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Genetic Testing|February 3, 2005
Preconceptional cystic fibrosis carrier screening: opinions of general practitioners, gynecologists, and pediatricians in the NetherlandsMarieke J H Baars, Lidewij Henneman, Leo P ten KateGenetics in Medicine : Official Journal of the American College of Medical Genetics|November 23, 2005
Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problemMarieke J H Baars, Lidewij Henneman, Leo P Ten KateCommunity Genetics|September 28, 2006
Genetics education for non-genetic health care professionals in the Netherlands (2002)Anne Marie C Plass, Marieke J H Baars, Frits A Beemer, et al.Patient Education and Counseling|June 5, 2003
Comparison of activities and attitudes of general practitioners concerning genetic counseling over a 10-year time-spanMarieke J H Baars, Denhard J de Smit, Miranda W Langendam, et al.Trials|January 14, 2010
Losartan therapy in adults with Marfan syndrome: study protocol of the multi-center randomized controlled COMPARE trialTeodora Radonic, Piet de Witte, Marieke J H Baars, et al.American Journal of Medical Genetics. Part A|May 23, 2013
The value of the clinical geneticist caring for adults with congenital heart disease: diagnostic yield and patients' perspectiveKlaartje van Engelen, Marieke J H Baars, Joyce P Felix, et al.American Journal of Medical Genetics. Part A|June 15, 2011
Adults with congenital heart disease: patients' knowledge and concerns about inheritanceKlaartje van Engelen, Marieke J H Baars, Lotte T van Rongen, et al.European Journal of Human Genetics : EJHG|November 24, 2021
A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 25, 2013
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7Alexa M C Vermeer, Klaartje van Engelen, Alex V Postma, et al.American Journal of Medical Genetics. Part A|August 8, 2014
A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defectsRajiv A Mohan, Klaartje van Engelen, Sonia Stefanovic, et al.Pageof 3