Publisher Correction: Deterministic delivery of remote entanglement on a quantum network
Humphreys, Peter C., Kalb, Norbert, Morits, Jaco P. J., Schouten, Raymond N., Vermeulen, Raymond F. L., Twitchen, Daniel J., Markham, Matthew, Hanson, Ronald
Published in Nature (London) (01.10.2018)
Published in Nature (London) (01.10.2018)
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Deployed measurement-device independent quantum key distribution and Bell-state measurements coexisting with standard internet data and networking equipment
Berrevoets, Remon C., Middelburg, Thomas, Vermeulen, Raymond F. L., Chiesa, Luca Della, Broggi, Federico, Piciaccia, Stefano, Pluis, Rene, Umesh, Prathwiraj, Marques, Jorge F., Tittel, Wolfgang, Slater, Joshua A.
Published in Communications physics (16.07.2022)
Published in Communications physics (16.07.2022)
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Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
Riazuddin, S., Hussain, M., Razzaq, A., Iqbal, Z., Shahzad, M., Polla, D. L., Song, Y., van Beusekom, E., Khan, A. A., Tomas-Roca, L., Rashid, M., Zahoor, M. Y., Wissink-Lindhout, W. M., Basra, M. A. R., Ansar, M., Agha, Z., van Heeswijk, K., Rasheed, F., Van de Vorst, M., Veltman, J. A., Gilissen, C., Akram, J., Kleefstra, T., Assir, M. Z., Grozeva, D., Carss, K., Raymond, F. L., O’Connor, T. D., Riazuddin, S. A., Khan, S. N., Ahmed, Z. M., de Brouwer, A. P. M., van Bokhoven, H., Riazuddin, S.
Published in Molecular psychiatry (01.11.2020)
Published in Molecular psychiatry (01.11.2020)
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Functional Analyses of a Novel Splice Variant in the CHD7 Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome
Villate, Olatz, Ibarluzea, Nekane, Fraile-Bethencourt, Eugenia, Valenzuela, Alberto, Velasco, Eladio A, Grozeva, Detelina, Raymond, F L, Botella, María P, Tejada, María-Isabel
Published in Frontiers in genetics (26.01.2018)
Published in Frontiers in genetics (26.01.2018)
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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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Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
Riazuddin, S, Hussain, M, Razzaq, A, Iqbal, Z, Shahzad, M, Polla, D L, Song, Y, van Beusekom, E, Khan, A A, Tomas-Roca, L, Rashid, M, Zahoor, M Y, Wissink-Lindhout, W M, Basra, M A R, Ansar, M, Agha, Z, van Heeswijk, K, Rasheed, F, Van de Vorst, M, Veltman, J A, Gilissen, C, Akram, J, Kleefstra, T, Assir, M Z, Grozeva, D, Carss, K, Raymond, F L, O'Connor, T D, Riazuddin, S A, Khan, S N, Ahmed, Z M, de Brouwer, A P M, van Bokhoven, H, Riazuddin, S
Published in Molecular psychiatry (01.11.2017)
Published in Molecular psychiatry (01.11.2017)
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Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation
Field, M, Tarpey, P, Boyle, J, Edkins, S, Goodship, J, Luo, Y, Moon, J, Teague, J, Stratton, MR, Futreal, PA, Wooster, R, Raymond, FL, Turner, G
Published in Clinical genetics (01.12.2006)
Published in Clinical genetics (01.12.2006)
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Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification
Douglas, J, Tatton-Brown, K, Coleman, K, Guerrero, S, Berg, J, Cole, T R P, FitzPatrick, D, Gillerot, Y, Hughes, H E, Pilz, D, Raymond, F L, Temple, I K, Irrthum, A, Schouten, J P, Rahman, N
Published in Journal of medical genetics (01.09.2005)
Published in Journal of medical genetics (01.09.2005)
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Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutation
Turner, G, Boyle, J, Partington, MW, Kerr, B, Raymond, FL, Gécz, J
Published in Clinical genetics (01.02.2008)
Published in Clinical genetics (01.02.2008)
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Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder
Chaudhry, A., Noor, A., Degagne, B., Baker, K., Bok, L. A., Brady, A. F., Chitayat, D., Chung, B. H., Cytrynbaum, C., Dyment, D., Filges, I., Helm, B., Hutchison, H. T., Jeng, L. J. B., Laumonnier, F., Marshall, C. R., Menzel, M., Parkash, S., Parker, M. J., Raymond, L. F., Rideout, A. L., Roberts, W., Rupps, R., Schanze, I., Schrander-Stumpel, C. T. R. M., Speevak, M. D., Stavropoulos, D. J., Stevens, S. J. C., Thomas, E. R. A., Toutain, A., Vergano, S., Weksberg, R., Scherer, S. W., Vincent, J. B., Carter, M. T.
Published in Clinical genetics (01.09.2015)
Published in Clinical genetics (01.09.2015)
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The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene
Schwartz, Charles E, Tarpey, Patrick S, Lubs, Herbert A, Verloes, Alain, May, Melanie M, Risheg, Hiba, Friez, Michael J, Futreal, P Andrew, Edkins, Sarah, Teague, Jon, Briault, Sylvain, Skinner, Cindy, Bauer-Carlin, Astrid, Simensen, Richard J, Joseph, Sumy M, Jones, Julie R, Gecz, Josef, Stratton, Michael R, Raymond, F Lucy, Stevenson, Roger E
Published in Journal of medical genetics (01.07.2007)
Published in Journal of medical genetics (01.07.2007)
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Neurofibromatosis 2 in a patient with a de novo balanced reciprocal translocation 46,X,t(X;22)(p11.2;q11.2)
Bovie, C, Holden, S T, Schroer, A, Smith, E, Trump, D, Raymond, F L
Published in Journal of medical genetics (01.09.2003)
Published in Journal of medical genetics (01.09.2003)
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Fetal echocardiography as a predictor of chromosomal abnormality
Raymond, FL, Simpson, JM, Sharland, GK, Ogilvie, CM Mackie
Published in The Lancet (British edition) (27.09.1997)
Published in The Lancet (British edition) (27.09.1997)
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