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Human Genetics|October 1, 1990
A multigene deletion in the immunoglobulin heavy chain region in a highly atopic individualM A Walter, C A Chambers, B Zimmerman, et al.Journal of Neuroimmunology|September 25, 1999
No evidence for association of multiple sclerosis with the complement factors C6 and C7J Chataway, S Sawcer, D Sherman, et al.The Journal of Clinical Endocrinology and Metabolism|March 1, 1993
The role of the sex-determining region Y gene in the etiology of 46,XX malenessP Y Fechner, S M Marcantonio, V Jaswaney, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 17, 2017
Pharmacokinetics of coadministration of levothyroxine sodium and alendronate sodium new effervescent formulationH G Bone, M A Walter, M E Hurley, et al.Infection and Immunity|February 1, 1984
Lack of homology between the iron transport regions of two virulence-linked bacterial plasmidsM A Walter, A Bindereif, J B Neilands, et al.Cell Death & Disease|February 22, 2014
Dysfunction of the stress-responsive FOXC1 transcription factor contributes to the earlier-onset glaucoma observed in Axenfeld-Rieger syndrome patientsY A Ito, I S Goping, F Berry, et al.Nature|October 8, 1992
Evolution of sex determination and the Y chromosome: SRY-related sequences in marsupialsJ W Foster, F E Brennan, G K Hampikian, et al.Nature|July 19, 1990
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motifA H Sinclair, P Berta, M S Palmer, et al.Human Molecular Genetics|March 1, 1996
A radiation hybrid map of the human genomeG Gyapay, K Schmitt, C Fizames, et al.Ophthalmic Genetics|July 27, 1999
Histopathology and molecular basis of iridogoniodysgenesis syndromeW G Pearce, B C Mielke, S C Kulak, et al.Pageof 23