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Trent Burgess

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American Journal of Medical Genetics. Part A|August 14, 2012
Phenotype in novel Xp duplicationManju Salaria, Trent Burgess, Stella Setyapranata, et al.
The Journal of Pediatrics|November 1, 2013
The prevalence of turner syndrome in girls presenting with coarctation of the aortaSze Choong Wong, Trent Burgess, Michael Cheung, et al.
Clinical Case Reports|March 9, 2019
A novel familial 9q31.2q32 microdeletion: Muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short statureAnand K Ramineni, Trent Burgess, Penny Cruickshanks, et al.
Molecular Cytogenetics|May 13, 2008
An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)Mahmoud S Khaniani, Paul Kalitsis, Trent Burgess, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Questionable pathogenicity of FOXG1 duplicationDavid J Amor, Trent Burgess, Tiong Y Tan, et al.
Gene|July 9, 2013
Neonatal presentation of chromosome 9q33.2-q34.3 duplicationAlexandra Moody, Sam E Athikarisamy, Alison Yeung, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7Zornitza Stark, Monique M Ryan, Damien L Bruno, et al.
European Journal of Human Genetics : EJHG|November 17, 2016
Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practiceJean Lillian Paul, Rachel Pope-Couston, Samantha Wake, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
5q31.3 Microdeletion syndrome: clinical and molecular characterization of two further casesNatasha Brown, Trent Burgess, Robin Forbes, et al.
Case Reports in Genetics|March 21, 2014
Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureTrent Burgess, Lilian Downie, Mark D Pertile, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|August 14, 2012
Phenotype in novel Xp duplicationManju Salaria, Trent Burgess, Stella Setyapranata, et al.
The Journal of Pediatrics|November 1, 2013
The prevalence of turner syndrome in girls presenting with coarctation of the aortaSze Choong Wong, Trent Burgess, Michael Cheung, et al.
Clinical Case Reports|March 9, 2019
A novel familial 9q31.2q32 microdeletion: Muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short statureAnand K Ramineni, Trent Burgess, Penny Cruickshanks, et al.
Molecular Cytogenetics|May 13, 2008
An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)Mahmoud S Khaniani, Paul Kalitsis, Trent Burgess, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Questionable pathogenicity of FOXG1 duplicationDavid J Amor, Trent Burgess, Tiong Y Tan, et al.
Gene|July 9, 2013
Neonatal presentation of chromosome 9q33.2-q34.3 duplicationAlexandra Moody, Sam E Athikarisamy, Alison Yeung, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7Zornitza Stark, Monique M Ryan, Damien L Bruno, et al.
European Journal of Human Genetics : EJHG|November 17, 2016
Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practiceJean Lillian Paul, Rachel Pope-Couston, Samantha Wake, et al.
American Journal of Medical Genetics. Part A|August 17, 2013
5q31.3 Microdeletion syndrome: clinical and molecular characterization of two further casesNatasha Brown, Trent Burgess, Robin Forbes, et al.
Case Reports in Genetics|March 21, 2014
Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureTrent Burgess, Lilian Downie, Mark D Pertile, et al.
Pageof 5