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Connective Tissue Research
|
August 27, 2014
Abnormal osteopontin and matrix extracellular phosphoglycoprotein localization, and odontoblast differentiation, in X-linked hypophosphatemic teeth
B Salmon, C Bardet, B R Coyac, et al.
Human Genetics
|
July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic rickets
P S Rowe, J Goulding, A Read, et al.
Genomics
|
May 1, 1994
A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate region
F Francis, P S Rowe, M J Econs, et al.
Journal of Dental Research
|
September 8, 2017
Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures
B R Coyac, B Hoac, P Chafey, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus
M J Econs, P S Rowe, F Francis, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 1998
A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets
M J Econs, N E Friedman, P S Rowe, et al.
Human Genetics
|
March 1, 1996
The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)
P S Rowe, J N Goulding, F Francis, et al.
Genome Research
|
June 1, 1997
Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets
F Francis, T M Strom, S Hennig, et al.
Human Molecular Genetics
|
April 1, 1997
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP)
P S Rowe, C L Oudet, F Francis, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Connective Tissue Research
|
August 27, 2014
Abnormal osteopontin and matrix extracellular phosphoglycoprotein localization, and odontoblast differentiation, in X-linked hypophosphatemic teeth
B Salmon, C Bardet, B R Coyac, et al.
Human Genetics
|
July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic rickets
P S Rowe, J Goulding, A Read, et al.
Genomics
|
May 1, 1994
A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate region
F Francis, P S Rowe, M J Econs, et al.
Journal of Dental Research
|
September 8, 2017
Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures
B R Coyac, B Hoac, P Chafey, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus
M J Econs, P S Rowe, F Francis, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 1998
A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets
M J Econs, N E Friedman, P S Rowe, et al.
Human Genetics
|
March 1, 1996
The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)
P S Rowe, J N Goulding, F Francis, et al.
Genome Research
|
June 1, 1997
Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets
F Francis, T M Strom, S Hennig, et al.
Human Molecular Genetics
|
April 1, 1997
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP)
P S Rowe, C L Oudet, F Francis, et al.
Page
of 3