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R G Knowlton

Showing results (81-90 of 88) with videos related to

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Nature|November 4, 1985
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7R G Knowlton, O Cohen-Haguenauer, N Van Cong, et al.
American Journal of Human Genetics|November 1, 1989
Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen geneR G Knowlton, E J Weaver, A F Struyk, et al.
Transplantation|March 1, 1987
Use of DNA restriction fragment length polymorphisms to document marrow engraftment and mixed hematopoietic chimerism following bone marrow transplantationP Y Yam, L D Petz, R G Knowlton, et al.
American Journal of Human Genetics|June 1, 1986
Characterization of a spontaneous mutation to a beta-thalassemia alleleH H Kazazian, S H Orkin, C D Boehm, et al.
Genomics|January 20, 1995
D20S16 is a complex interspersed repeated sequence: genetic and physical analysis of the locusD W Bowden, M D Krawchuk, E J Weaver, et al.
Blood|November 1, 1987
Mixed hematopoietic chimerism following bone marrow transplantation for hematologic malignanciesL D Petz, P Yam, R B Wallace, et al.
Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.
American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Nature|November 4, 1985
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7R G Knowlton, O Cohen-Haguenauer, N Van Cong, et al.
American Journal of Human Genetics|November 1, 1989
Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen geneR G Knowlton, E J Weaver, A F Struyk, et al.
Transplantation|March 1, 1987
Use of DNA restriction fragment length polymorphisms to document marrow engraftment and mixed hematopoietic chimerism following bone marrow transplantationP Y Yam, L D Petz, R G Knowlton, et al.
American Journal of Human Genetics|June 1, 1986
Characterization of a spontaneous mutation to a beta-thalassemia alleleH H Kazazian, S H Orkin, C D Boehm, et al.
Genomics|January 20, 1995
D20S16 is a complex interspersed repeated sequence: genetic and physical analysis of the locusD W Bowden, M D Krawchuk, E J Weaver, et al.
Blood|November 1, 1987
Mixed hematopoietic chimerism following bone marrow transplantation for hematologic malignanciesL D Petz, P Yam, R B Wallace, et al.
Nature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.
American Journal of Human Genetics|April 16, 1998
Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrumM D Briggs, G R Mortier, W G Cole, et al.
Pageof 9