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Matrix Biology : Journal of the International Society for Matrix Biology
|
July 27, 2001
Calreticulin, PDI, Grp94 and BiP chaperone proteins are associated with retained COMP in pseudoachondroplasia chondrocytes
J T Hecht, E Hayes, M Snuggs, et al.
Genomics
|
December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19
J T Hecht, C A Francomano, M D Briggs, et al.
American Journal of Human Genetics
|
September 1, 1996
Nonsyndromic cleft lip with or without cleft palate: erratum
C Amos, J Stein, J B Mulliken, et al.
Nature Genetics
|
September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
M L Warman, M Abbott, S S Apte, et al.
American Journal of Human Genetics
|
April 1, 1992
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes
G A Greenhaw, A Hebert, M E Duke-Woodside, et al.
American Journal of Human Genetics
|
August 1, 1995
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families
J Stein, J B Mulliken, S Stal, et al.
Nature Genetics
|
July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
G A Bellus, I McIntosh, E A Smith, et al.
American Journal of Human Genetics
|
January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasia
J E Finkelstein, K Doege, Y Yamada, et al.
American Journal of Human Genetics
|
November 1, 1994
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate
H Feng, R Sassani, S P Bartlett, et al.
American Journal of Human Genetics
|
February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3
G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 104) with videos related to
Sort By:
Page
of 11
Matrix Biology : Journal of the International Society for Matrix Biology
|
July 27, 2001
Calreticulin, PDI, Grp94 and BiP chaperone proteins are associated with retained COMP in pseudoachondroplasia chondrocytes
J T Hecht, E Hayes, M Snuggs, et al.
Genomics
|
December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19
J T Hecht, C A Francomano, M D Briggs, et al.
American Journal of Human Genetics
|
September 1, 1996
Nonsyndromic cleft lip with or without cleft palate: erratum
C Amos, J Stein, J B Mulliken, et al.
Nature Genetics
|
September 1, 1993
A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
M L Warman, M Abbott, S S Apte, et al.
American Journal of Human Genetics
|
April 1, 1992
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes
G A Greenhaw, A Hebert, M E Duke-Woodside, et al.
American Journal of Human Genetics
|
August 1, 1995
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families
J Stein, J B Mulliken, S Stal, et al.
Nature Genetics
|
July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
G A Bellus, I McIntosh, E A Smith, et al.
American Journal of Human Genetics
|
January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasia
J E Finkelstein, K Doege, Y Yamada, et al.
American Journal of Human Genetics
|
November 1, 1994
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palate
H Feng, R Sassani, S P Bartlett, et al.
American Journal of Human Genetics
|
February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3
G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.
Page
of 11