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	101.	Chronic course of anxiety disorders in children and adolescents. [electronic resource] by Keller, M B Lavori, P W Wunder, J Beardslee, W R Schwartz, C E Roth, J Producer: 19920908 In: Journal of the American Academy of Child and Adolescent Psychiatry vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q. [electronic resource] by Wang, Y Treat, K Schroer, R J O'Brien, J E Stevenson, R E Schwartz, C E Producer: 19941018 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Clinical and behavioral characteristics in FG syndrome. [electronic resource] by Graham, J M Superneau, D Rogers, R C Corning, K Schwartz, C E Dykens, E M Producer: 19990830 In: American journal of medical genetics vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	104.	FG syndrome: report of three new families with linkage to Xq12-q22.1. [electronic resource] by Graham, J M Tackels, D Dibbern, K Superneau, D Rogers, C Corning, K Schwartz, C E Producer: 19990107 In: American journal of medical genetics vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	105.	Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene. [electronic resource] by Lebel, R R May, M Pouls, S Lubs, H A Stevenson, R E Schwartz, C E Producer: 20020819 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	DNA fingerprinting: the utilization of minisatellite probes to detect a somatic mutation in the proteus syndrome. [electronic resource] by Schwartz, C E Brown, A M Der Kaloustian, V M McGill, J J Saul, R A Producer: 19910919 In: EXS vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome. [electronic resource] by Schwartz, C E Gillessen-Kaesbach, G May, M Cappa, M Gorski, J Steindl, K Neri, G Producer: 20001207 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)
	108.	Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21. [electronic resource] by Häne, B Schroer, R J Arena, J F Lubs, H A Schwartz, C E Stevenson, R E Producer: 19970326 In: Clinical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Expanding the phenotypic spectrum of L1CAM-associated disease. [electronic resource] by Basel-Vanagaite, L Straussberg, R Friez, M J Inbar, D Korenreich, L Shohat, M Schwartz, C E Producer: 20060630 In: Clinical genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Short-term memory deficits in carrier females with KDM5C mutations. [electronic resource] by Simensen, R J Rogers, R C Collins, J S Abidi, F Schwartz, C E Stevenson, R E Producer: 20120719 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	111.	Glomerular basement membrane: evidence for collagenous domain of the alpha 3 and alpha 4 chains of collagen IV. [electronic resource] by Fagg, W R Timoneda, J Schwartz, C E Langeveld, J P Noelken, M E Hudson, B G Producer: 19900821 In: Biochemical and biophysical research communications vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Stress and course of disease in multiple sclerosis. [electronic resource] by Schwartz, C E Foley, F W Rao, S M Bernardin, L J Lee, H Genderson, M W Producer: 20000218 In: Behavioral medicine (Washington, D.C.) vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Gene for apparently nonsyndromic X-linked mental retardation (MRX32) maps to an 18-Mb region of Xp21.2-p22. [electronic resource] by Häne, B Stevenson, R E Arena, J F Lubs, H A Simensen, R J Schwartz, C E Producer: 20000517 In: American journal of medical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 gene. [electronic resource] by Lubs, H Abidi, F E Echeverri, R Holloway, L Meindl, A Stevenson, R E Schwartz, C E Producer: 20060630 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	A phenotype of early infancy predicts reactivity of the amygdala in male adults. [electronic resource] by Schwartz, C E Kunwar, P S Greve, D N Kagan, J Snidman, N C Bloch, R B Producer: 20130227 In: Molecular psychiatry vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Inhibition of urokinase by 4-substituted benzo[b]thiophene-2-carboxamidines: an important new class of selective synthetic urokinase inhibitor. [electronic resource] by Towle, M J Lee, A Maduakor, E C Schwartz, C E Bridges, A J Littlefield, B A Producer: 19930621 In: Cancer research vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	117.	Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1. [electronic resource] by Marinoni, J C Stevenson, R E Evans, J P Geshuri, D Phelan, M C Schwartz, C E Producer: 19950815 In: Clinical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Synthesis and evaluation of hydroxyproline-derived isoprenyltransferase inhibitors. [electronic resource] by O'Connell, C E Ackermann, K Rowell, C A Garcia, A M Lewis, M D Schwartz, C E Producer: 19990924 In: Bioorganic & medicinal chemistry letters vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype. [electronic resource] by Vervoort, V S Viljoen, D Smart, R Suthers, G DuPont, B R Abbott, A Schwartz, C E Producer: 20030312 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Allan-Herndon syndrome. I. Clinical studies. [electronic resource] by Stevenson, R E Goodman, H O Schwartz, C E Simensen, R J McLean, W T Herndon, C N Producer: 19900928 In: American journal of human genetics vol. 47 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 193 results.