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H Bikker

Showing results (11-20 of 29) with videos related to

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Human Genetics|April 1, 1989
Eco RI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2H Bikker, P A Bolhuis, G Vassart, et al.
Nucleic Acids Research|August 25, 1988
XmnI RFLP at 5q13 detected by a 0.49 kb Xmn I fragment of human hexosaminidase (HEXB) cDNAH Bikker, M F Meyer, A C Merk, 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.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Serum thyroglobulin levels: the physiological decrease in infancy and the absence in athyroidismJ L Ket, J J De Vijder, H Bikker, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1994
A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidismH Bikker, M T den Hartog, F Baas, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update)B Bakker, H Bikker, T Vulsma, 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 mutationS Alsters, L Wong, L Peferoen, et al.
European Journal of Biochemistry|July 11, 1998
The gene for the human Src-like adaptor protein (hSLAP) is located within the 64-kb intron of the thyroglobulin geneP H Meijerink, P Yanakiev, I Zorn, et al.
The Netherlands Journal of Medicine|May 31, 2018
Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levelsK F de Geus, A A Anas, R Franssen, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Regional localization of the gene for thyroid peroxidase to human chromosome 2pter----p12J J de Vijlder, C Dinsart, F Libert, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Human Genetics|April 1, 1989
Eco RI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2H Bikker, P A Bolhuis, G Vassart, et al.
Nucleic Acids Research|August 25, 1988
XmnI RFLP at 5q13 detected by a 0.49 kb Xmn I fragment of human hexosaminidase (HEXB) cDNAH Bikker, M F Meyer, A C Merk, 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.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Serum thyroglobulin levels: the physiological decrease in infancy and the absence in athyroidismJ L Ket, J J De Vijder, H Bikker, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1994
A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidismH Bikker, M T den Hartog, F Baas, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update)B Bakker, H Bikker, T Vulsma, 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 mutationS Alsters, L Wong, L Peferoen, et al.
European Journal of Biochemistry|July 11, 1998
The gene for the human Src-like adaptor protein (hSLAP) is located within the 64-kb intron of the thyroglobulin geneP H Meijerink, P Yanakiev, I Zorn, et al.
The Netherlands Journal of Medicine|May 31, 2018
Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levelsK F de Geus, A A Anas, R Franssen, et al.
Cytogenetics and Cell Genetics|January 1, 1988
Regional localization of the gene for thyroid peroxidase to human chromosome 2pter----p12J J de Vijlder, C Dinsart, F Libert, et al.
Pageof 3