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	101.	Xeroderma pigmentosum: a rapid sensitive method for prenatal diagnosis. [electronic resource] by Regan, J D Setlow, R B Kaback, M M Howell, R R Klein, E Burgess, G Producer: 19720125 In: Science (New York, N.Y.) vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Ganglioside GM2 levels in human melanoma cells: inverse correlation with lysosomal beta-hexosaminidase A activity. [electronic resource] by Hoon, D S Kaback, M M Lim-Steele, J Tsuchida, T Morton, D L Irie, R F Producer: 19920916 In: Biochemistry international vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	103.	Regional mapping of ADA and ITP on human chromosome 20: cytogenetic and somatic cell studies in an X/20 translocation. [electronic resource] by Mohandas, T Sparkes, R S Passage, M B Sparkes, M C Miles, J H Kaback, M M Producer: 19800726 In: Cytogenetics and cell genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Chromosomal mosaicism in amniotic cell culture. A diagnostic Dilemma. [electronic resource] by Kohn, G Mennuti, M T Kaback, M Schwartz, R M Chemke, J Goldman, B Mellman, W J Producer: 19751205 In: Israel journal of medical sciences vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	105.	Second-trimester fetoscopy and fetal blood sampling: current limitations and problems. [electronic resource] by Levine, M D McNeil, D E Kaback, M M Frazer, R E Okada, D M Hobel, C J Producer: 19750122 In: American journal of obstetrics and gynecology vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. [electronic resource] by Struewing, J P Abeliovich, D Peretz, T Avishai, N Kaback, M M Collins, F S Brody, L C Producer: 19951102 In: Nature genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Sampling the fetoplacental circulation. III. Combined laparoscopy-fetoscopy in the pregnant macaque for hemoglobin identification. [electronic resource] by Davidson, E C Morris, J A O'Grady, J P Hendrickx, A G Anderson, J Kaback, M Frazer, R Producer: 19790324 In: American journal of obstetrics and gynecology vol. 132 Availability: No items available. Save to lists Add to cart (remove)
	108.	Letter: Phenotypic variation in alpha-L-iduronidase deficiency. [electronic resource] by Leisti, J Rimoin, D L Kaback, M M Hollister, D W DEn Tandt, W Neufeld, E Matalon, R Philippart, M Producer: 19750918 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy. [electronic resource] by Stevens, R L Fluharty, A L Kihara, H Kaback, M M Shapiro, L J Marsh, B Sandhoff, K Fischer, G Producer: 19820313 In: American journal of human genetics vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	110.	A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimation. [electronic resource] by Cao, Z Natowicz, M R Kaback, M M Lim-Steele, J S Prence, E M Brown, D Chabot, T Triggs-Raine, B L Producer: 19931230 In: American journal of human genetics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	111.	Metachromatic leukodystrophy without arylsulfatase A deficiency. [electronic resource] by Shapiro, L J Aleck, K A Kaback, M M Itabashi, H Desnick, R J Brand, N Stevens, R L Fluharty, A L Kihara, H Producer: 19800128 In: Pediatric research vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British Isles. [electronic resource] by Landels, E C Green, P M Ellis, I H Fensom, A H Kaback, M M Lim-Steele, J Zeiger, K Levy, N Bobrow, M Producer: 19930810 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin. [electronic resource] by Petersen, G M Rotter, J I Cantor, R M Field, L L Greenwald, S Lim, J S Roy, C Schoenfeld, V Lowden, J A Kaback, M M Producer: 19840107 In: American journal of human genetics vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	114.	The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. [electronic resource] by Oddoux, C Struewing, J P Clayton, C M Neuhausen, S Brody, L C Kaback, M Haas, B Norton, L Borgen, P Jhanwar, S Goldgar, D Ostrer, H Offit, K Producer: 19961112 In: Nature genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studies. [electronic resource] by Akerman, B R Zielenski, J Triggs-Raine, B L Prence, E M Natowicz, M R Lim-Steele, J S Kaback, M M Mules, E H Thomas, G H Clarke, J T Producer: 19930610 In: Human mutation vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening. [electronic resource] by Triggs-Raine, B L Mules, E H Kaback, M M Lim-Steele, J S Dowling, C E Akerman, B R Natowicz, M R Grebner, E E Navon, R Welch, J P Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	117.	A Pst+ polymorphism in the HEXA gene with an unusual geographic distribution. [electronic resource] by Kaplan, F Kapoor, S Lee, D Fernandes, M Vienozinskis, M Mascisch, A Scriver, C R Lim-Steele, J Kaback, M Zeiger, K Zoossman-Diskin, A Bonne-Tamir, B Landels, E Bobrow, M Hechtman, P Producer: 19941013 In: European journal of human genetics : EJHG vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics. [electronic resource] by Curry, C J Stevenson, R E Aughton, D Byrne, J Carey, J C Cassidy, S Cunniff, C Graham, J M Jones, M C Kaback, M M Moeschler, J Schaefer, G B Schwartz, S Tarleton, J Opitz, J Producer: 19971218 In: American journal of medical genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	The APCI1307K allele and breast cancer risk. [electronic resource] by Redston, M Nathanson, K L Yuan, Z Q Neuhausen, S L Satagopan, J Wong, N Yang, D Nafa, D Abrahamson, J Ozcelik, H Antin-Ozerkis, D Andrulis, I Daly, M Pinsky, L Schrag, D Gallinger, S Kaback, M King, M C Woodage, T Brody, L C Godwin, A Warner, E Weber, B Foulkes, W Offit, K Producer: 19981022 In: Nature genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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