Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Karin Jantz"'
Autor:
Karin Jantz, Christiane Spaich, Nitin Sabherwal, Georg K. Hinkel, Ralph Röth, Hetty J. van der Kamp, Cheryll Tickle, Fiona Bangs, Gudrun A. Rappold, Johannes Kapeller, Eva Tiecke, Birgit Weiss, Berthold P. Hauffa
Publikováno v:
Human Molecular Genetics. 16:210-222
Defects in long-range regulatory elements have recently emerged as previously underestimated factors in the genesis of human congenital disorders. Léri-Weill dyschondrosteosis is a dominant skeletal malformation syndrome caused by mutations in the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3e510767a66a6dcfbb7984ba9666291
https://doi.org/10.1093/hmg/ddl470
https://doi.org/10.1093/hmg/ddl470
Autor:
Nitin Sabherwal, Ralph Röth, Katja U. Schneider, Nadja Muncke, Karin Jantz, Werner F. Blum, Gordon B. Cutler, Gudrun A. Rappold
Publikováno v:
The American Journal of Human Genetics. (1):89-96
Human growth is influenced not only by environmental and internal factors but also by a large number of different genes. One of these genes, SHOX, is believed to play a major role in growth, since defects in this homeobox-containing gene on the sex c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fb16745f1710e958b5b40442c965f59