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	1.	A bipartite DNA-binding domain in yeast Reb1p. [electronic resource] by Morrow, B E Ju, Q Warner, J R Producer: 19930224 In: Molecular and cellular biology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. [electronic resource] by Edelmann, L Pandita, R K Morrow, B E Producer: 20000405 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11. [electronic resource] by Funke, B Pandita, R K Morrow, B E Producer: 20010906 In: Genomics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Purification and characterization of the yeast rDNA binding protein REB1. [electronic resource] by Morrow, B E Ju, Q Warner, J R Producer: 19910117 In: The Journal of biological chemistry vol. 265 Availability: No items available. Save to lists Add to cart (remove)
	5.	The rRNA enhancer regulates rRNA transcription in Saccharomyces cerevisiae. [electronic resource] by Morrow, B E Johnson, S P Warner, J R Producer: 19930224 In: Molecular and cellular biology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	REB1, a yeast DNA-binding protein with many targets, is essential for growth and bears some resemblance to the oncogene myb. [electronic resource] by Ju, Q D Morrow, B E Warner, J R Producer: 19901018 In: Molecular and cellular biology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Proteins that bind to the yeast rDNA enhancer. [electronic resource] by Morrow, B E Johnson, S P Warner, J R Producer: 19890629 In: The Journal of biological chemistry vol. 264 Availability: No items available. Save to lists Add to cart (remove)
	8.	The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning. [electronic resource] by Fagman, H Liao, J Westerlund, J Andersson, L Morrow, B E Nilsson, M Producer: 20070426 In: Human molecular genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A model for transcription termination by RNA polymerase I. [electronic resource] by Lang, W H Morrow, B E Ju, Q Warner, J R Reeder, R H Producer: 19941220 In: Cell vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome. [electronic resource] by Maldonado-Saldivia, J Funke, B Pandita, R K Schüler, T Morrow, B E Schorle, H Producer: 20001207 In: Mechanisms of development vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	AT-rich palindromes mediate the constitutional t(11;22) translocation. [electronic resource] by Edelmann, L Spiteri, E Koren, K Pulijaal, V Bialer, M G Shanske, A Goldberg, R Morrow, B E Producer: 20010215 In: American journal of human genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus. [electronic resource] by Edelmann, L Stankiewicz, P Spiteri, E Pandita, R K Shaffer, L Lupski, J R Morrow, B E Lupski, J Producer: 20010503 In: Genome research vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11. [electronic resource] by Funke, B Edelmann, L McCain, N Pandita, R K Ferreira, J Merscher, S Zohouri, M Cannizzaro, L Shanske, A Morrow, B E Producer: 19990420 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A common molecular basis for rearrangement disorders on chromosome 22q11. [electronic resource] by Edelmann, L Pandita, R K Spiteri, E Funke, B Goldberg, R Palanisamy, N Chaganti, R S Magenis, E Shprintzen, R J Morrow, B E Producer: 19990816 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11. [electronic resource] by Funke, B Saint-Jore, B Puech, A Sirotkin, H Edelmann, L Carlson, C Raft, S Pandita, R K Kucherlapati, R Skoultchi, A Morrow, B E Producer: 19980309 In: Genomics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Potential mapping of corneal dermoids to Xq24-qter. [electronic resource] by Dar, P Javed, A A Ben-Yishay, M Ferreira, J C Paterson, A D Gross, S J Chitayat, D Morrow, B E Nitowsky, H M Producer: 20020107 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation. [electronic resource] by Edelmann, L Spiteri, E McCain, N Goldberg, R Pandita, R K Duong, S Fox, J Blumenthal, D Lalani, S R Shaffer, L G Morrow, B E Producer: 20000127 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects. [electronic resource] by Funke, B Epstein, J A Kochilas, L K Lu, M M Pandita, R K Liao, J Bauerndistel, R Schüler, T Schorle, H Brown, M C Adams, J Morrow, B E Producer: 20020221 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients. [electronic resource] by Carlson, C Sirotkin, H Pandita, R Goldberg, R McKie, J Wadey, R Patanjali, S R Weissman, S M Anyane-Yeboa, K Warburton, D Scambler, P Shprintzen, R Kucherlapati, R Morrow, B E Producer: 19971022 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome. [electronic resource] by Matsuoka, R Kimura, M Scambler, P J Morrow, B E Imamura, S Minoshima, S Shimizu, N Yamagishi, H Joh-o, K Watanabe, S Oyama, K Saji, T Ando, M Takao, A Momma, K Producer: 19980925 In: Human genetics vol. 103 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 21 results.