, Nathaniel H, Losken, H. Wolfgang, Schinzel, Albert, Pulleyn, Louise J, Rutland, Paul, Reardon, William, Malcolm, Sue, Winter, Robin M
Published in Nature genetics (01.11.1994)
Published in Nature genetics (01.11.1994)
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Journal Article
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
Plenge, Robert M, Hendrich, Brian D, Schwartz, Charles, Arena, J. Fernando, Naumova, Anna, Sapienza, Carmen, Winter, Robin M, Willard, Huntington F
Published in Nature genetics (01.11.1997)
Published in Nature genetics (01.11.1997)
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Journal Article
Medication for addiction treatment and acute care utilization in HIV-positive adults with substance use disorders
Thakarar, K., Walley, A. Y., Heeren, T. C., Winter, M. R., Ventura, A. S., Sullivan, M., Drainoni, M., Saitz, R.
Published in AIDS care (01.09.2020)
Published in AIDS care (01.09.2020)
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Journal Article
Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literature
Rossi, M, Guerrini, R, Dobyns, W B, Andria, G, Winter, R M
Published in Neuropediatrics (01.12.2003)
Published in Neuropediatrics (01.12.2003)
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Journal Article
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
KELBERMAN, D, TYSON, J, HAAN, E. A, LAING, N. G, LIM, J, MALCOLM, S, SINGER, S. L, WINTER, R. M, BITNER-GLINDZICZ, M, CHANDLER, D. C, MCINERNEY, A. M, SLEE, J, ALBERT, D, AYMAT, A, BOTMA, M, CALVERT, M, GOLDBLATT, J
Published in Human genetics (01.12.2001)
Published in Human genetics (01.12.2001)
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Journal Article
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
Rutland, Paul, Pulleyn, Louise J, Reardon, William, Baraitser, Michael, Hayward, Richard, Jones, Barry, Malcolm, Sue, Winter, Robin M, Oldridge, Michael, Slaney, Sarah F, Poole, Michael D, Wilkie, Andrew O.M
Published in Nature genetics (01.02.1995)
Published in Nature genetics (01.02.1995)
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Journal Article
The Twist Gene, Although Not Disrupted In Saethre-Chotzen Patients With Apparently Balanced Translocations of 7p21, Is Mutated In Familial and Sporadic Cases
Rose, C.S. P., Patel, P., Reardon, W., Malcolm, S., Winter, R. M.
Published in Human molecular genetics (01.08.1997)
Published in Human molecular genetics (01.08.1997)
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