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L J Logie

Showing results (1-10 of 6) with videos related to

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Archives of Disease in Childhood|January 6, 1999
Intelligence and development in Aarskog syndromeL J Logie, M E Porteous
Molecular Genetics and Metabolism|May 3, 2005
Calpain inhibition and insulin action in cultured human muscle cellsL J Logie, A E Brown, S J Yeaman, et al.
Journal of Medical Genetics|May 23, 1998
Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2M E Porteous, L Strain, L J Logie, et al.
Human Molecular Genetics|February 1, 1994
Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15-21 in Marfan syndrome patientsC Hayward, A L Rae, M E Porteous, et al.
Archives of Disease in Childhood|May 1, 1994
Alpha thalassaemia mental retardation (ATR-X): an atypical familyL J Logie, R J Gibbons, D R Higgs, et al.
Cell|November 18, 1994
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factorN G Pasteris, A Cadle, L J Logie, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Archives of Disease in Childhood|January 6, 1999
Intelligence and development in Aarskog syndromeL J Logie, M E Porteous
Molecular Genetics and Metabolism|May 3, 2005
Calpain inhibition and insulin action in cultured human muscle cellsL J Logie, A E Brown, S J Yeaman, et al.
Journal of Medical Genetics|May 23, 1998
Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2M E Porteous, L Strain, L J Logie, et al.
Human Molecular Genetics|February 1, 1994
Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15-21 in Marfan syndrome patientsC Hayward, A L Rae, M E Porteous, et al.
Archives of Disease in Childhood|May 1, 1994
Alpha thalassaemia mental retardation (ATR-X): an atypical familyL J Logie, R J Gibbons, D R Higgs, et al.
Cell|November 18, 1994
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factorN G Pasteris, A Cadle, L J Logie, et al.
Pageof 1