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J Goodship

Showing results (11-20 of 137) with videos related to

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Journal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.
Lancet (London, England)|August 10, 1999
Left-isomerism sequence and maternal type-1 diabetesM Splitt, C Wright, D Sen, et al.
British Medical Bulletin|September 14, 2006
Atypical haemolytic uraemic syndromeDavid Kavanagh, Timothy H J Goodship, Anna Richards
Archives of Disease in Childhood|January 6, 1999
A population study of chromosome 22q11 deletions in infancyJ Goodship, I Cross, J LiLing, et al.
Journal of Medical Genetics|October 1, 1991
A male with type I orofaciodigital syndromeJ Goodship, J Platt, R Smith, et al.
Journal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.
Current Opinion in Nephrology and Hypertension|July 10, 2002
The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpuraAnna Richards, Judith A Goodship, Timothy H J Goodship
Journal of Medical Genetics|March 1, 1988
Intellectual development in Apert's syndrome: a long term follow up of 29 patientsM A Patton, J Goodship, R Hayward, et al.
Pediatric Nephrology (Berlin, Germany)|May 17, 2008
Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutationJean Claude Davin, Lisa Strain, Tim H J Goodship
Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.
Pageof 14

Showing results (11-20 of 137) with videos related to

Sort By:
Pageof 14
Journal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.
Lancet (London, England)|August 10, 1999
Left-isomerism sequence and maternal type-1 diabetesM Splitt, C Wright, D Sen, et al.
British Medical Bulletin|September 14, 2006
Atypical haemolytic uraemic syndromeDavid Kavanagh, Timothy H J Goodship, Anna Richards
Archives of Disease in Childhood|January 6, 1999
A population study of chromosome 22q11 deletions in infancyJ Goodship, I Cross, J LiLing, et al.
Journal of Medical Genetics|October 1, 1991
A male with type I orofaciodigital syndromeJ Goodship, J Platt, R Smith, et al.
Journal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.
Current Opinion in Nephrology and Hypertension|July 10, 2002
The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpuraAnna Richards, Judith A Goodship, Timothy H J Goodship
Journal of Medical Genetics|March 1, 1988
Intellectual development in Apert's syndrome: a long term follow up of 29 patientsM A Patton, J Goodship, R Hayward, et al.
Pediatric Nephrology (Berlin, Germany)|May 17, 2008
Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutationJean Claude Davin, Lisa Strain, Tim H J Goodship
Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.
Pageof 14