Search research articles
Contact Us
Filters
Showing results (31-40 of 84) with videos related to
Page
of 9
Sort By:
American Journal of Human Genetics
|
May 1, 1994
Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmenti
S Das, A Metzenberg, G S Pai, et al.
Current Protocols in Chemical Biology
|
March 22, 2014
Label-free cell-based dynamic mass redistribution assays
Hannah J Gitschier, Audrey B Bergeron, David H Randle
Blood
|
September 1, 1988
Mutations of factor VIII cleavage sites in hemophilia A
J Gitschier, S Kogan, B Levinson, et al.
Genomics
|
May 1, 1990
A transcribed gene in an intron of the human factor VIII gene
B Levinson, S Kenwrick, D Lakich, et al.
Human Molecular Genetics
|
June 1, 1992
Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene
S Kenwrick, B Levinson, S Taylor, et al.
Nature Genetics
|
October 1, 1992
Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus
Y Pan, A Metzenberg, S Das, et al.
Nature Genetics
|
November 1, 1993
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A
D Lakich, H H Kazazian, S E Antonarakis, et al.
Nature Genetics
|
January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
C Vulpe, B Levinson, S Whitney, et al.
Genomics
|
August 1, 1992
Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage
C J Faust, B Levinson, J Gitschier, et al.
Nucleic Acids Research
|
May 11, 1991
A new PstI polymorphism between VK21 and St14 in Xq28 (DXS523)
S Kenwrick, P Bridge, D Lillicrap, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 84) with videos related to
Sort By:
Page
of 9
American Journal of Human Genetics
|
May 1, 1994
Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmenti
S Das, A Metzenberg, G S Pai, et al.
Current Protocols in Chemical Biology
|
March 22, 2014
Label-free cell-based dynamic mass redistribution assays
Hannah J Gitschier, Audrey B Bergeron, David H Randle
Blood
|
September 1, 1988
Mutations of factor VIII cleavage sites in hemophilia A
J Gitschier, S Kogan, B Levinson, et al.
Genomics
|
May 1, 1990
A transcribed gene in an intron of the human factor VIII gene
B Levinson, S Kenwrick, D Lakich, et al.
Human Molecular Genetics
|
June 1, 1992
Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene
S Kenwrick, B Levinson, S Taylor, et al.
Nature Genetics
|
October 1, 1992
Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus
Y Pan, A Metzenberg, S Das, et al.
Nature Genetics
|
November 1, 1993
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A
D Lakich, H H Kazazian, S E Antonarakis, et al.
Nature Genetics
|
January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
C Vulpe, B Levinson, S Whitney, et al.
Genomics
|
August 1, 1992
Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage
C J Faust, B Levinson, J Gitschier, et al.
Nucleic Acids Research
|
May 11, 1991
A new PstI polymorphism between VK21 and St14 in Xq28 (DXS523)
S Kenwrick, P Bridge, D Lillicrap, et al.
Page
of 9