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Shelagh Joss

Showing results (1-10 of 78) with videos related to

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Archives of Disease in Childhood. Education and Practice Edition|February 3, 2019
Transcriptome: from laboratory to clinic roomRebecca Amy Dalrymple, Shelagh Joss
Archives of Disease in Childhood. Education and Practice Edition|January 13, 2021
How to use genetic testing after sudden infant death syndromeLisa Jennifer Bryson, Shelagh Joss
Archives of Disease in Childhood. Education and Practice Edition|September 6, 2014
How to use… microarray comparative genomic hybridisation to investigate developmental disordersMira Kharbanda, John Tolmie, Shelagh Joss
Clinical Dysmorphology|October 29, 2002
A Schinzel-Giedion-like syndrome--a milder version or a separate condition?Shelagh Joss, John C S Dean
Clinical Dysmorphology|March 14, 2007
Nasopharyngeal teratoma associated with a complex congenital cardiac anomalySumita P Saha, Emma Hobson, Shelagh Joss
Archives of Disease in Childhood|September 28, 2014
Chromosomal microarray analysis for looked after children: a double-edged sword?Mark James Hamilton, John Lorimer Tolmie, Shelagh Joss, et al.
Clinical Dysmorphology|December 3, 2009
Focal segmental glomerulosclerosis in a female patient with Donnai-Barrow syndromeIhab Sakr Shaheen, Eric Finlay, Katrina Prescott, et al.
European Journal of Medical Genetics|January 5, 2011
The face of Ulnar Mammary syndrome?Shelagh Joss, Usha Kini, Richard Fisher, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Mardini-Nyhan association (lung agenesis, congenital heart, and thumb anomalies): three new cases and possible recurrence in a sib-is there a distinct recessive syndrome?Rob Hastings, David Harding, Alan Donaldson, et al.
Clinical Genetics|March 21, 2012
Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?Ruth McGowan, Benjamin R Challoner, Sarah Ross, et al.
Pageof 8

Showing results (1-10 of 78) with videos related to

Sort By:
Pageof 8
Archives of Disease in Childhood. Education and Practice Edition|February 3, 2019
Transcriptome: from laboratory to clinic roomRebecca Amy Dalrymple, Shelagh Joss
Archives of Disease in Childhood. Education and Practice Edition|January 13, 2021
How to use genetic testing after sudden infant death syndromeLisa Jennifer Bryson, Shelagh Joss
Archives of Disease in Childhood. Education and Practice Edition|September 6, 2014
How to use… microarray comparative genomic hybridisation to investigate developmental disordersMira Kharbanda, John Tolmie, Shelagh Joss
Clinical Dysmorphology|October 29, 2002
A Schinzel-Giedion-like syndrome--a milder version or a separate condition?Shelagh Joss, John C S Dean
Clinical Dysmorphology|March 14, 2007
Nasopharyngeal teratoma associated with a complex congenital cardiac anomalySumita P Saha, Emma Hobson, Shelagh Joss
Archives of Disease in Childhood|September 28, 2014
Chromosomal microarray analysis for looked after children: a double-edged sword?Mark James Hamilton, John Lorimer Tolmie, Shelagh Joss, et al.
Clinical Dysmorphology|December 3, 2009
Focal segmental glomerulosclerosis in a female patient with Donnai-Barrow syndromeIhab Sakr Shaheen, Eric Finlay, Katrina Prescott, et al.
European Journal of Medical Genetics|January 5, 2011
The face of Ulnar Mammary syndrome?Shelagh Joss, Usha Kini, Richard Fisher, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Mardini-Nyhan association (lung agenesis, congenital heart, and thumb anomalies): three new cases and possible recurrence in a sib-is there a distinct recessive syndrome?Rob Hastings, David Harding, Alan Donaldson, et al.
Clinical Genetics|March 21, 2012
Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?Ruth McGowan, Benjamin R Challoner, Sarah Ross, et al.
Pageof 8