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Merel C van Maarle

Showing results (1-10 of 33) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|January 8, 2011
[The joys and burdens within clinical genetics--paternal discrepancy causes dilemmas]Cora M Aalfs, Merel C van Maarle
Biochimica Et Biophysica Acta|July 17, 2012
Genetics of early miscarriageMerel M J van den Berg, Merel C van Maarle, Madelon van Wely, et al.
The British Journal of Oral & Maxillofacial Surgery|May 23, 2006
DNA analysis of the SH3BP2 gene in patients with aggressive central giant cell granulomaJan de Lange, Merel C van Maarle, Hans P van den Akker, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|February 27, 2007
A new mutation in the SH3BP2 gene showing reduced penetrance in a family affected with cherubismJan de Lange, Merel C van Maarle, Hans P van den Akker, et al.
European Journal of Human Genetics : EJHG|May 14, 2015
Do people from the Jewish community prefer ancestry-based or pan-ethnic expanded carrier screening?Kim C A Holtkamp, Merel C van Maarle, Maria J E Schouten, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 24, 2015
A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutationsEmma Beeldman, Anneke J van der Kooi, Marianne de Visser, et al.
BMJ (Clinical Research Ed.)|June 8, 2002
Follow up after a family based genetic screening programme for familial hypercholesterolaemia: is screening alone enough?Merel C Van Maarle, Marlies E A Stouthard, Perla J Marang-Van De Mheen, et al.
European Journal of Public Health|August 4, 2016
Factors for successful implementation of population-based expanded carrier screening: learning from existing initiativesKim C A Holtkamp, Inge B Mathijssen, Phillis Lakeman, et al.
Prenatal Diagnosis|September 2, 2025
The Influence of the Introduction of Fetal Anomaly Scans on Pregnancy Terminations in Cases of Upper Limb Anomalies: A Retrospective Cohort Study From 2000 to 2023Arda Arduç, Eline Huiberts, Margriet H M van Doesburg, et al.
Journal of Clinical Lipidology|January 5, 2023
Counseling couples at risk of having a child with homozygous familial hypercholesterolemia - Clinical experience and recommendationsTycho R Tromp, M Doortje Reijman, Albert Wiegman, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Nederlands Tijdschrift Voor Geneeskunde|January 8, 2011
[The joys and burdens within clinical genetics--paternal discrepancy causes dilemmas]Cora M Aalfs, Merel C van Maarle
Biochimica Et Biophysica Acta|July 17, 2012
Genetics of early miscarriageMerel M J van den Berg, Merel C van Maarle, Madelon van Wely, et al.
The British Journal of Oral & Maxillofacial Surgery|May 23, 2006
DNA analysis of the SH3BP2 gene in patients with aggressive central giant cell granulomaJan de Lange, Merel C van Maarle, Hans P van den Akker, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|February 27, 2007
A new mutation in the SH3BP2 gene showing reduced penetrance in a family affected with cherubismJan de Lange, Merel C van Maarle, Hans P van den Akker, et al.
European Journal of Human Genetics : EJHG|May 14, 2015
Do people from the Jewish community prefer ancestry-based or pan-ethnic expanded carrier screening?Kim C A Holtkamp, Merel C van Maarle, Maria J E Schouten, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 24, 2015
A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutationsEmma Beeldman, Anneke J van der Kooi, Marianne de Visser, et al.
BMJ (Clinical Research Ed.)|June 8, 2002
Follow up after a family based genetic screening programme for familial hypercholesterolaemia: is screening alone enough?Merel C Van Maarle, Marlies E A Stouthard, Perla J Marang-Van De Mheen, et al.
European Journal of Public Health|August 4, 2016
Factors for successful implementation of population-based expanded carrier screening: learning from existing initiativesKim C A Holtkamp, Inge B Mathijssen, Phillis Lakeman, et al.
Prenatal Diagnosis|September 2, 2025
The Influence of the Introduction of Fetal Anomaly Scans on Pregnancy Terminations in Cases of Upper Limb Anomalies: A Retrospective Cohort Study From 2000 to 2023Arda Arduç, Eline Huiberts, Margriet H M van Doesburg, et al.
Journal of Clinical Lipidology|January 5, 2023
Counseling couples at risk of having a child with homozygous familial hypercholesterolemia - Clinical experience and recommendationsTycho R Tromp, M Doortje Reijman, Albert Wiegman, et al.
Pageof 4