Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10

Por Zheng, Qing Yin, Harris, Belinda S, Ward-Bailey, Patricia F, Yu, Heping, Bronson, Roderick T, Davisson, Muriel T, Johnson, Kenneth R
Publicado em 2004

A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis

Por DONAHUE, LEAH RAE, CHANG, BO, MOHAN, SUBBURAMAN, MIYAKOSHI, NAO, WERGEDAL, JON E, BAYLINK, DAVID J, HAWES, NORMAN L, ROSEN, CLIFFORD J, WARD-BAILEY, PATRICIA, ZHENG, QING Y, BRONSON, RODERICK T, JOHNSON, KENNETH R, DAVISSON, MURIEL T
Publicado em 2003

Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders

Por Fairfield, Heather, Srivastava, Anuj, Ananda, Guruprasad, Liu, Rangjiao, Kircher, Martin, Lakshminarayana, Anuradha, Harris, Belinda S., Karst, Son Yong, Dionne, Louise A., Kane, Coleen C., Curtain, Michelle, Berry, Melissa L., Ward-Bailey, Patricia F., Greenstein, Ian, Byers, Candice, Czechanski, Anne, Sharp, Jocelyn, Palmer, Kristina, Gudis, Polyxeni, Martin, Whitney, Tadenev, Abby, Bogdanik, Laurent, Pratt, C. Herbert, Chang, Bo, Schroeder, David G., Cox, Gregory A., Cliften, Paul, Milbrandt, Jeffrey, Murray, Stephen, Burgess, Robert, Bergstrom, David E., Donahue, Leah Rae, Hamamy, Hanan, Masri, Amira, Santoni, Federico A., Makrythanasis, Periklis, Antonarakis, Stylianos E., Shendure, Jay, Reinholdt, Laura G.
Publicado no Genome Res (2015)