Results of search for 'au:"STONE, E"' › مکتبة رقمیه للعلوم الطبيه catalog

Refine your search

Availability
- Limit to records with available items
Authors
Topics
- Adolescent
- Adult
- Aged
- Animals
- Child
- Eye Proteins
- Female
- Humans
- Male
- Middle Aged
- Mutation
- Pedigree
- Rats
- United States
- drug effects
- genetics
- metabolism
- methods
- pharmacology
- physiology
- Show more
- Show less
Languages
- English
- French
- g d

	361.	A gene for familial juvenile polyposis maps to chromosome 18q21.1. [electronic resource] by Howe, J R Ringold, J C Summers, R W Mitros, F A Nishimura, D Y Stone, E M Producer: 19980521 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	362.	RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function. [electronic resource] by Kemp, C M Jacobson, S G Cideciyan, A V Kimura, A E Sheffield, V C Stone, E M Producer: 19940826 In: Investigative ophthalmology & visual science vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	363.	Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma. [electronic resource] by Johnson, A T Drack, A V Kwitek, A E Cannon, R L Stone, E M Alward, W L Producer: 19930524 In: Ophthalmology vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	364.	Procollagen II gene mutation in Stickler syndrome. [electronic resource] by Brown, D M Nichols, B E Weingeist, T A Sheffield, V C Kimura, A E Stone, E M Producer: 19921207 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	365.	Determination of the enzymes responsible for activation of the heterocyclic amine 2-amino-3-methylimidazo[4,5-f]quinoline in the human breast. [electronic resource] by Williams, J A Stone, E M Millar, B C Gusterson, B A Grover, P L Phillips, D H Producer: 19990329 In: Pharmacogenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	366.	Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification. [electronic resource] by Sheffield, V C Kraiem, Z Beck, J C Nishimura, D Stone, E M Salameh, M Sadeh, O Glaser, B Producer: 19960703 In: Nature genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	367.	Evidence that carotid bodies play an important role in glucoregulation in vivo. [electronic resource] by Koyama, Y Coker, R H Stone, E E Lacy, D B Jabbour, K Williams, P E Wasserman, D H Producer: 20000925 In: Diabetes vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	368.	A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree. [electronic resource] by Schnieders, M J Goar, W Griess, M Roos, B R Scheetz, T E Stone, E M Fingert, J H Producer: 20181211 In: Eye (London, England) vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	369.	Night blindness in Sorsby's fundus dystrophy reversed by vitamin A. [electronic resource] by Jacobson, S G Cideciyan, A V Regunath, G Rodriguez, F J Vandenburgh, K Sheffield, V C Stone, E M Producer: 19951120 In: Nature genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	370.	A nonsense mutation in the retinal specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred kindred from Jordan. [electronic resource] by El-Shanti, H Al-Salem, M El-Najjar, M Ajlouni, K Beck, J Sheffiled, V C Stone, E M Producer: 20000113 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	371.	Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes. [electronic resource] by Sunden, S L Alward, W L Nichols, B E Rokhlina, T R Nystuen, A Stone, E M Sheffield, V C Producer: 19970513 In: Genome research vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	372.	A community education monitoring system: methods from the Stanford Five-City Project, the Minnesota Heart Health Program and the Pawtucket Heart Health Program. [electronic resource] by Flora, J A Lefebvre, R C Murray, D M Stone, E J Assaf, A Mittelmark, M B Finnegan, J R Producer: 20001010 In: Health education research vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	373.	Need for coronary artery bypass grafting in Newfoundland and Labrador: the impact of increased demand. [electronic resource] by Kent, G M Power, L Gregory, D M Barrett, B J MacCallum, G C Stone, E W Parfrey, P S Producer: 20040603 In: The Canadian journal of cardiology vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	374.	CATCH: process evaluation of environmental factors and programs. [electronic resource] by Elder, J P McGraw, S A Stone, E J Reed, D B Harsha, D W Greene, T Wambsgans, K C Producer: 19940331 In: Health education quarterly vol. Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	375.	Sub-retinal pigment epithelial deposits in a dominant late-onset retinal degeneration. [electronic resource] by Kuntz, C A Jacobson, S G Cideciyan, A V Li, Z Y Stone, E M Possin, D Milam, A H Producer: 19960918 In: Investigative ophthalmology & visual science vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	376.	Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosa. [electronic resource] by Millá, E Héon, E Grounauer, P A Piguet, B Ducrey, N Stone, E M Schorderet, D F Munier, F L Producer: 19990210 In: Ophthalmic genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	377.	Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration. [electronic resource] by Stone, E M Webster, A R Vandenburgh, K Streb, L M Hockey, R R Lotery, A J Sheffield, V C Producer: 19981221 In: Nature genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	378.	Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomaly. [electronic resource] by Mellott, M L Brown, J Fingert, J H Taylor, C M Keech, R V Sheffield, V C Stone, E M Producer: 19991221 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	379.	Patterns of physical activity among American Indian children: an assessment of barriers and support. [electronic resource] by Thompson, J L Davis, S M Gittelsohn, J Going, S Becenti, A Metcalfe, L Stone, E Harnack, L Ring, K Producer: 20020314 In: Journal of community health vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	380.	Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. [electronic resource] by Alward, W L Semina, E V Kalenak, J W Héon, E Sheth, B P Stone, E M Murray, J C Producer: 19980129 In: American journal of ophthalmology vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 512 results.