Treffer 1 - 20 von 30 für Suche 'Berry, Chandler J', Suchdauer: 1,29s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4

    Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

    Veröffentlicht in The Lancet (British edition)

    Volltext
    Artikel
  5. 5

    Many Labs 2: Investigating Variation in Replicability Across Samples and Settings von Klein, Richard A., Vianello, Michelangelo, Hasselman, Fred, Adams, Byron G., Babalola, Mayowa T., Bahník, Štěpán, Batra, Rishtee, Berkics, Mihály, Bernstein, Michael J., Binan, Evans Dami, Bocian, Konrad, Busching, Robert, Cai, Huajian, Cambier, Fanny, Cantarero, Katarzyna, Carmichael, Cheryl L., Ceric, Francisco, Chen, Eva E., Cheong, Winnee, Coleman, Jennifer A., Conway, Morgan A., Curran, Paul G., Davis, William E., de Bruijn, Maaike, de Vries, Marieke, Dozo, Nerisa, Dunham, Yarrow, Durrheim, Kevin, Eller, Anja, Finck, Carolyn, Freyre, Miguel-Ángel, Friedman, Mike, Galliani, Elisa Maria, Gandi, Joshua C., Giessner, Steffen R., Gill, Tripat, Grahe, Jon E., Grahek, Ivan, Green, Eva G. T., Haigh, Matthew, Haines, Elizabeth L., Hall, Michael P., Hicks, Joshua A., Huntsinger, Jeffrey R., Huynh, Ho Phi, Inbar, Yoel, Innes-Ker, Åse H., Jiménez-Leal, William, Joy-Gaba, Jennifer A., Kappes, Heather Barry, Karick, Haruna, Keller, Victor N., Kervyn, Nicolas, Knežević, Goran, Krueger, Lacy E., Lazarević, Ljiljana B., Levitan, Carmel A., Lewis, Neil A., Lins, Samuel, Lipsey, Nikolette P., Losee, Joy E., Mallett, Robyn K., Marotta, Satia A., Mena-Pacheco, Fernando, Morris, Wendy L., Murphy, Sean C., Myachykov, Andriy, Neijenhuijs, Koen, Nelson, Anthony J., Lee Nichols, Austin, O’Donnell, Susan L., Oikawa, Haruka, Ong, Elsie, Packard, Grant, Pérez-Sánchez, Rolando, Podesta, Lysandra, Pollmann, Monique M. H., Rutchick, Abraham M., Saeri, Alexander K., Schmidt, Kathleen, Schönbrodt, Felix D., Smith-Castro, Vanessa, Steiner, Troy G., Stouten, Jeroen, Street, Chris N. H., Tang, Andrew C. W., Tanzer, Norbert, Tear, Morgan J., Traczyk, Jakub, Ujhelyi, Adrienn, van Aert, Robbie C. M., van der Hulst, Marije, Ann Vaughn, Leigh, Verniers, Catherine, Verschoor, Mark, Welch, Cheryl, Wood, Michael, Woodzicka, Julie A., Zhijia, Zeng, Nosek, Brian A.


    Volltext
    Artikel
  6. 6
  7. 7

    Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients von Santen, Gijs W.E., Aten, Emmelien, Vulto-van Silfhout, Anneke T., Pottinger, Caroline, van Bon, Bregje W.M., van Minderhout, Ivonne J.H.M., Snowdowne, Ronelle, van der Lans, Christian A.C., Boogaard, Merel, Linssen, Margot M.L., Vijfhuizen, Linda, van der Wielen, Michiel J.R., Vollebregt, M.J. (Ellen), Breuning, Martijn H., Kriek, Marjolein, van Haeringen, Arie, den Dunnen, Johan T., Hoischen, Alexander, Clayton-Smith, Jill, de Vries, Bert B.A., Hennekam, Raoul C.M., van Belzen, Martine J., Almureikhi, Mariam, Baban, Anwar, Barbosa, Mafalda, Ben-Omran, Tawfeg, Berry, Katherine, Bigoni, Stefania, Boute, Odile, Brueton, Louise, van der Burgt, Ineke, Canham, Natalie, Chandler, Kate E., Chrzanowska, Krystyna, Collins, Amanda L., de Toni, Teresa, Dean, John, den Hollander, Nicolette S., Flore, Leigh Anne, Fryer, Alan, Gardham, Alice, Graham Jr, John M., Harrison, Victoria, Horn, Denise, Jongmans, Marjolijn C., Josifova, Dragana, Kant, Sarina G., Kapoor, Seema, Kingston, Helen, Kini, Usha, Kleefstra, Tjitske, Krajewska-Walasek, Małgorzata, Kramer, Nancy, Maas, Saskia M., Maciel, Patricia, Mancini, Grazia M.S., Maystadt, Isabelle, McKee, Shane, Milunsky, Jeff M., Nampoothiri, Sheela, Newbury-Ecob, Ruth, Nikkel, Sarah M., Parker, Michael J., Pérez-Jurado, Luis A., Robertson, Stephen P., Rooryck, Caroline, Shears, Debbie, Silengo, Margherita, Singh, Ankur, Smigiel, Robert, Soares, Gabriela, Splitt, Miranda, Stewart, Helen, Sweeney, Elizabeth, Tassabehji, May, Tuysuz, Beyhan, van Eerde, Albertien M., Vincent-Delorme, Catherine, Wilson, Louise C., Yesil, Gozde

    Veröffentlicht in Human mutation

    Volltext
    Artikel
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20