Your search returned 16 results.

Results
	1.	Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25. [electronic resource] by Gould, D B Mears, A J Pearce, W G Walter, M A Producer: 19971022 In: American journal of human genetics vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	2.	Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct. [electronic resource] by Walter, M A Mirzayans, F Mears, A J Hickey, K Pearce, W G Producer: 19961220 In: Ophthalmology vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25. [electronic resource] by Mears, A J Mirzayans, F Gould, D B Pearce, W G Walter, M A Producer: 19970114 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	4.	Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22. [electronic resource] by Dawson, A J Mears, A J Chudley, A E Bech-Hansen, T McDermid, H Producer: 19970313 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning. [electronic resource] by Mirzayans, F Mears, A J Guo, S W Pearce, W G Walter, M A Producer: 19970826 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)
	6.	Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. [electronic resource] by Mears, A J el-Shanti, H Murray, J C McDermid, H E Patil, S R Producer: 19951012 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	7.	The E subunit of vacuolar H(+)-ATPase localizes close to the centromere on human chromosome 22. [electronic resource] by Baud, V Mears, A J Lamour, V Scamps, C Duncan, A M McDermid, H E Lipinski, M Producer: 19940718 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Mining the transcriptome for rare disease therapies: a comparison of the efficiencies of two data mining approaches and a targeted cell-based drug screen. [electronic resource] by Mears, A J Schock, S C Hadwen, J Putos, S Dyment, D Boycott, K M MacKenzie, Alex Publication details: NPJ genomic medicine 2017 In: NPJ genomic medicine vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25. [electronic resource] by Mirzayans, F Gould, D B Héon, E Billingsley, G D Cheung, J C Mears, A J Walter, M A Producer: 20000414 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)
	10.	From disease genes to cellular pathways: a progress report. [electronic resource] by Yu, J Mears, A J Yoshida, S Farjo, R Carter, T A Ghosh, D Hero, A Barlow, C Swaroop, A Producer: 20040304 In: Novartis Foundation symposium vol. 255 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Nrl is required for rod photoreceptor development. [electronic resource] by Mears, A J Kondo, M Swain, P K Takada, Y Bush, R A Saunders, T L Sieving, P A Swaroop, A Producer: 20011220 In: Nature genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa. [electronic resource] by Mears, A J Gieser, L Yan, D Chen, C Fahrner, S Hiriyanna, S Fujita, R Jacobson, S G Sieving, P A Swaroop, A 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)
	13.	Molecular characterization of the marker chromosome associated with cat eye syndrome. [electronic resource] by Mears, A J Duncan, A M Budarf, M L Emanuel, B S Sellinger, B Siegel-Bartelt, J Greenberg, C R McDermid, H E Producer: 19940729 In: American journal of human genetics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	14.	Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptors. [electronic resource] by Swain, P K Hicks, D Mears, A J Apel, I J Smith, J E John, S K Hendrickson, A Milam, A H Swaroop, A Producer: 20011101 In: The Journal of biological chemistry vol. 276 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15. [electronic resource] by Mears, A J Hiriyanna, S Vervoort, R Yashar, B Gieser, L Fahrner, S Daiger, S P Heckenlively, J R Sieving, P A Wright, A F Swaroop, A Producer: 20001031 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly. [electronic resource] by Mears, A J Jordan, T Mirzayans, F Dubois, S Kume, T Parlee, M Ritch, R Koop, B Kuo, W L Collins, C Marshall, J Gould, D B Pearce, W Carlsson, P Enerbäck, S Morissette, J Bhattacharya, S Hogan, B Raymond, V Walter, M A Producer: 19981223 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)