Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Annemieke Van Der Hout"'
Autor:
Julia El Mecky, Lennart Johansson, Mirjam Plantinga, Angela Fenwick, Anneke Lucassen, Trijnie Dijkhuizen, Annemieke van der Hout, Kate Lyle, Irene van Langen
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-9 (2019)
Abstract Background In recent years, the amount of genomic data produced in clinical genetics services has increased significantly due to the advent of next-generation sequencing. This influx of genomic information leads to continuous changes in know
Externí odkaz:
https://doaj.org/article/71a25449dfcd449d8dd588732a2841a5
Autor:
Lieke Lanjouw, Marian Mourits, Joost Bart, Arja Ter Elst, Lieke Berger, Annemieke Van Der Hout, Naufil Alam, Geertruida De Bock
Publikováno v:
E-Posters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b46f05625f031d0f7a7d81e97185cfc6
https://doi.org/10.1136/ijgc-2022-igcs.360
https://doi.org/10.1136/ijgc-2022-igcs.360
Autor:
Marie-José H. van den Boogaard, Hans Kristian Ploos van Amstel, Yvon Bronkhorst, Dick Lindhout, Marco S. Cune, Eric A. M. Hennekam, Annemieke van der Hout, Marijn Créton
Publikováno v:
JOURNAL OF MEDICAL GENETICS, 49(5), 327-331. BMJ PUBLISHING GROUP
Background Dental agenesis is the most common, often heritable, developmental anomaly in humans. Mutations in MSX1, PAX9, AXIN2 and the ectodermal dysplasia genes EDA, EDAR and EDARADD have been detected in familial severe tooth agenesis. However, un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1f81edcaa40e09ec4ef4f2884f58e69
https://research.rug.nl/en/publications/e378985e-d460-4651-b2a4-cdcb6d319300
https://research.rug.nl/en/publications/e378985e-d460-4651-b2a4-cdcb6d319300