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L Bason

Showing results (1-10 of 7) with videos related to

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American Journal of Medical Genetics|February 5, 1998
Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalusJ S Du, L Bason, H Woffendin, et al.
Analytical Biochemistry|August 15, 1992
Same-day batch measurement of glycine betaine, carnitine, and other betaines in biological materialM Lever, L Bason, C Leaver, et al.
Biochemistry|September 28, 1993
Reporter epitopes: a novel approach to examine transmembrane topology of integral membrane proteins applied to the alpha 1 subunit of the nicotinic acetylcholine receptorR Anand, L Bason, M S Saedi, et al.
Journal of Medical Genetics|December 20, 2003
Consequences of JAG1 mutationsB M Kamath, L Bason, D A Piccoli, et al.
Human Mutation|February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patientsR P Colliton, L Bason, F M Lu, et al.
Clinical Genetics|July 18, 2002
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing lossL Bason, T Dudley, K Lewis, et al.
American Journal of Medical Genetics|October 23, 1995
Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletionD M McDonald-McGinn, D A Driscoll, L Bason, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|February 5, 1998
Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalusJ S Du, L Bason, H Woffendin, et al.
Analytical Biochemistry|August 15, 1992
Same-day batch measurement of glycine betaine, carnitine, and other betaines in biological materialM Lever, L Bason, C Leaver, et al.
Biochemistry|September 28, 1993
Reporter epitopes: a novel approach to examine transmembrane topology of integral membrane proteins applied to the alpha 1 subunit of the nicotinic acetylcholine receptorR Anand, L Bason, M S Saedi, et al.
Journal of Medical Genetics|December 20, 2003
Consequences of JAG1 mutationsB M Kamath, L Bason, D A Piccoli, et al.
Human Mutation|February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patientsR P Colliton, L Bason, F M Lu, et al.
Clinical Genetics|July 18, 2002
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing lossL Bason, T Dudley, K Lewis, et al.
American Journal of Medical Genetics|October 23, 1995
Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletionD M McDonald-McGinn, D A Driscoll, L Bason, et al.
Pageof 1