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E Tiller

Showing results (41-50 of 60) with videos related to

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Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
Gene|January 31, 1997
Isolation and characterization of a mammalian homolog of the Drosophila white geneJ M Croop, G E Tiller, J A Fletcher, et al.
Genomics|September 1, 1993
Physical and linkage mapping of the human and murine genes for the alpha 1 chain of type IX collagen (COL9A1)M L Warman, G E Tiller, P A Polumbo, et al.
Genomics|March 24, 1999
Multiple inositol polyphosphate phosphatase: evolution as a distinct group within the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19H Chi, G E Tiller, M J Dasouki, et al.
Pediatrics|October 7, 2004
Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe diseaseTracy E Hunley, Deyanira Corzo, Martha Dudek, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
The New England Journal of Medicine|February 15, 2001
Enzyme-replacement therapy in mucopolysaccharidosis IE D Kakkis, J Muenzer, G E Tiller, et al.
Skeletal Radiology|May 29, 2012
Metaphyseal chondromatosis combined with D-2-hydroxyglutaric aciduria in four patientsHye Jung Choo, Tae-Joon Cho, Junghan Song, et al.
Genomics|November 20, 1995
Molecular cloning of the alpha 3 chain of human type IX collagen: linkage of the gene COL9A3 to chromosome 20q13.3R G Brewton, B M Wood, Z X Ren, et al.
American Journal of Medical Genetics. Part A|June 20, 2012
A newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delayWagner A R Baratela, Michael B Bober, George E Tiller, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Nature Genetics|September 1, 1995
Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick typeG E Tiller, P A Polumbo, M A Weis, et al.
Gene|January 31, 1997
Isolation and characterization of a mammalian homolog of the Drosophila white geneJ M Croop, G E Tiller, J A Fletcher, et al.
Genomics|September 1, 1993
Physical and linkage mapping of the human and murine genes for the alpha 1 chain of type IX collagen (COL9A1)M L Warman, G E Tiller, P A Polumbo, et al.
Genomics|March 24, 1999
Multiple inositol polyphosphate phosphatase: evolution as a distinct group within the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19H Chi, G E Tiller, M J Dasouki, et al.
Pediatrics|October 7, 2004
Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe diseaseTracy E Hunley, Deyanira Corzo, Martha Dudek, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
The New England Journal of Medicine|February 15, 2001
Enzyme-replacement therapy in mucopolysaccharidosis IE D Kakkis, J Muenzer, G E Tiller, et al.
Skeletal Radiology|May 29, 2012
Metaphyseal chondromatosis combined with D-2-hydroxyglutaric aciduria in four patientsHye Jung Choo, Tae-Joon Cho, Junghan Song, et al.
Genomics|November 20, 1995
Molecular cloning of the alpha 3 chain of human type IX collagen: linkage of the gene COL9A3 to chromosome 20q13.3R G Brewton, B M Wood, Z X Ren, et al.
American Journal of Medical Genetics. Part A|June 20, 2012
A newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delayWagner A R Baratela, Michael B Bober, George E Tiller, et al.
Pageof 6