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American Journal of Human Genetics
|
June 1, 1986
Genetic heterogeneity among kindreds with Alport syndrome
S J Hasstedt, C L Atkin, A C San Juan
American Journal of Medical Genetics
|
February 27, 2001
Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP
D F Barker, J C Denison, C L Atkin, et al.
Pathology, Research and Practice
|
January 1, 1980
Early pathologic features of hereditary nephritis: a clinicopathologic correlation
W M O'Neill, R P Mennemeyer, H A Bloomer, et al.
Human Genetics
|
May 1, 1997
Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q
D F Barker, J C Denison, C L Atkin, et al.
Pediatric Research
|
July 1, 1977
Menkes' Kinky hair syndrome: studies of copper metabolism and long term copper therapy
D M Williams, C L Atkin, D B Frens, et al.
Kidney International
|
October 1, 1989
Identification of variant Alport phenotypes using an Alport-specific antibody probe
C E Kashtan, C L Atkin, M C Gregory, et al.
Blood
|
May 1, 1981
Hereditary myeloperoxidase deficiency
M Kitahara, H J Eyre, Y Simonian, et al.
Infection and Immunity
|
October 8, 1997
Allelic polymorphisms at the H-2A and HLA-DQ loci influence the response of murine lymphocytes to the Mycoplasma arthritidis superantigen MAM
B C Cole, A D Sawitzke, E A Ahmed, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
September 1, 1986
Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. V. A small basic protein from culture supernatants is a potent T cell mitogen
C L Atkin, B C Cole, G J Sullivan, et al.
Genomics
|
January 1, 1991
Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome
J Zhou, D F Barker, S L Hostikka, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
American Journal of Human Genetics
|
June 1, 1986
Genetic heterogeneity among kindreds with Alport syndrome
S J Hasstedt, C L Atkin, A C San Juan
American Journal of Medical Genetics
|
February 27, 2001
Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP
D F Barker, J C Denison, C L Atkin, et al.
Pathology, Research and Practice
|
January 1, 1980
Early pathologic features of hereditary nephritis: a clinicopathologic correlation
W M O'Neill, R P Mennemeyer, H A Bloomer, et al.
Human Genetics
|
May 1, 1997
Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q
D F Barker, J C Denison, C L Atkin, et al.
Pediatric Research
|
July 1, 1977
Menkes' Kinky hair syndrome: studies of copper metabolism and long term copper therapy
D M Williams, C L Atkin, D B Frens, et al.
Kidney International
|
October 1, 1989
Identification of variant Alport phenotypes using an Alport-specific antibody probe
C E Kashtan, C L Atkin, M C Gregory, et al.
Blood
|
May 1, 1981
Hereditary myeloperoxidase deficiency
M Kitahara, H J Eyre, Y Simonian, et al.
Infection and Immunity
|
October 8, 1997
Allelic polymorphisms at the H-2A and HLA-DQ loci influence the response of murine lymphocytes to the Mycoplasma arthritidis superantigen MAM
B C Cole, A D Sawitzke, E A Ahmed, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
September 1, 1986
Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. V. A small basic protein from culture supernatants is a potent T cell mitogen
C L Atkin, B C Cole, G J Sullivan, et al.
Genomics
|
January 1, 1991
Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome
J Zhou, D F Barker, S L Hostikka, et al.
Page
of 3