Correction: Two ENU-Induced Alleles of Atp2b2 Cause Deafness in Mice

af Carpinelli, Marina R., Manning, Michael G., Kile, Benjamin T., Burt, Rachel A.
Udgivet 2013

Organotypic Culture of Neonatal Murine Inner Ear Explants

af Ogier, Jacqueline M., Burt, Rachel A., Drury, Hannah R., Lim, Rebecca, Nayagam, Bryony A.
Udgivet i Front Cell Neurosci (2019)

CHD7 Deficiency in “Looper”, a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment

af Ogier, Jacqueline M., Carpinelli, Marina R., Arhatari, Benedicta D., Symons, R. C. Andrew, Kile, Benjamin T., Burt, Rachel A.
Udgivet 2014

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome

af Ogier, Jacqueline M., Arhatari, Benedicta D., Carpinelli, Marina R., McColl, Bradley K., Wilson, Michael A., Burt, Rachel A.
Udgivet i Sci Rep (2018)

A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination

af Carpinelli, Marina R., Voss, Anne K., Manning, Michael G., Perera, Ashwyn A., Cooray, Anne A., Kile, Benjamin T., Burt, Rachel A.
Udgivet 2014

Mice That Are Congenic for the char2 Locus Are Susceptible to Malaria

af Burt, Rachel A., Marshall, Vikki M., Wagglen, Jamie, Rodda, Fleur R., Senyschen, Danielle, Baldwin, Tracey M., Buckingham, Lynn A., Foote, Simon J.
Udgivet 2002

Antibodies against Merozoite Surface Protein (Msp)-1(19) Are a Major Component of the Invasion-Inhibitory Response in Individuals Immune to Malaria

af O'Donnell, Rebecca A., de Koning-Ward, Tania F., Burt, Rachel A., Bockarie, Moses, Reeder, John C., Cowman, Alan F., Crabb, Brendan S.
Udgivet 2001

Genomewide Scan in Families with Schizophrenia from the Founder Population of Afrikaners Reveals Evidence for Linkage and Uniparental Disomy on Chromosome 1

af Abecasis, Gonçalo R., Burt, Rachel A., Hall, Diana, Bochum, Sylvia, Doheny, Kimberly F., Lundy, S. Laura, Torrington, Marie, Roos, J. Louw, Gogos, Joseph A., Karayiorgou, Maria
Udgivet 2004

A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort

af Downie, Lilian, Halliday, Jane L, Burt, Rachel A, Lunke, Sebastian, Lynch, Elly, Martyn, Melissa, Poulakis, Zeffie, Gaff, Clara, Sung, Valerie, Wake, Melissa, Hunter, Matthew, Saunders, Kerryn, Rose, Elizabeth, Rehm, Heidi L, Amor, David J
Udgivet i BMJ Paediatr Open (2017)