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American Journal of Medical Genetics
|
May 1, 1986
Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy
G N Wilson, R G Holmes, J Custer, et al.
American Journal of Medical Genetics
|
March 1, 1989
Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy
G N Wilson, J P de Chadarévian, P Kaplan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1974
Cell-free transcription of mammalian chromatin: transcription of globin messenger RNA sequences from bone-marrow chromatin with mammalian RNA polymerase
A W Steggles, G N Wilson, J A Kantor, et al.
American Journal of Medical Genetics
|
January 16, 1995
Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly
A S Kulharya, M Maberry, M K Kukolich, et al.
American Journal of Medical Genetics
|
August 5, 2000
Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group
L D McDaniel, R Prueitt, L C Probst, et al.
The Journal of Reproductive Medicine
|
March 1, 1986
Detection of neural tube defects with alpha-fetoprotein measurement in amniotic fluid. A protocol for managing elevated values
G N Wilson, A Raj, J R Waterson, et al.
American Journal of Human Genetics
|
June 1, 1990
The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history
G P Nowinski, D L Van Dyke, B C Tilley, et al.
Journal of Cellular Physiology
|
April 1, 1975
Activation and inactivation of genes determining hemoglobin types.20s
W F Anderson, J E Barker, N A Elson, et al.
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of 9
Search research articles
Search
Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
American Journal of Medical Genetics
|
May 1, 1986
Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy
G N Wilson, R G Holmes, J Custer, et al.
American Journal of Medical Genetics
|
March 1, 1989
Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy
G N Wilson, J P de Chadarévian, P Kaplan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1974
Cell-free transcription of mammalian chromatin: transcription of globin messenger RNA sequences from bone-marrow chromatin with mammalian RNA polymerase
A W Steggles, G N Wilson, J A Kantor, et al.
American Journal of Medical Genetics
|
January 16, 1995
Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly
A S Kulharya, M Maberry, M K Kukolich, et al.
American Journal of Medical Genetics
|
August 5, 2000
Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group
L D McDaniel, R Prueitt, L C Probst, et al.
The Journal of Reproductive Medicine
|
March 1, 1986
Detection of neural tube defects with alpha-fetoprotein measurement in amniotic fluid. A protocol for managing elevated values
G N Wilson, A Raj, J R Waterson, et al.
American Journal of Human Genetics
|
June 1, 1990
The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history
G P Nowinski, D L Van Dyke, B C Tilley, et al.
Journal of Cellular Physiology
|
April 1, 1975
Activation and inactivation of genes determining hemoglobin types.20s
W F Anderson, J E Barker, N A Elson, et al.
Page
of 9