Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome von Woods, C.G., Stricker, S., Seemann, P., Stern, R., Cox, J., Sherridan, E., Roberts, E., Springell, K., Scott, S., Karbani, G., Sharif, S.M., Toomes, C., Bond, J., Kumar, D., Al-Gazali, L., Mundlos, S.

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Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation von Roberts, E, Hampshire, D J, Pattison, L, Springell, K, Jafri, H, Corry, P, Mannon, J, Rashid, Y, Crow, Y, Bond, J, Woods, C G

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Microcephaly von Woods, C.G., Basto, R.

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Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis von James, Jacqueline, Davies, Robin, Read, Andrew P, Roberts, Emma, Woods, C. Geoffrey, Wood, A. Joseph, McCormick, Derek, Hewitt, Chelsee, Ghaffar, Khaled Abdul, Thakker, Nalin S, Widmer, Richard, Wong, Melanie, Sloan, Philip, Lench, Nicholas, Hussein, Ibtessam Ramzy, Pemberton, Michael, Dixon, Michael J, Markham, Alexander, Temtamy, Samia A, Wu, Chu Lee, Toomes, Carmel, Moynihan, Leanne

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Autosomal Recessive Primary Microcephaly (MCPH): A Review of Clinical, Molecular, and Evolutionary Findings von Woods, C. Geoffrey, Bond, Jacquelyn, Enard, Wolfgang

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Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36 von Hampshire, Daniel J, Roberts, Emma, Crow, Yanick, Bond, Jacquelyn, Mubaidin, Ammar, Wriekat, Abdul-Latif, Al-Din, Amir, Woods, C Geoffrey

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Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum von Mubaidin, A, Roberts, E, Hampshire, D, Dehyyat, M, Shurbaji, A, Mubaidien, M, Jamil, A, Al-Din, A, Kurdi, A, Woods, C G

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A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy von Carvalho, Ofélia P, Thornton, Gemma K, Hertecant, Joseph, Houlden, Henry, Nicholas, Adeline K, Cox, James J, Rielly, Mary, Al-Gazali, Lihadh, Woods, C Geoffrey

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A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome von Jeggo, Penny A, O'Driscoll, Mark, Ruiz-Perez, Victor L, Woods, C. Geoffrey, Goodship, Judith A

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ASPM is a major determinant of cerebral cortical size von Woods, C. Geoffrey, Bond, Jacquelyn, Roberts, Emma, Mochida, Ganesh H, Hampshire, Daniel J, Scott, Sheila, Askham, Jonathan M, Springell, Kelly, Mahadevan, Meera, Crow, Yanick J, Markham, Alexander F, Walsh, Christopher A

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Congenital glaucoma and brain stem atrophy as features of Aicardi–Goutières syndrome von Crow, Yanick J., Massey, R.F., Innes, J.R., Pairaudeau, P.W., Rowland Hill, C.A., Woods, C.G., Ali, M., Livingston, J.H., Lebon, P., Nischall, K., McEntagart, M., Hindocha, N., Winter, R.M.

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Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter von Jackson, Andrew P., McHale, Duncan P., Campbell, David A., Jafri, Hussain, Rashid, Yasmin, Mannan, Jovaria, Karbani, Gulshan, Corry, Peter, Levene, Malcolm I., Mueller, Robert F., Markham, Alexander F., Lench, Nicholas J., Woods, C. Geoffrey

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A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34 von Moynihan, Leanne, Jackson, Andrew P., Roberts, Emma, Karbani, Gulshan, Lewis, Ian, Corry, Peter, Turner, Gwen, Mueller, Robert F., Lench, Nicholas J., Woods, C. Geoffrey

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Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome von Celli, Jacopo, Duijf, Pascal, Hamel, Ben C.J, Bamshad, Michael, Kramer, Bridget, Smits, Arie P.T, Newbury-Ecob, Ruth, Hennekam, Raoul C.M, Van Buggenhout, Griet, van Haeringen, Arie, Woods, C.Geoffrey, van Essen, Anthonie J, de Waal, Rob, Vriend, Gert, Haber, Daniel A, Yang, Annie, McKeon, Frank, Brunner, Han G, van Bokhoven, Hans

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A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25 von McHale, D.P., Mitchell, S., Bundey, S., Moynihan, L., Campbell, D.A., Woods, C.G., Lench, N.J., Mueller, R.F., Markham, A.F.

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Investigating microcephaly von Woods, C Geoffrey, Parker, Alasdair

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Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16 von Chandler, K. E., Del Rio, A., Rakshi, K., Springell, K., Williams, D. K., Stoodley, N., Woods, C. G., Pilz, D. T.

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DNA repair disorders von Woods, C Geoffrey

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Asymmetry and skin pigmentary anomalies in chromosome mosaicism von Woods, C G, Bankier, A, Curry, J, Sheffield, L J, Slaney, S F, Smith, K, Voullaire, L, Wellesley, D

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Painful and painless channelopathies von Bennett, David L H, Dr, Woods, C Geoffrey, Prof

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