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H Firth

Showing results (41-50 of 46) with videos related to

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Journal of Medical Genetics|August 6, 2002
Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practiceD J Halliday, S Hutchinson, L Lonie, et al.
Veterinary and Human Toxicology|June 4, 1998
Client satisfaction with the New Zealand National Poisons Information ServiceS Cameron, B Cheu, J Green, et al.
Clinical and Experimental Immunology|July 9, 2020
Primary pneumococcal peritonitis can be the first presentation of a familial complement factor I deficiency<sup>1</sup>S Ugrinovic, H Firth, D Kavanagh, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.
Journal of Medical Genetics|April 5, 2005
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndromeK Tatton-Brown, J Douglas, K Coleman, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Journal of Medical Genetics|August 6, 2002
Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practiceD J Halliday, S Hutchinson, L Lonie, et al.
Veterinary and Human Toxicology|June 4, 1998
Client satisfaction with the New Zealand National Poisons Information ServiceS Cameron, B Cheu, J Green, et al.
Clinical and Experimental Immunology|July 9, 2020
Primary pneumococcal peritonitis can be the first presentation of a familial complement factor I deficiency<sup>1</sup>S Ugrinovic, H Firth, D Kavanagh, et al.
Journal of Medical Genetics|April 3, 2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic featuresC Shaw-Smith, R Redon, L Rickman, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.
Journal of Medical Genetics|April 5, 2005
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndromeK Tatton-Brown, J Douglas, K Coleman, et al.
Pageof 5