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V Morgan

Showing results (231-240 of 278) with videos related to

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The New England Journal of Medicine|August 4, 2001
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasiaR C Trembath, J R Thomson, R D Machado, et al.
Journal of Medical Genetics|June 17, 2003
A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13N V Morgan, C Bacchelli, P Gissen, et al.
Frontiers in Science|December 11, 2025
Precision cardiovascular medicine: shifting the innovation paradigmMasanori Aikawa, Abhijeet R Sonawane, Sarvesh Chelvanambi, et al.
Blood|October 9, 2013
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defectsJacqueline Stockley, Neil V Morgan, Danai Bem, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
Blood|January 11, 2014
Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assayMarie Lordkipanidzé, Gillian C Lowe, Nicholas S Kirkby, et al.
Cancer Research|February 28, 2001
Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regionsA M Cleton-Jansen, D F Callen, R Seshadri, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
Communications Earth & Environment|June 12, 2026
A long-lived impact-generated hydrothermal system at the Chicxulub impact structureAnnemarie E Pickersgill, Evangelos Christou, Marissa M Tremblay, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Pageof 28

Showing results (231-240 of 278) with videos related to

Sort By:
Pageof 28
The New England Journal of Medicine|August 4, 2001
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasiaR C Trembath, J R Thomson, R D Machado, et al.
Journal of Medical Genetics|June 17, 2003
A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13N V Morgan, C Bacchelli, P Gissen, et al.
Frontiers in Science|December 11, 2025
Precision cardiovascular medicine: shifting the innovation paradigmMasanori Aikawa, Abhijeet R Sonawane, Sarvesh Chelvanambi, et al.
Blood|October 9, 2013
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defectsJacqueline Stockley, Neil V Morgan, Danai Bem, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9I Demuth, M Wlodarski, A J Tipping, et al.
Blood|January 11, 2014
Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assayMarie Lordkipanidzé, Gillian C Lowe, Nicholas S Kirkby, et al.
Cancer Research|February 28, 2001
Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regionsA M Cleton-Jansen, D F Callen, R Seshadri, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
Communications Earth & Environment|June 12, 2026
A long-lived impact-generated hydrothermal system at the Chicxulub impact structureAnnemarie E Pickersgill, Evangelos Christou, Marissa M Tremblay, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Pageof 28