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	61.	Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation. [electronic resource] by Traupe, H Müller, D Atherton, D Kalter, D C Cremers, F P van Oost, B A Ropers, H H Producer: 19920929 In: Human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Listeria monocytogenes meningitis and decreased phagocytosis associated with iron overload. [electronic resource] by van Asbeck, B S Verbrugh, H A van Oost, B A Marx, J J Imhof, H W Verhoef, J Producer: 19820527 In: British medical journal (Clinical research ed.) vol. 284 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Cloning, characterization, and physical mapping of the canine Prop-1 gene (PROP1): exclusion as a candidate for combined pituitary hormone deficiency in German shepherd dogs. [electronic resource] by Lantinga-van Leeuwen, I S Kooistra, H S Mol, J A Renier, C Breen, M van Oost, B A Producer: 20000613 In: Cytogenetics and cell genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Isolation of DNA markers informative in purebred dog families by genomic representational difference analysis (gRDA). [electronic resource] by Everts, R E Versteeg, S A Renier, C Vignaux, F Groot, P C Rothuizen, J van Oost, B A Producer: 20000926 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Phenotyping of aggressive behavior in golden retriever dogs with a questionnaire. [electronic resource] by van den Berg, L Schilder, M B H de Vries, H Leegwater, P A J van Oost, B A Producer: 20070716 In: Behavior genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Presymptomatic diagnosis of myotonic dystrophy. [electronic resource] by Brunner, H G Nillesen, W van Oost, B A Jansen, G Wieringa, B Ropers, H H Smeets, H J Producer: 19930107 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Aquaporins: from physiology to nephrogenic diabetes insipidus. [electronic resource] by Knoers, N Van Lieburg, A F Monnens, L A Van Oost, B A Deen, P M Van Os, C Producer: 19961210 In: Advances in nephrology from the Necker Hospital vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	68.	X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder. [electronic resource] by de Vries, D D de Wijs, I J Wolff, G Ketelsen, U P Ropers, H H van Oost, B A Producer: 19930419 In: Human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male. [electronic resource] by Smits, A P van Oost, B A de Haan, A F Hamel, B C Dreesen, J C Smeets, D F 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)
	70.	A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19. [electronic resource] by Brunner, H G Smeets, H Lambermon, H M Coerwinkel-Driessen, M van Oost, B A Wieringa, B Ropers, H H Producer: 19900309 In: Genomics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications. [electronic resource] by Samson, J F Barth, P G de Vries, J I Menko, F H Ruitenbeek, W van Oost, B A Jakobs, C Producer: 19941213 In: European journal of pediatrics vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Cloning of the canine gene encoding transcription factor Pit-1 and its exclusion as candidate gene in a canine model of pituitary dwarfism. [electronic resource] by Lantinga-van Leeuwen, I S Mol, J A Kooistra, H S Rijnberk, A Breen, M Renier, C van Oost, B A Producer: 20000203 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patients. [electronic resource] by Kluijtmans, L A Blom, H J Boers, G H van Oost, B A Trijbels, F J van den Heuvel, L P Producer: 19950911 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family. [electronic resource] by Sistermans, E A de Wijs, I J de Coo, R F Smit, L M Menko, F H van Oost, B A Producer: 19960920 In: Human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28. [electronic resource] by Oostra, B A Majoor-Krakauer, D F van Hemel, J O Bakker, E Callen, D F Schmidt, M van Oost, B A Producer: 19910521 In: American journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Two intronic mutations in the adrenoleukodystrophy gene. [electronic resource] by Kemp, S Ligtenberg, M J van Geel, B M Barth, P G Sarde, C O van Oost, B A Bolhuis, P A Producer: 19960207 In: Human mutation vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish population. [electronic resource] by Sistermans, E A de Coo, R F van Beerendonk, H M Poll-The, B T Kleijer, W J van Oost, B A Producer: 20001026 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine. [electronic resource] by Deen, P M Verdijk, M A Knoers, N V Wieringa, B Monnens, L A van Os, C H van Oost, B A Producer: 19940425 In: Science (New York, N.Y.) vol. 264 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus. [electronic resource] by van den Ouweland, A M Dreesen, J C Verdijk, M Knoers, N V Monnens, L A Rocchi, M van Oost, B A Producer: 19930624 In: Nature genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	80.	[Keratosis follicularis spinulosa decalvans (Siemens I syndrome), initial results of molecular genetic research]. [electronic resource] by Oosterwijk, J C van Osch, L D Wittebol-Post, D Nelen, M van Zandvoort, P Oranje, A P van Oost, B A Producer: 19930318 In: Klinische Monatsblatter fur Augenheilkunde vol. 201 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 128 results.