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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.
Neuromuscular Disorders : NMD
|
January 1, 1991
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group
P Raeymaekers, V Timmerman, E Nelis, et al.
Genomics
|
August 1, 1992
Identification of new markers in Xp21 between DXS28 (C7) and DMD
K C Worley, J A Towbin, X M Zhu, et al.
Human Heredity
|
May 1, 1995
Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1
M A Pericak-Vance, D F Barker, J A Bergoffen, et al.
Science (New York, N.Y.)
|
June 8, 1990
Identification of mutations in the COL4A5 collagen gene in Alport syndrome
D F Barker, S L Hostikka, J Zhou, et al.
Human Genetics
|
December 1, 1991
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2
J E Hoogendijk, G W Hensels, I Zorn, et al.
Human Genetics
|
December 1, 1991
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers
D F Barker, P R Fain, D E Goldgar, et al.
Science (New York, N.Y.)
|
April 14, 1989
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas
S J Baker, E R Fearon, J M Nigro, et al.
Cell
|
July 26, 1991
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
September 28, 1998
Expression of mRNA for type IV collagen alpha1, alpha5 and alpha6 chains by cultured dermal fibroblasts from patients with X-linked Alport syndrome
S Sasaki, B Zhou, W W Fan, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
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.
Neuromuscular Disorders : NMD
|
January 1, 1991
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group
P Raeymaekers, V Timmerman, E Nelis, et al.
Genomics
|
August 1, 1992
Identification of new markers in Xp21 between DXS28 (C7) and DMD
K C Worley, J A Towbin, X M Zhu, et al.
Human Heredity
|
May 1, 1995
Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1
M A Pericak-Vance, D F Barker, J A Bergoffen, et al.
Science (New York, N.Y.)
|
June 8, 1990
Identification of mutations in the COL4A5 collagen gene in Alport syndrome
D F Barker, S L Hostikka, J Zhou, et al.
Human Genetics
|
December 1, 1991
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2
J E Hoogendijk, G W Hensels, I Zorn, et al.
Human Genetics
|
December 1, 1991
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers
D F Barker, P R Fain, D E Goldgar, et al.
Science (New York, N.Y.)
|
April 14, 1989
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas
S J Baker, E R Fearon, J M Nigro, et al.
Cell
|
July 26, 1991
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
September 28, 1998
Expression of mRNA for type IV collagen alpha1, alpha5 and alpha6 chains by cultured dermal fibroblasts from patients with X-linked Alport syndrome
S Sasaki, B Zhou, W W Fan, et al.
Page
of 8