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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 hydrocephalus
J 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 material
M 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 receptor
R Anand, L Bason, M S Saedi, et al.
Journal of Medical Genetics
|
December 20, 2003
Consequences of JAG1 mutations
B M Kamath, L Bason, D A Piccoli, et al.
Human Mutation
|
February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients
R 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 loss
L 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 deletion
D M McDonald-McGinn, D A Driscoll, L Bason, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 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 hydrocephalus
J 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 material
M 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 receptor
R Anand, L Bason, M S Saedi, et al.
Journal of Medical Genetics
|
December 20, 2003
Consequences of JAG1 mutations
B M Kamath, L Bason, D A Piccoli, et al.
Human Mutation
|
February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients
R 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 loss
L 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 deletion
D M McDonald-McGinn, D A Driscoll, L Bason, et al.
Page
of 1