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Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
November 29, 2018
Myotonic dystrophy presenting as severely dilated cardiomyopathy with out-of-hospital cardiac arrest
M Isrie, L Wong, J M van Hagen, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
August 30, 2019
Non-sustained ventricular tachycardias, conduction disorders and an impaired left ventricular ejection fraction in a 32-year-old woman
S Alsters, Y Polyukhovych, H Bikker, et al.
Mechanisms of Development
|
May 4, 2001
Expression of Irx6 during mouse morphogenesis
J Mummenhoff, A C Houweling, T Peters, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
December 19, 2000
Sensitive nonradioactive detection of mRNA in tissue sections: novel application of the whole-mount in situ hybridization protocol
A F Moorman, A C Houweling, P A de Boer, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
June 14, 2019
Hereditary thoracic aortic disease associated with cysteine substitution c.937T > G p.(Cys313Gly) in FBN1
E Overwater, K Van Rossum, M J H Baars, et al.
Developmental Biology
|
August 6, 2000
Patterning the embryonic heart: identification of five mouse Iroquois homeobox genes in the developing heart
V M Christoffels, A G Keijser, A C Houweling, et al.
Mechanisms of Development
|
August 25, 2001
Gene and cluster-specific expression of the Iroquois family members during mouse development
A C Houweling, R Dildrop, T Peters, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 12, 2019
Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation
S Alsters, L Wong, L Peferoen, et al.
European Journal of Pediatrics
|
April 12, 2014
The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation
E Overwater, Y Smulders, M van der Burg, et al.
Prenatal Diagnosis
|
January 30, 2010
Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes
A C Houweling, Y M de Mooij, I van der Burgt, et al.
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of 3
Search research articles
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Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
November 29, 2018
Myotonic dystrophy presenting as severely dilated cardiomyopathy with out-of-hospital cardiac arrest
M Isrie, L Wong, J M van Hagen, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
August 30, 2019
Non-sustained ventricular tachycardias, conduction disorders and an impaired left ventricular ejection fraction in a 32-year-old woman
S Alsters, Y Polyukhovych, H Bikker, et al.
Mechanisms of Development
|
May 4, 2001
Expression of Irx6 during mouse morphogenesis
J Mummenhoff, A C Houweling, T Peters, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
December 19, 2000
Sensitive nonradioactive detection of mRNA in tissue sections: novel application of the whole-mount in situ hybridization protocol
A F Moorman, A C Houweling, P A de Boer, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
June 14, 2019
Hereditary thoracic aortic disease associated with cysteine substitution c.937T > G p.(Cys313Gly) in FBN1
E Overwater, K Van Rossum, M J H Baars, et al.
Developmental Biology
|
August 6, 2000
Patterning the embryonic heart: identification of five mouse Iroquois homeobox genes in the developing heart
V M Christoffels, A G Keijser, A C Houweling, et al.
Mechanisms of Development
|
August 25, 2001
Gene and cluster-specific expression of the Iroquois family members during mouse development
A C Houweling, R Dildrop, T Peters, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 12, 2019
Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation
S Alsters, L Wong, L Peferoen, et al.
European Journal of Pediatrics
|
April 12, 2014
The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation
E Overwater, Y Smulders, M van der Burg, et al.
Prenatal Diagnosis
|
January 30, 2010
Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes
A C Houweling, Y M de Mooij, I van der Burgt, et al.
Page
of 3