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B A van Oost

Showing results (31-40 of 107) with videos related to

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Human Genetics|July 1, 1991
New distal marker closely linked to the fragile X locusT J Hulsebos, B A Oostra, S Broersen, et al.
Journal of the Neurological Sciences|July 1, 1997
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samplesI F De Coo, T Gussinklo, P J Arts, et al.
Thrombosis and Haemostasis|December 27, 1982
Tests for platelet changes, acute phase reactants and serum lipids in diabetes mellitus and peripheral vascular diseaseB A van Oost, B F Veldhuyzen, H C van Houwelingen, et al.
Kidney International|July 1, 1994
Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidusN V Knoers, A M van den Ouweland, M Verdijk, et al.
The Journal of Heredity|October 28, 2005
Structure and variation of three canine genes involved in serotonin binding and transport: the serotonin receptor 1A gene (htr1A), serotonin receptor 2A gene (htr2A), and serotonin transporter gene (slc6A4)L van den Berg, L Kwant, M S Hestand, et al.
Muscle & Nerve|March 1, 1992
Eye movement disorder: an early expression of the myotonic dystrophy gene?J P ter Bruggen, C C Tijssen, H G Brunner, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1993
Nephrogenic diabetes insipidus: identification of the genetic defectN Knoers, A van den Ouweland, J Dreesen, et al.
Annals of Neurology|September 1, 1993
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndromeD D de Vries, B G van Engelen, F J Gabreëls, et al.
The Journal of Heredity|July 15, 2005
Evaluation of canine COL4A3 and COL4A4 as candidates for familial renal disease in the Norwegian elkhoundA C Wiersma, L V Millon, A M van Dongen, et al.
Human Genetics|September 1, 1988
Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosomeN Knoers, H van der Heyden, B A van Oost, et al.
Pageof 11

Showing results (31-40 of 107) with videos related to

Sort By:
Pageof 11
Human Genetics|July 1, 1991
New distal marker closely linked to the fragile X locusT J Hulsebos, B A Oostra, S Broersen, et al.
Journal of the Neurological Sciences|July 1, 1997
A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samplesI F De Coo, T Gussinklo, P J Arts, et al.
Thrombosis and Haemostasis|December 27, 1982
Tests for platelet changes, acute phase reactants and serum lipids in diabetes mellitus and peripheral vascular diseaseB A van Oost, B F Veldhuyzen, H C van Houwelingen, et al.
Kidney International|July 1, 1994
Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidusN V Knoers, A M van den Ouweland, M Verdijk, et al.
The Journal of Heredity|October 28, 2005
Structure and variation of three canine genes involved in serotonin binding and transport: the serotonin receptor 1A gene (htr1A), serotonin receptor 2A gene (htr2A), and serotonin transporter gene (slc6A4)L van den Berg, L Kwant, M S Hestand, et al.
Muscle & Nerve|March 1, 1992
Eye movement disorder: an early expression of the myotonic dystrophy gene?J P ter Bruggen, C C Tijssen, H G Brunner, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1993
Nephrogenic diabetes insipidus: identification of the genetic defectN Knoers, A van den Ouweland, J Dreesen, et al.
Annals of Neurology|September 1, 1993
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndromeD D de Vries, B G van Engelen, F J Gabreëls, et al.
The Journal of Heredity|July 15, 2005
Evaluation of canine COL4A3 and COL4A4 as candidates for familial renal disease in the Norwegian elkhoundA C Wiersma, L V Millon, A M van Dongen, et al.
Human Genetics|September 1, 1988
Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosomeN Knoers, H van der Heyden, B A van Oost, et al.
Pageof 11