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F Baas

Showing results (41-50 of 245) with videos related to

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American Journal of Human Genetics|March 1, 1991
Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28P A Bolhuis, G W Hensels, T J Hulsebos, et al.
Journal of Clinical Medicine|March 3, 2021
Diagnosis and Risk Prediction of Dilated Cardiomyopathy in the Era of Big Data and GenomicsArjan Sammani, Annette F Baas, Folkert W Asselbergs, et al.
Neurology|October 25, 2006
Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 geneF Meggouh, H M E Bienfait, M A J Weterman, et al.
Biochimica Et Biophysica Acta|September 8, 1993
Molecular basis of an adult form of Sandhoff disease: substitution of glutamine for arginine at position 505 of the beta-chain of beta-hexosaminidase results in a labile enzymeP A Bolhuis, N J Ponne, H Bikker, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 15, 1985
[DNA analysis and genetic counseling]P A Bolhuis, F Baas, G J van Ommen, et al.
Endocrinology|January 1, 1997
Effects of maternal thyroid status on thyroid hormones and growth in congenitally hypothyroid goat fetuses during the second half of gestationP A Piosik, M van Groenigen, J van Doorn, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.
Human Molecular Genetics|December 23, 1999
Alzheimer's presenilin 1 is a putative membrane receptor for rab GDP dissociation inhibitorW Scheper, R Zwart, P van der Sluijs, et al.
European Journal of Preventive Cardiology|December 13, 2019
Mitral valve prolapse, a familial condition worth screening for?Jakub J Regieli, Maarten J Cramer, Annette F Baas, et al.
Nucleic Acids Research|July 11, 1986
The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kbF Baas, G J van Ommen, H Bikker, et al.
Pageof 25

Showing results (41-50 of 245) with videos related to

Sort By:
Pageof 25
American Journal of Human Genetics|March 1, 1991
Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28P A Bolhuis, G W Hensels, T J Hulsebos, et al.
Journal of Clinical Medicine|March 3, 2021
Diagnosis and Risk Prediction of Dilated Cardiomyopathy in the Era of Big Data and GenomicsArjan Sammani, Annette F Baas, Folkert W Asselbergs, et al.
Neurology|October 25, 2006
Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 geneF Meggouh, H M E Bienfait, M A J Weterman, et al.
Biochimica Et Biophysica Acta|September 8, 1993
Molecular basis of an adult form of Sandhoff disease: substitution of glutamine for arginine at position 505 of the beta-chain of beta-hexosaminidase results in a labile enzymeP A Bolhuis, N J Ponne, H Bikker, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 15, 1985
[DNA analysis and genetic counseling]P A Bolhuis, F Baas, G J van Ommen, et al.
Endocrinology|January 1, 1997
Effects of maternal thyroid status on thyroid hormones and growth in congenitally hypothyroid goat fetuses during the second half of gestationP A Piosik, M van Groenigen, J van Doorn, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.
Human Molecular Genetics|December 23, 1999
Alzheimer's presenilin 1 is a putative membrane receptor for rab GDP dissociation inhibitorW Scheper, R Zwart, P van der Sluijs, et al.
European Journal of Preventive Cardiology|December 13, 2019
Mitral valve prolapse, a familial condition worth screening for?Jakub J Regieli, Maarten J Cramer, Annette F Baas, et al.
Nucleic Acids Research|July 11, 1986
The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kbF Baas, G J van Ommen, H Bikker, et al.
Pageof 25