Prior education, life-contact and knowledge of autism amongst non-autistic students in higher education von Edwards, Steve, lyn bolton, Shen, Flinter, Angela, Thorpe, Kieran, Frost-Camilleri, Liam, Sawyer, Neroli, Kennedy, Gerard

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Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study von Ibañez, Kristina, Polke, James, Hagelstrom, R Tanner, Dolzhenko, Egor, Pasko, Dorota, Thomas, Ellen Rachel Amy, Smith, Katherine R, McDonagh, Ellen M, Polychronopoulos, Dimitris, Chan, Georgia, Davison, James E, Festenstein, Richard, Fratta, Pietro, Giunti, Paola, Howard, Robin, Venkata, Laxmi, Laurá, Matilde, Morris, Huw, Robinson, Robert, Rosser, Elisabeth, Faravelli, Francesca, Schrag, Anette, Schott, Jonathan M, Wood, Nicholas W, Bourn, David, Eggleton, Kelly, Twiss, Philip, Almheiri, Ghareesa, Sheikh, Isabella, Vandrovcova, Jana, Brittain, Helen, Baple, Emma, Moutsianas, Loukas, Deshpande, Viraj, Perry, Denise L, Ajay, Subramanian S., Rajan, Vani, Oprych, Kathryn, Chinnery, Patrick F, Wilson, Gill, Ellard, Sian, Temple, I Karen, McMullan, Dom, Naresh, Kikkeri, Flinter, Frances A, Taylor, Jenny C, Greenhalgh, Lynn, Newman, William, Brennan, Paul, Sayer, John A, Raymond, F Lucy, Deans, Zandra C, Hill, Sue, Fowler, Tom, Scott, Richard H, Chinnery, Patrick F, Rendon, Augusto, Eberle, Michael A, Taft, Ryan J, Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boissiere, Jeanne M., Devereau, Andrew, Elgar, Greg, Foulger, Rebecca E., Furió-Tarí, Pedro, Hackett, Joanne, Hamblin, Angela, Holman, James, Hubbard, Tim J.P., Jones, Louise J., Kayikci, Melis, Lawson, Kay, Leigh, Sarah E.A., Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Mueller, Michael, Murugaesu, Nirupa, Odhams, Chris A., Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Riesgo-Ferreiro, Pablo, Ryten, Mina, Savage, Kevin, Sawant, Kushmita, Sieghart, Alexander, Smedley, Damian, Sosinsky, Alona, Spooner, William, Stevens, Helen E., Stuckey, Alexander, Sultana, Razvan, Tregidgo, Carolyn, Walsh, Emma, Watters, Sarah A., Williams, Eleanor, Zarowiecki, Magdalena

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Germline selection shapes human mitochondrial DNA diversity von Wei, Wei, Tuna, Salih, Keogh, Michael J., Smith, Katherine R., Aitman, Timothy J., Beales, Phil L., Bennett, David L., Gale, Daniel P., Bitner-Glindzicz, Maria A. K., Black, Graeme C., Brennan, Paul, Elliott, Perry, Flinter, Frances A., Floto, R. Andres, Houlden, Henry, Irving, Melita, Koziell, Ania, Maher, Eamonn R., Markus, Hugh S., Morrell, Nicholas W., Newman, William G., Roberts, Irene, Sayer, John A., Smith, Kenneth G. C., Taylor, Jenny C., Watkins, Hugh, Webster, Andrew R., Wilkie, Andrew O. M., Williamson, Catherine, Ashford, Sofie, Penkett, Christopher J., Stirrups, Kathleen E., Rendon, Augusto, Ouwehand, Willem H., Bradley, John R., Raymond, F. Lucy, Caulfield, Mark, Turro, Ernest, Chinnery, Patrick F.

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Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort von Braddon, Fiona, Downward, Lewis, Coward, Richard J, Griffin, Sian, Hall, Matt, Karet Frankl, Fiona, Kerecuk, Larissa, Pinney, Jenny, Sayer, John A, Waters, Aoife, Bockenhauer, Detlef, Gale, Daniel P, Agbonmwandolor, Joy, Ahmad, Zubaidah, Asgari, Ellie, Ayers, Amanda, Barratt, Alison, Barratt, Jonathan, Benyon, Sarah, Bhandari, Sunil, Bond, Sally, Bramham, Kate, Branson, Angela, Byrne, Conor, Campbell, Gary, Capell, Alys, Cathcart, Tracy, Cheung, Chee Kay, Chick, Katy-Jane, Chrysochou, Tina, Clayton, Christopher, Cook, Wendy, Coward, Richard J, Drayson, Mark, Evans, Dawn, Flinter, Frances, Gale, Daniel P, Gallagher, Hugh, Game, David, Gavrila, Madita, Gilchrist, Mark, Goldsmith, Christopher, Gray, Barry, Griffith, Megan, Gupta, Sanjana, Hillman, Kate, Htet, Zay, Huish, Sharon, Hull, Richard, Hunter, Karl, Inston, Nick, Jayne, David, Jenkins, Alison, Kamesh, Lavanya, Kanigicherla, Durga, Karet Frankl, Fiona, Kaur, Amrit, King, Garry, King, Grant, Kislowska, Ewa, Kokocinska, Maria, Lawless, Laura, Mabillard, Holly, Mahdi, Khalid, Masoud, Sherry, Mayfair, Jake, Meyrick, Simon, Moochhala, Shabbir, Morgan, Ann, Muhammad, Fawad, Murray, Shona, Osmaston, Kate, Padmanabhan, Neal, Pattison, James, Persu, Alexandre, Petchey, William G, Post, Frank, Sandford, Richard, Sarween, Nadia, Sayer, John A, Sebire, Neil, Selvaskandan, Haresh, Sharma, Asheesh, Sheerin, Neil, Shetty, Harish, Simms, Roslyn, Smith, Kerry, Swift, Pauline, Szklarzewicz, Justyna, Tam, Fred, Tan, Kay, Tischkowitz, Marc, Tse, Yincent, Tyerman, Kay, Usher, Miranda, Wechalekar, Ashutosh, Welsh, Gavin I, West, Nicol, Williams, Angharad, Wilson, Patricia D

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Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders von Wolfe, Kate, Strydom, André, Morrogh, Deborah, Carter, Jennifer, Cutajar, Peter, Eyeoyibo, Mo, Hassiotis, Angela, McCarthy, Jane, Mukherjee, Raja, Paschos, Dimitrios, Perumal, Nagarajan, Read, Stephen, Shankar, Rohit, Sharif, Saif, Thirulokachandran, Suchithra, Thygesen, Johan H, Patch, Christine, Ogilvie, Caroline, Flinter, Frances, McQuillin, Andrew, Bass, Nick

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Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort von Braddon, Fiona, Downward, Lewis, Hall, Matt, Kerecuk, Larissa, Sayer, John A., Sinha, Smeeta, Srivastava, Shalabh, Tam, Frederick W.K., Waters, Aoife, Wong, Edwin, Huang, Kui, Ye, Jamie, Nitsch, Dorothea, Saleem, Moin, Almasarwah, Rashid, Annear, Nicholas, Balasubramaniam, Gowrie, Bansal, Tarun, Barratt, Jonathan, Bendle, Janet, Bhandari, Sunil, Bramham, Kate, Brocklebank, Vicky, Cairns, Hugh, Chess, James, Chitalia, Nihil, Chrysochou, Tina, Clark, Katherine, Clayton, Christopher, Clissold, Rhian, Colclough, Viv, Conway, Eileen, Cook, H. Terence, Crosbie, Sarah, Cserep, Gabor, Davidson, Katherine, Dixit, Abhijit, Drayson, Mark, Dreyer, Gavin, Francis, Lucy, Gallagher, Hugh, Gear, Susie, Goggolidou, Paraskevi, Gooden, Patricia, Grammatikopoulos, Tassos, Griffith, Megan, Gumus, Steph, Harris, Tess, Haskell, Louise, Hiremath, Mrityunjay, Htet, Zay, Inston, Nick, Jenfa, Gbemisola, Jones, Colin, Kanigicherla, Durga, Karim, Mahzuz, King, Garry, King, Grant, Klata, Edyta, Ledson, Thomas, Lennon, Rachel, Maggie Lai, Ling Wai, Lovitt, Graham, Lyons, Paul, Mahdi, Khalid, Mark, Patrick B., Mckinnell, Joanna, Moochhala, Shabbir, Morgan, Ann, Murray, Shona, Ong, Albert CM, Osmaston, Kate, Padmanabhan, Neal, Paul, Riny, Perkins, Stephen J., Petchey, William G., Pickering, Matthew C., Plummer, Zoe, Power, Albert, Pusey, Charles, Rabara, Ria, Raju, Tina, Rumjon, Adam, Sandford, R.N., Sayer, John A., Shah, Sapna, Sinha, Manish, Srivastava, Shalabh, Stott, Ian, Stroud, Katerina, Taylor, Robert, Turnbull, Alison, Walsh, Stephen B., Wechalekar, Ashutosh, Wiles, Kate, Willcocks, Lisa, Williams, Angharad, Williams, Karen, Wood, Grahame, Woodward, Emma

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The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993 von Vetrie, David, Vořechovský, Igor, Sideras, Paschalis, Holland, Jill, Davies, Angela, Flinter, Frances, Hammarström, Lennart, Kinnon, Christine, Levinsky, Roland, Bobrow, Martin, Smith, C I Edvard, Bentley, David R

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Delineation of two distinct 6p deletion syndromes von DAVIES, A. F, MIRZA, G, RAGOUSSIS, J, SEKHON, G, TURNPENNY, P, LEROY, F, SPELEMAN, F, LAW, C, VAN REGEMORTER, N, VAMOS, E, FLINTER, F

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An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2α that affects anterior eye chamber development von DAVIES, A. F, MIRZA, G, FLINTER, F, RAGOUSSIS, J

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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases von VETRIE, D, VORECHOVSKY, I, SMITH, C. I. E, BENTLEY, D. R, SIDERAS, P, HOLLAND, J, DAVIES, A, FLINTER, F, HAMMARSTRÖM, L, KINNON, C, LEVINSKY, R, BOBROW, M

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Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region von F.Davles, Angela, J.Stephens, Richard, G.OIavesen, Mark, Heather, Lisa, J.Dixon, Michael, Magee, Alex, Flinter, Frances, Ragoussis, Jiannis

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A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome von Davies, A F, Olavesen, M G, Stephens, R J, Davidson, R, Delneste, D, Van Regemorter, N, Vamos, E, Flinter, F, Abusaad, I, Ragoussis, J

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An interstitial deletion of 6p24-p25 proximal to theFKHL7 locus and includingAP-2α that affects anterior eye chamber development von Davies, Angela F, Mirza, Ghazala, Flinter, Frances, Ragoussis, Jiannis

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An interstitial deletion of 6p24-p25 proximal to theFKHL7 locus and includingAP-2[alpha] that affects anterior eye chamber development von Davies, Angela F, Mirza, Ghazala, Flinter, Frances, Ragoussis, Jiannis

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Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome? von McKee, S A, Barnicoat, A, Fryer, A, Flinter, F, McCormick, D, McKeown, C

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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases von Vetrie, David, Vořechovský, Igor, Sideras, Paschalis, Holland, Jill, Davies, Angela, Flinter, Frances, Hammarström, Lennart, Kinnon, Christine, Levinsky, Roland, Bobrow, Martin, Smith, C. I. Edvard, Bentley, David R.

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