Defining the genetic contribution of type 2 diabetes mellitus
J van Tilburg, TW Van Haeften, P Pearson… - Journal of medical …, 2001 - jmg.bmj.com
Type 2 diabetes mellitus is a common multifactorial genetic syndrome, which is determined
by several different genes and environmental factors. It now affects 150 million people world …
by several different genes and environmental factors. It now affects 150 million people world …
[PDF][PDF] Neurology symposium report
K Taylor - JOURNAL-ROYAL COLLEGE OF PHYSICIANS OF …, 2007 - rcpe.ac.uk
ABSTRACTThe Royal College of Physicians of Edinburgh held its latest Neurology Symposium
on 9 November 2006. The topics, summarised in this report, included useful clinical …
on 9 November 2006. The topics, summarised in this report, included useful clinical …
Expanding the mutation spectrum in FSHD and ICF syndrome
TL van den Boogaard - 2018 - scholarlypublications …
In this thesis two diseases that share a common feature of hypomethylation of repetitive
DNA are studied: facioscapulohumeral muscular dystrophy (FSHD) and immunodeficiency, …
DNA are studied: facioscapulohumeral muscular dystrophy (FSHD) and immunodeficiency, …
[CITAAT][C] Facioscapulohumeral muscular dystrophy: from genetic mapping towards gene cloning
TN Wijmenga - 1993
[CITAAT][C] Ziekte en gezondheid: verborgen verschillen: genomics slaat een brug tussen disciplines
TN Wijmenga - 2004 - Universiteit Utrecht
[CITAAT][C] Wat is de waarde van ons DNA?
MH Hofker, TN Wijmenga - 2008 - Universitair Medisch Centrum …