Nijhof, Bonnie
33  results:
Search for persons X
?
5

Converging evidence does not support GIT1 as an ADHD risk g..:

Klein, Marieke ; van der Voet, Monique ; Harich, Benjamin...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  168 (2015)  6 - p. 492-507 , 2015
 
?
12

A homozygous FITM2 mutation causes a deafness-dystonia synd..:

Seco, Celia Zazo ; Castells-Nobau, Anna ; Joo, Seol-hee...
Seco , C Z , Castells-Nobau , A , Joo , S , Schraders , M , Foo , J N , van der Voet , M , Velan , S S , Nijhof , B , Oostrik , J , de Vrieze , E , Katana , R , Mansoor , A , Huynen , M , Szklarczyk , R , Oti , M , Tranebjaerg , L , van Wijk , E , Scheffer-de Gooyert , J M , Siddique , S , Baets , J , de Jonghe , P , Kazmi , S A R , Sadananthan , S A , van de Warrenburg , B P , Khor , C C , Goepfert , M C , Qamar , R , Schenck , A , Kremer , H & Siddiqi , S 2017 , ' A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy ' , Disease Models & Mechanisms , vol. 10 , no. 2 , pp. 105-118 . https://doi.org/10.1242/dmm.026476.  , 2017
 
?
15

A New Fiji-Based Algorithm That Systematically Quantifies N..:

Nijhof, Bonnie ; Castells Nobau, Anna ; Wolf, Louis...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pcbi.1004823.  , 2016
 
1-15