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Showing results (31-40 of 37) with videos related to

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Genomics|August 1, 1994
Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome geneV Biancalana, E Trivier, C Weber, et al.
Human Genetics|March 1, 1994
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2)P S Rowe, J Goulding, A Read, et al.
Human Genetics|July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic ricketsP S Rowe, J Goulding, A Read, 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 ricketsM J Econs, N E Friedman, P S Rowe, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residuesD Filisetti, G Ostermann, M von Bredow, 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 ricketsF Francis, T M Strom, S Hennig, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Genomics|August 1, 1994
Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome geneV Biancalana, E Trivier, C Weber, et al.
Human Genetics|March 1, 1994
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2)P S Rowe, J Goulding, A Read, et al.
Human Genetics|July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic ricketsP S Rowe, J Goulding, A Read, 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 ricketsM J Econs, N E Friedman, P S Rowe, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residuesD Filisetti, G Ostermann, M von Bredow, 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 ricketsF Francis, T M Strom, S Hennig, et al.
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