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Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1986
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster
P S Henthorn, D L Mager, T H Huisman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Localization of two alkaline phosphatase genes to the proximal region of mouse chromosome 1
E Schurr, P S Henthorn, H Harris, et al.
Journal of the American Animal Hospital Association
|
November 14, 1997
X-linked severe combined immunodeficiency in a family of Cardigan Welsh corgis
R P Pullen, R L Somberg, P J Felsburg, et al.
Cell
|
December 1, 1983
Unexpected relationships between four large deletions in the human beta-globin gene cluster
E F Vanin, P S Henthorn, D Kioussis, et al.
The Journal of Biological Chemistry
|
August 25, 1988
Sequence and characterization of the human intestinal alkaline phosphatase gene
P S Henthorn, M Raducha, T Kadesch, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1996
Aberrant properties of alkaline phosphatase in patient fibroblasts correlate with clinical expressivity in severe forms of hypophosphatasia
K N Fedde, M P Michell, P S Henthorn, et al.
Journal of Veterinary Internal Medicine
|
November 7, 2017
Canine GM2-Gangliosidosis Sandhoff Disease Associated with a 3-Base Pair Deletion in the HEXB Gene
P Wang, P S Henthorn, E Galban, et al.
The Journal of Heredity
|
February 13, 1999
A comparative approach to physical and linkage mapping of genes on canine chromosomes using gene-associated simple sequence repeat polymorphisms illustrated by studies of dog chromosome 9
P Werner, M G Raducha, U Prociuk, et al.
Genomics
|
May 15, 1997
Physical and linkage mapping of human chromosome 17 loci to dog chromosomes 9 and 5
P Werner, M G Raducha, U Prociuk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 15, 1992
Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia
P S Henthorn, M Raducha, K N Fedde, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 60) with videos related to
Sort By:
Page
of 6
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1986
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster
P S Henthorn, D L Mager, T H Huisman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Localization of two alkaline phosphatase genes to the proximal region of mouse chromosome 1
E Schurr, P S Henthorn, H Harris, et al.
Journal of the American Animal Hospital Association
|
November 14, 1997
X-linked severe combined immunodeficiency in a family of Cardigan Welsh corgis
R P Pullen, R L Somberg, P J Felsburg, et al.
Cell
|
December 1, 1983
Unexpected relationships between four large deletions in the human beta-globin gene cluster
E F Vanin, P S Henthorn, D Kioussis, et al.
The Journal of Biological Chemistry
|
August 25, 1988
Sequence and characterization of the human intestinal alkaline phosphatase gene
P S Henthorn, M Raducha, T Kadesch, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1996
Aberrant properties of alkaline phosphatase in patient fibroblasts correlate with clinical expressivity in severe forms of hypophosphatasia
K N Fedde, M P Michell, P S Henthorn, et al.
Journal of Veterinary Internal Medicine
|
November 7, 2017
Canine GM2-Gangliosidosis Sandhoff Disease Associated with a 3-Base Pair Deletion in the HEXB Gene
P Wang, P S Henthorn, E Galban, et al.
The Journal of Heredity
|
February 13, 1999
A comparative approach to physical and linkage mapping of genes on canine chromosomes using gene-associated simple sequence repeat polymorphisms illustrated by studies of dog chromosome 9
P Werner, M G Raducha, U Prociuk, et al.
Genomics
|
May 15, 1997
Physical and linkage mapping of human chromosome 17 loci to dog chromosomes 9 and 5
P Werner, M G Raducha, U Prociuk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 15, 1992
Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia
P S Henthorn, M Raducha, K N Fedde, et al.
Page
of 6