Treffer 1 - 17 von 17 für Suche 'Mullaney, Alex', Suchdauer: 0,93s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6

    Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections von Mis, Emily K., Brodsky, Nina N., Ionita, Cristian, Darbinyan, Armine, Drummond-Borg, Margaret, McGee, Elisabeth, Nugent, Kimberly, Ortega, Lucy, Goodkin, Howard P., Sapp, Katie, McKee, Shane, Rea, Gillian, Cooper, Nicola, O’Driscoll, Mary, Scurr, Ingrid, Abbs, Steve, Armstrong, Ruth, Raymond, Lucy, Green, Andrew, Cleary, Elaine, Lampe, Anne, Castle, Bruce, Loughlin, Sam, Izatt, Louise, Roworth, Wendy, Yau, Shu, Jewell, Rosalyn, Sarkar, Ajoy, Canham, Natalie, Burkitt-Wright, Emma, Jones, Elizabeth, Smith, Audrey, Wright, Ronnie, Henderson, Alex, Allen, Zoe, Bernhard, Birgitta, Busby, Louise, Clowes, Virginia, Blair, Edward, Stewart, Alison, Kamath, Arveen, Halai, D., Holman, J.E., Jackson, R., Lopez, F.J., Rogers, T., Savage, K., Sieghart, A., Thomas, E.R.A., Thompson, S.R., Tucci, A., Alejandro, Mercedes E., Amendola, Laura, Andrews, Ashley, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bamshad, Michael, Bayrak-Toydemir, Pinar, Botto, Lorenzo, Coakley, Terra R., Coggins, Matthew, Cooper, Cynthia M., Cunningham, Michael, Dai, Hongzheng, Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Hahn, Sihoun, Hanchard, Neil A., Hayes, Nichole, High, Frances, Hisama, Fuki M., Holm, Ingrid A., Jamal, Fariha, Kennedy, Jennifer, LeBlanc, Kimberly, Macnamara, Ellen F., Maduro, Valerie V., Mak, Bryan, McCauley, Jacob, McGee, Elisabeth, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Pace, Laura, Potocki, Lorraine, Quinlan, Aaron, Raja, Archana N., Robertson, Amy K., Rodan, Lance H., Saporta, Mario, Schaechter, Judy, Signer, Rebecca, Solem, Emily, Solnica-Krezel, Lilianna, Sutton, Shirley, Velinder, Matt, Wheeler, Matthew T., Khokha, Mustafa K.

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15

    The contribution of X-linked coding variation to severe developmental disorders von Gardner, Eugene J, Sifrim, Alejandro, Neville, Matthew D. C, Gallone, Giuseppe, FitzPatrick, David R, Firth, Helen V, Borras, Silvia, Clark, Caroline, Miedzybrodzka, Zosia, Donnelly, Deirdre, Magee, Alex, McKee, Shane, Morrison, Patrick J, Stewart, Fiona, Cooper, Nicola, Islam, Lily, Jarvis, Joanna, Lim, Derek, Morton, Jenny, Ong, Kai-Ren, Turton, Sarah, Vogt, Julie, Hills, Alison, Low, Karen, Newbury-Ecob, Ruth, Scurr, Ingrid, Tooley, Madeleine, Armstrong, Ruth, Holden, Simon, Reid, Evan, Woods, Geoff, Bradley, Lisa, Comerford, Joanne, Mavrak, Eleni, Cleary, Elaine, Baple, Emma, Brewer, Carole, Kivuva, Emma, Turnpenny, Peter, Bradley, Therese, Davidson, Rosemarie, Whiteford, Margo, Barnicoat, Angela, Hurst, Jane, Jenkins, Lucy, Jones, Wendy, Kumar, V.K.Ajith, Lees, Melissa, Male, Alison, Rosser, Elisabeth, Josifova, Dragana, Roworth, Wendy, Ryten, Mina, Yau, Shu, Campbell, Jennifer, Coates, Andrea, Dobbie, Angus, Jewell, Rosalyn, Dixit, Abhijit, Harrison, Rachel, Sharif, Abid, Suri, Mohnish, Vasudevan, Pradeep, Canham, Natalie, Howard, Emma, Weber, Astrid, Clayton-Smith, Jill, Douzgou, Sofia, Kerr, Bronwyn, Wright, Ronnie, Bourn, David, Hellens, Steve, Montgomery, Tara, Straub, Volker, Allen, Zoe, Bernhard, Birgitta, Brady, Angela, Brooks, Claire, Holder, Susan, Carmichael, Jenny, Kini, Usha, Nemeth, Andrea, Wilkie, Andrew, Albaba, Shadi, Baker, Duncan, Balasubramanian, Meena, Johnson, Diana, Stewart, Alison, Crosby, Charlene, Jin, Huilin, Lahiri, Nayana, Kamath, Arveen, Mugalaasi, Hood, Pottinger, Caroline, Procter, Annie, Varghese, Vinod, Daniels, Stacey, Hunt, David, Lachlan, Katherine, Wellesley, Diana

    Volltext bestellen
    Artikel
  16. 16
  17. 17