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	41.	Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation. [electronic resource] by de Coo, I F Smeets, H J Gabreëls, F J Arts, N van Oost, B A Producer: 19960716 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	42.	New distal marker closely linked to the fragile X locus. [electronic resource] by Hulsebos, T J Oostra, B A Broersen, S Smits, A van Oost, B A Westerveld, A Producer: 19910912 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Biogenic amine metabolite patterns in the urine of monoamine oxidase A-deficient patients. A possible tool for diagnosis. [electronic resource] by Abeling, N G van Gennip, A H Overmars, H van Oost, B A Brunner, H G Producer: 19950130 In: Journal of inherited metabolic disease vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Linkage of X-linked nephrogenic diabetes insipidus with DXS52, a polymorphic DNA marker. [electronic resource] by Knoers, N vd Heyden, H von Oost, B A Monnens, L Willems, J Ropers, H H Producer: 19890405 In: Nephron vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples. [electronic resource] by De Coo, I F Gussinklo, T Arts, P J Van Oost, B A Smeets, H J Producer: 19970710 In: Journal of the neurological sciences vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	DNA analysis in diagnosis of von Willebrand disease in dogs. [electronic resource] by Slappendel, R J Versteeg, S A van Zon, P H Rothuizen, J van Oost, B A Producer: 19980928 In: The veterinary quarterly vol. 20 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome. [electronic resource] by Knoers, N van der Heyden, H van Oost, B A Ropers, H H Monnens, L Willems, J Producer: 19881019 In: Human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Evaluation of canine COL4A3 and COL4A4 as candidates for familial renal disease in the Norwegian elkhound. [electronic resource] by Wiersma, A C Millon, L V van Dongen, A M van Oost, B A Bannasch, D L Producer: 20061031 In: The Journal of heredity vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus. [electronic resource] by Knoers, N V van den Ouweland, A M Verdijk, M Monnens, L A van Oost, B A Producer: 19941121 In: Kidney international vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Nephrogenic diabetes insipidus: identification of the genetic defect. [electronic resource] by Knoers, N van den Ouweland, A Dreesen, J Verdijk, M Monnens, L A van Oost, B A Producer: 19940107 In: Pediatric nephrology (Berlin, Germany) vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Eye movement disorder: an early expression of the myotonic dystrophy gene? [electronic resource] by ter Bruggen, J P Tijssen, C C Brunner, H G van Oost, B A Bastiaensen, L A Producer: 19920507 In: Muscle & nerve vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus. [electronic resource] by Knoers, N van der Heyden, H van Oost, B A Monnens, L Willems, J Ropers, H H Producer: 19890612 In: Genomics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Enzymological versus DNA investigations in mitochondrial (encephalo-) myopathies. [electronic resource] by de Vries, D D Ruitenbeek, W de Wijs, I J Trijbels, J M van Oost, B A Producer: 19950817 In: Journal of inherited metabolic disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	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). [electronic resource] by van den Berg, L Kwant, L Hestand, M S van Oost, B A Leegwater, P A J Producer: 20061031 In: The Journal of heredity vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Tests for platelet changes, acute phase reactants and serum lipids in diabetes mellitus and peripheral vascular disease. [electronic resource] by van Oost, B A Veldhuyzen, B F van Houwelingen, H C Timmermans, A P Sixma, J J Producer: 19830407 In: Thrombosis and haemostasis vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	56.	A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome. [electronic resource] by de Vries, D D van Engelen, B G Gabreëls, F J Ruitenbeek, W van Oost, B A Producer: 19930930 In: Annals of neurology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Linkage analyses in families with nephrogenic diabetes insipidus. [electronic resource] by Knoers, N V van der Heyden, H van Oost, B A Monnens, L Willems, J Ropers, H H Producer: 19890908 In: Progress in clinical and biological research vol. 305 Availability: No items available. Save to lists Add to cart (remove)
	58.	Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe. [electronic resource] by van Oost, B A Smits, A P Dreesen, J C van den Ouweland, A M Oostra, B A Producer: 19920716 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Determination of the density distribution of human platelets--methodological aspects and comparison with other tests for platelet activation. [electronic resource] by van Oost, B A van Hien-Hagg, I H Veldhuyzen, B F Timmermans, A P Sixma, J J Producer: 19821029 In: Thrombosis and haemostasis vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	60.	Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutation. [electronic resource] by Hochberg, Z Van Lieburg, A Even, L Brenner, B Lanir, N Van Oost, B A Knoers, N V Producer: 19970311 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 130 results.