Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Markus Homberg"'
Autor:
Romy van de Putte, Charlotte H W Wijers, Heiko Reutter, Sita H Vermeulen, Carlo L M Marcelis, Erwin Brosens, Paul M A Broens, Markus Homberg, Michael Ludwig, Ekkehart Jenetzky, Nadine Zwink, Cornelius E J Sloots, Annelies de Klein, Alice S Brooks, Robert M W Hofstra, Sophie A C Holsink, Loes F M van der Zanden, Tessel E Galesloot, Paul Kwong-Hang Tam, Marloes Steehouwer, Rocio Acuna-Hidalgo, Maartje van de Vorst, Lambertus A Kiemeney, Maria-Mercè Garcia-Barceló, Ivo de Blaauw, Han G Brunner, Nel Roeleveld, Iris A L M van Rooij
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0217477 (2019)
IntroductionAnorectal malformations (ARM) are rare congenital malformations, resulting from disturbed hindgut development. A genetic etiology has been suggested, but evidence for the involvement of specific genes is scarce. We evaluated the contribut
Externí odkaz:
https://doaj.org/article/641fb7e6ff264466bd436fd610bb6de0
Autor:
Erwin Brosens, Heiko Reutter, Han G. Brunner, Sophie A. C. Holsink, Charlotte H. W. Wijers, Ekkehart Jenetzky, Romy van de Putte, Maria-Mercè Garcia-Barceló, Nel Roeleveld, Marloes Steehouwer, Paul M. A. Broens, Robert M.W. Hofstra, Paul K.H. Tam, Carlo Marcelis, Lambertus A. Kiemeney, Nadine Zwink, Sita H. Vermeulen, Maartje van de Vorst, Alice S. Brooks, Annelies de Klein, Tessel E. Galesloot, Cornelius E. J. Sloots, Michael Ludwig, Ivo de Blaauw, Loes F.M. van der Zanden, Markus Homberg, Iris A.L.M. van Rooij, Rocio Acuna-Hidalgo
Publikováno v:
PLOS ONE, 14(5):0217477. Public Library of Science
PLoS One (online), 14(5):e0217477. Public Library of Science
PLoS ONE, 14(5):0217477. PUBLIC LIBRARY SCIENCE
PLoS ONE, Vol 14, Iss 5, p e0217477 (2019)
PLoS ONE
PLoS One, 14, 5
PLoS One, 14
PLoS One (online), 14(5):e0217477. Public Library of Science
PLoS ONE, 14(5):0217477. PUBLIC LIBRARY SCIENCE
PLoS ONE, Vol 14, Iss 5, p e0217477 (2019)
PLoS ONE
PLoS One, 14, 5
PLoS One, 14
IntroductionAnorectal malformations (ARM) are rare congenital malformations, resulting from disturbed hindgut development. A genetic etiology has been suggested, but evidence for the involvement of specific genes is scarce. We evaluated the contribut