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K J Matteson

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Proceedings of the National Academy of Sciences of the United States of America|December 1, 1986
Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placentaB C Chung, K J Matteson, R Voutilainen, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1986
Assignment of the gene for adrenal P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase) to human chromosome 10K J Matteson, J Picado-Leonard, B C Chung, et al.
The Journal of Pediatrics|September 1, 1992
Use of a molecular genetic approach to diagnosing the fragile X genotypeN T Potter, C B Lozzio, I J Anderson, et al.
Annals of the New York Academy of Sciences|January 1, 1985
An approach to the molecular biology of congenital adrenal hyperplasiaB C Chung, K J Matteson, J E Morin, et al.
Rapid Communications in Mass Spectrometry : RCM|January 1, 1995
Detection of delta F508 mutation of the cystic fibrosis gene by matrix-assisted laser desorption/ionization mass spectrometryL Y Ch'ang, K Tang, M Schell, et al.
American Journal of Human Genetics|January 1, 1990
Regional evaluation of DNA diagnostic laboratoriesK J Matteson, P E Barker, G C Kaplan, et al.
Human Genetics|January 1, 1985
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locusK J Matteson, H Ostrer, A Chakravarti, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasiaK J Matteson, J A Phillips, W L Miller, et al.
Genetic Analysis : Biomolecular Engineering|October 1, 1996
Laser desorption mass spectrometry for point mutation detectionN I Taranenko, K J Matteson, C N Chung, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1986
Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placentaB C Chung, K J Matteson, R Voutilainen, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1986
Assignment of the gene for adrenal P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase) to human chromosome 10K J Matteson, J Picado-Leonard, B C Chung, et al.
The Journal of Pediatrics|September 1, 1992
Use of a molecular genetic approach to diagnosing the fragile X genotypeN T Potter, C B Lozzio, I J Anderson, et al.
Annals of the New York Academy of Sciences|January 1, 1985
An approach to the molecular biology of congenital adrenal hyperplasiaB C Chung, K J Matteson, J E Morin, et al.
Rapid Communications in Mass Spectrometry : RCM|January 1, 1995
Detection of delta F508 mutation of the cystic fibrosis gene by matrix-assisted laser desorption/ionization mass spectrometryL Y Ch'ang, K Tang, M Schell, et al.
American Journal of Human Genetics|January 1, 1990
Regional evaluation of DNA diagnostic laboratoriesK J Matteson, P E Barker, G C Kaplan, et al.
Human Genetics|January 1, 1985
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locusK J Matteson, H Ostrer, A Chakravarti, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasiaK J Matteson, J A Phillips, W L Miller, et al.
Genetic Analysis : Biomolecular Engineering|October 1, 1996
Laser desorption mass spectrometry for point mutation detectionN I Taranenko, K J Matteson, C N Chung, et al.
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