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	1.	Less is more: compact genomes pay dividends. [electronic resource] by Angrist, M Producer: 19990305 In: Genome research vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Does phaster mean better? [electronic resource] by Angrist, M Producer: 19970328 In: Clinical chemistry vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	3.	Living laboratory: whole-genome sequencing as a learning healthcare enterprise. [electronic resource] by Angrist, M Jamal, L Producer: 20151215 In: Clinical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Autism resources at the higher education level in Indiana. [electronic resource] by Dalrymple, N J Angrist, M H Producer: 19890601 In: Journal of autism and developmental disorders vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA. [electronic resource] by Angrist, M Wells, D E Chakravarti, A Pandey, A Producer: 19970206 In: Genomics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient. [electronic resource] by Angrist, M Bolk, S Halushka, M Lapchak, P A Chakravarti, A Producer: 19961216 In: Nature genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease. [electronic resource] by Angrist, M Bolk, S Bentley, K Nallasamy, S Halushka, M K Chakravarti, A Producer: 19990125 In: Oncogene vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET. [electronic resource] by Bolk, S Angrist, M Schwartz, S Silvestri, J M Weese-Mayer, D E Chakravarti, A Producer: 19970320 In: American journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR. [electronic resource] by Chadwick, B P Helbling, L A Angrist, M Chakravarti, A Gusella, J F Slaugenhaupt, S A Producer: 19990330 In: Cytogenetics and cell genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome. [electronic resource] by Bolk, S Angrist, M Xie, J Yanagisawa, M Silvestri, J M Weese-Mayer, D E Chakravarti, A Producer: 19960905 In: Nature genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility. [electronic resource] by Angrist, M Jing, S Bolk, S Bentley, K Nallasamy, S Halushka, M Fox, G M Chakravarti, A Producer: 19980608 In: Genomics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT. [electronic resource] by Davis, E E Savage, J H Willer, J R Jiang, Y-H Angrist, M Androutsopoulos, A Katsanis, N Producer: 20150512 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome. [electronic resource] by Southard-Smith, E M Angrist, M Ellison, J S Agarwala, R Baxevanis, A D Chakravarti, A Pavan, W J Producer: 19990618 In: Genome research vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	14.	Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease. [electronic resource] by Angrist, M Bolk, S Thiel, B Puffenberger, E G Hofstra, R M Buys, C H Cass, D T Chakravarti, A Producer: 19950914 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus. [electronic resource] by Bolk, S Pelet, A Hofstra, R M Angrist, M Salomon, R Croaker, D Buys, C H Lyonnet, S Chakravarti, A Producer: 20000210 In: Proceedings of the National Academy of Sciences of the United States of America vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. [electronic resource] by Hentati, A Pericak-Vance, M A Lennon, F Wasserman, B Hentati, F Juneja, T Angrist, M H Hung, W Y Boustany, R M Bohlega, S Producer: 19950316 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. [electronic resource] by Puffenberger, E G Kauffman, E R Bolk, S Matise, T C Washington, S S Angrist, M Weissenbach, J Garver, K L Mascari, M Ladda, R Producer: 19950110 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. [electronic resource] by Angrist, M Kauffman, E Slaugenhaupt, S A Matise, T C Puffenberger, E G Washington, S S Lipson, A Cass, D T Reyna, T Weeks, D E Producer: 19931105 In: Nature genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome). [electronic resource] by Hofstra, R M Osinga, J Tan-Sindhunata, G Wu, Y Kamsteeg, E J Stulp, R P van Ravenswaaij-Arts, C Majoor-Krakauer, D Angrist, M Chakravarti, A Meijers, C Buys, C H Producer: 19960703 In: Nature genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)