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J A Goodship

Showing results (1-10 of 34) with videos related to

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Molecular Medicine Today|January 27, 2000
UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotypeJ A Goodship, J Burn
American Journal of Medical Genetics|October 23, 1997
Another case of maternal uniparental disomy chromosome 14 syndromeM P Splitt, J A Goodship
The New England Journal of Medicine|May 1, 1999
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndromeP Warwicker, J A Goodship, T H Goodship
Immunogenetics|September 1, 1997
Three new polymorphisms in the human complement factor H gene and promoter regionP Warwicker, T H Goodship, J A Goodship
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 27, 1998
Factor H--US?P Warwicker, J A Goodship, T H Goodship
Archives of Disease in Childhood|October 1, 1992
Centiles for adult head circumferenceK M Bushby, T Cole, J N Matthews, et al.
Prenatal Diagnosis|December 1, 1992
Prenatal detection of multiple copies of a familial supernumerary marker chromosomeJ Wolstenholme, J A Brummitt, C J English, et al.
Heart (British Cardiac Society)|April 1, 1997
Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxyM Penman Splitt, M Y Tsai, J Burn, et al.
Bioinformatics (Oxford, England)|February 15, 2011
Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genomeK J Siddle, J A Goodship, B Keavney, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 12 mosaicism in a 7 year old girl with dysmorphic features and normal mental developmentC J English, J A Goodship, A Jackson, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Molecular Medicine Today|January 27, 2000
UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotypeJ A Goodship, J Burn
American Journal of Medical Genetics|October 23, 1997
Another case of maternal uniparental disomy chromosome 14 syndromeM P Splitt, J A Goodship
The New England Journal of Medicine|May 1, 1999
von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndromeP Warwicker, J A Goodship, T H Goodship
Immunogenetics|September 1, 1997
Three new polymorphisms in the human complement factor H gene and promoter regionP Warwicker, T H Goodship, J A Goodship
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 27, 1998
Factor H--US?P Warwicker, J A Goodship, T H Goodship
Archives of Disease in Childhood|October 1, 1992
Centiles for adult head circumferenceK M Bushby, T Cole, J N Matthews, et al.
Prenatal Diagnosis|December 1, 1992
Prenatal detection of multiple copies of a familial supernumerary marker chromosomeJ Wolstenholme, J A Brummitt, C J English, et al.
Heart (British Cardiac Society)|April 1, 1997
Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxyM Penman Splitt, M Y Tsai, J Burn, et al.
Bioinformatics (Oxford, England)|February 15, 2011
Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genomeK J Siddle, J A Goodship, B Keavney, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 12 mosaicism in a 7 year old girl with dysmorphic features and normal mental developmentC J English, J A Goodship, A Jackson, et al.
Pageof 4