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J J Jonsson

Showing results (11-20 of 15) with videos related to

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Human Gene Therapy|February 10, 1996
Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II)S E Braun, D Pan, E L Aronovich, et al.
Familial Cancer|September 26, 2018
Electronically ascertained extended pedigrees in breast cancer genetic counselingV Stefansdottir, H Skirton, O Th Johannsson, et al.
Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.
Lipids|August 21, 2007
Positive association between plasma antioxidant capacity and n-3 PUFA in red blood cells from womenA Y Thorlaksdottir, G V Skuladottir, A L Petursdottir, et al.
Journal of Medical Genetics|May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?J J Jonsson, A Renieri, P G Gallagher, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Human Gene Therapy|February 10, 1996
Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II)S E Braun, D Pan, E L Aronovich, et al.
Familial Cancer|September 26, 2018
Electronically ascertained extended pedigrees in breast cancer genetic counselingV Stefansdottir, H Skirton, O Th Johannsson, et al.
Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.
Lipids|August 21, 2007
Positive association between plasma antioxidant capacity and n-3 PUFA in red blood cells from womenA Y Thorlaksdottir, G V Skuladottir, A L Petursdottir, et al.
Journal of Medical Genetics|May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?J J Jonsson, A Renieri, P G Gallagher, et al.
Pageof 2