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	121.	Familial predisposition to Wilms tumor does not segregate with the WT1 gene. [electronic resource] by Schwartz, C E Haber, D A Stanton, V P Strong, L C Skolnick, M H Housman, D E Producer: 19911104 In: Genomics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients. [electronic resource] by Seranski, P Hoff, C Radelof, U Hennig, S Reinhardt, R Schwartz, C E Heiss, N S Poustka, A Producer: 20010802 In: Gene vol. 270 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Is the E133K allele of VG5Q associated with Klippel-Trenaunay and other overgrowth syndromes? [electronic resource] by Barker, K T Foulkes, W D Schwartz, C E Labadie, C Monsell, F Houlston, R S Harper, J Producer: 20060809 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)
	124.	A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9). [electronic resource] by Ramser, J Winnepenninckx, B Lenski, C Errijgers, V Platzer, M Schwartz, C E Meindl, A Kooy, R F Producer: 20050505 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation. [electronic resource] by Stevenson, R E Häne, B Arena, J F May, M Lawrence, L Lubs, H A Schwartz, C E Producer: 19970822 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	The disruptive behavioral disorder in children and adolescents: comorbidity and clinical course. [electronic resource] by Keller, M B Lavori, P W Beardslee, W R Wunder, J Schwartz, C E Roth, J Biederman, J Producer: 19920521 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)
	127.	Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. [electronic resource] by Willard, H F Waye, J S Skolnick, M H Schwartz, C E Powers, V E England, S B Producer: 19860917 In: Proceedings of the National Academy of Sciences of the United States of America vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene. [electronic resource] by Bock, S C Harris, J F Schwartz, C E Ward, J H Hershgold, E J Skolnick, M H Producer: 19850325 In: American journal of human genetics vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	129.	A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25. [electronic resource] by Cabezas, D A Slaugh, R Abidi, F Arena, J F Stevenson, R E Schwartz, C E Lubs, H A Producer: 20001116 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	The parental origin and mechanism of formation of three dicentric X chromosomes. [electronic resource] by Phelan, M C Prouty, L A Stevenson, R E Howard-Peebles, P N Page, D C Schwartz, C E 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)
	131.	The Hunter-McAlpine syndrome results from duplication 5q35-qter. [electronic resource] by Hunter, A G W Dupont, B McLaughlin, M Hinton, L Baker, E Adès, L Haan, E Schwartz, C E Producer: 20050728 In: Clinical genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58. [electronic resource] by Abidi, F E Holinski-Feder, E Rittinger, O Kooy, F Lubs, H A Stevenson, R E Schwartz, C E Producer: 20020708 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)
	133.	Assessment of diabetes-related distress. [electronic resource] by Polonsky, W H Anderson, B J Lohrer, P A Welch, G Jacobson, A M Aponte, J E Schwartz, C E Producer: 19951121 In: Diabetes care vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28. [electronic resource] by Armfield, K Nelson, R Lubs, H A Häne, B Schroer, R J Arena, F Schwartz, C E Stevenson, R 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)
	135.	Cost-effectiveness of interferon beta-1b in slowing multiple sclerosis disability progression. First estimates. [electronic resource] by Brown, M G Murray, T J Sketris, I S Fisk, J D LeBlanc, J C Schwartz, C E Skedgel, C Producer: 20001207 In: International journal of technology assessment in health care vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. [electronic resource] by Tharapel, A T Anderson, K P Simpson, J L Martens, P R Wilroy, R S Llerena, J C Schwartz, C E Producer: 19930408 In: American journal of human genetics vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	137.	A comparison of two approaches for assessing patient importance weights to conduct an Extended Q-TWiST analysis. [electronic resource] by Schwartz, C E Mathias, S D Pasta, D J Colwell, H H Rapkin, B D Genderson, M W Henning, J M Producer: 19990914 In: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	138.	MRX8: an X-linked mental retardation condition with linkage to Xq21. [electronic resource] by Schwartz, C E May, M Huang, T Ledbetter, D Anderson, G Barker, D F Lubs, H A Arena, F Stevenson, R E 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)
	139.	Fragile X syndrome: linkage analysis in black and white populations. [electronic resource] by Schwartz, C E Phelan, M C Brightharp, C Pancoast, I Howard-Peebles, P N Thibodeau, S Brown, W T Jenkins, E C Producer: 19881108 In: American journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal. [electronic resource] by Marco, E J Abidi, F E Bristow, J Dean, W B Cotter, P Jeremy, R J Schwartz, C E Sherr, E H Producer: 20080312 In: Journal of medical genetics vol. 45 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 193 results.