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	81.	Construction and utility of a human chromosome 22-specific Fosmid library. [electronic resource] by Kim, U J Shizuya, H Sainz, J Garnes, J Pulst, S M de Jong, P Simon, M I Producer: 19960312 In: Genetic analysis : biomolecular engineering vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Neurofibromatosis 2 tumour suppressor schwannomin interacts with betaII-spectrin. [electronic resource] by Scoles, D R Huynh, D P Morcos, P A Coulsell, E R Robinson, N G Tamanoi, F Pulst, S M Producer: 19980423 In: Nature genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1. [electronic resource] by Costa, R M Yang, T Huynh, D P Pulst, S M Viskochil, D H Silva, A J Brannan, C I Producer: 20010426 In: Nature genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia. [electronic resource] by Figueroa, K P Chan, P Schöls, L Tanner, C Riess, O Perlman, S L Geschwind, D H Pulst, S M Producer: 20011101 In: Archives of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores. [electronic resource] by Nechiporuk, A Fain, P Kort, E Nee, L E Frommelt, E Polinsky, R J Korenberg, J R Pulst, S M Producer: 19930923 In: American journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion. [electronic resource] by Korenberg, J R Kalousek, D K Anneren, G Pulst, S M Hall, J G Epstein, C J Cox, D R Producer: 19910813 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Spinal tumors in patients with neurofibromatosis type 2: MR imaging study of frequency, multiplicity, and variety. [electronic resource] by Mautner, V F Tatagiba, M Lindenau, M Fünsterer, C Pulst, S M Baser, M E Kluwe, L Zanella, F E Producer: 19951019 In: AJR. American journal of roentgenology vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Screening for mutations in synaptotagmin XI in Parkinson's disease. [electronic resource] by Glass, A S Huynh, D P Franck, Th Woitalla, D Müller, Th Pulst, S M Berg, D Krüger, R Riess, O Producer: 20041005 In: Journal of neural transmission. Supplementum no. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations. [electronic resource] by Baser, M E Mautner, V F Ragge, N K Nechiporuk, A Riccardi, V M Klein, J Sainz, J Pulst, S M Producer: 19961218 In: Neurology vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	The neuroimaging and clinical spectrum of neurofibromatosis 2. [electronic resource] by Mautner, V F Lindenau, M Baser, M E Hazim, W Tatagiba, M Haase, W Samii, M Wais, R Pulst, S M Producer: 19961031 In: Neurosurgery vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	A high-resolution PAC and BAC map of the SCA2 region. [electronic resource] by Nechiporuk, T Nechiporuk, A Sahba, S Figueroa, K Shibata, H Chen, X N Korenberg, J R de Jong, P Pulst, S M Producer: 19971103 In: Genomics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2). [electronic resource] by Hayes, S Turecki, G Brisebois, K Lopes-Cendes, I Gaspar, C Riess, O Ranum, L P Pulst, S M Rouleau, G A Producer: 20001027 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12. [electronic resource] by Nechiporuk, A Lopes-Cendes, I Nechiporuk, T Starkman, S Andermann, E Rouleau, G A Weissenbach, J S Kort, E Pulst, S M Producer: 19960725 In: Neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? [electronic resource] by Waters, M F Fee, D Figueroa, K P Nolte, D Müller, U Advincula, J Coon, H Evidente, V G Pulst, S M Producer: 20060309 In: Neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map. [electronic resource] by Nechiporuk, T Nechiporuk, A Guan, X Frederick, R Figueroa, K Chumakov, I Korenberg, J R de Jong, P J Pulst, S M Producer: 19961203 In: Human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. [electronic resource] by Korenberg, J R Kawashima, H Pulst, S M Ikeuchi, T Ogasawara, N Yamamoto, K Schonberg, S A West, R Allen, L Magenis, E Producer: 19900904 In: American journal of human genetics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	97.	Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region. [electronic resource] by Kamino, K Orr, H T Payami, H Wijsman, E M Alonso, M E Pulst, S M Anderson, L O'dahl, S Nemens, E White, J A Producer: 19921112 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	98.	Stable ring chromosome 21: molecular and clinical definition of the lesion. [electronic resource] by Falik-Borenstein, T C Pribyl, T M Pulst, S M Van Dyke, D L Weiss, L Chu, M L Kraus, J Marshak, D Korenberg, J R Producer: 19930927 In: American journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. [electronic resource] by Schöls, L Gispert, S Vorgerd, M Menezes Vieira-Saecker, A M Blanke, P Auburger, G Amoiridis, G Meves, S Epplen, J T Przuntek, H Pulst, S M Riess, O Producer: 19971023 In: Archives of neurology vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission. [electronic resource] by Gouw, L G Castañeda, M A McKenna, C K Digre, K B Pulst, S M Perlman, S Lee, M S Gomez, C Fischbeck, K Gagnon, D Storey, E Bird, T Jeri, F R Ptácek, L J Producer: 19980416 In: Human molecular genetics vol. 7 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 106 results.