Regional differences in recombination hotspots between two chicken populations

por Elferink, Martin G, van As, Pieter, Veenendaal, Tineke, Crooijmans, Richard PMA, Groenen, Martien AM
Publicado 2010

Partial duplication of the PRLR and SPEF2 genes at the late feathering locus in chicken

por Elferink, Martin G, Vallée, Amélie AA, Jungerius, Annemieke P, Crooijmans, Richard PMA, Groenen, Martien AM
Publicado 2008

Signatures of Selection in the Genomes of Commercial and Non-Commercial Chicken Breeds

por Elferink, Martin G., Megens, Hendrik-Jan, Vereijken, Addie, Hu, Xiaoxiang, Crooijmans, Richard P. M. A., Groenen, Martien A. M.
Publicado 2012

Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy‐14 cotwin

por Hochstenbach, Ron, Elferink, Martin G., van Zon, Patrick H. A., Lichtenbelt, Klaske D., van Harssel, Jeske, Schuring‐Blom, Heleen, Page‐Christiaens, Godelieve C.M.L.
Publicado 2018

Cell-free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case

por Hochstenbach, Ron, Nikkels, Peter G J, Elferink, Martin G, Oudijk, Martijn A, van Oppen, Carla, van Zon, Patrick, van Harssel, Jeske, Schuring-Blom, Heleen, Page-Christiaens, Godelieve C M L
Publicado 2015

Whole genome SNP discovery and analysis of genetic diversity in Turkey (Meleagris gallopavo)

por Aslam, Muhammad L, Bastiaansen, John WM, Elferink, Martin G, Megens, Hendrik-Jan, Crooijmans, Richard PMA, Blomberg, Le Ann, Fleischer, Robert C, Van Tassell, Curtis P, Sonstegard, Tad S, Schroeder, Steven G, Groenen, Martien AM, Long, Julie A
Publicado 2012

Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndrome

por Ramirez-Martinez, Andres, Zhang, Yichi, van den Boogaard, Marie-Jose, McAnally, John R., Rodriguez-Caycedo, Cristina, Chai, Andreas C., Chemello, Francesco, Massink, Maarten P.G., Cuppen, Inge, Elferink, Martin G., van Es, Robert J.J., Janssen, Nard G., Walraven-van Oijen, Linda P.A.M., Liu, Ning, Bassel-Duby, Rhonda, van Jaarsveld, Richard H., Olson, Eric N.
Publicado 2022

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study

por Van Opstal, Diane, van Maarle, Merel C, Lichtenbelt, Klaske, Weiss, Marjan M, Schuring-Blom, Heleen, Bhola, Shama L, Hoffer, Mariette J V, Huijsdens-van Amsterdam, Karin, Macville, Merryn V, Kooper, Angelique J A, Faas, Brigitte H W, Govaerts, Lutgarde, Tan-Sindhunata, Gita M, den Hollander, Nicolette, Feenstra, Ilse, Galjaard, Robert-Jan H, Oepkes, Dick, Ghesquiere, Stijn, Brouwer, Rutger W W, Beulen, Lean, Bollen, Sander, Elferink, Martin G, Straver, Roy, Henneman, Lidewij, Page-Christiaens, Godelieve C, Sistermans, Erik A
Publicado 2018