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Journal of Vascular and Interventional Radiology : JVIR
|
April 2, 1999
Massive hemorrhage complicating percutaneous endoscopic gastrostomy: treatment by means of transcatheter embolization of the right and left gastroepiploic arteries
M B Lewis, J H Lewis, H Marshall, et al.
Neurology
|
February 26, 2000
Delayed myelopathic presentation of the acquired hepatocerebral degeneration syndrome
M B Lewis, G MacQuillan, J M Bamford, et al.
The Cleft Palate Journal
|
January 1, 1981
The prevalence of congenital heart disease among the population of a metropolitan cleft lip and palate clinic
N Geis, B Seto, L Bartoshesky, et al.
American Journal of Medical Genetics
|
August 1, 1991
Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36
A G Hatziioannou, C M Krauss, M B Lewis, et al.
Nucleic Acids Research
|
July 25, 1990
Detection of point mutations in type I collagen by RNase digestion of RNA/RNA hybrids
D K Grange, G S Gottesman, M B Lewis, et al.
Cancer
|
May 1, 1973
Extra-axial spread of medulloblastoma
M B Lewis, L B Nunes, D E Powell, et al.
Human Mutation
|
January 1, 1993
A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV proband
J D Filie, B M Orrison, Q Wang, et al.
Neuroendocrinology
|
January 1, 1986
Differential production of SRIF 14 and 28 by fetal rat hypothalamic cells enriched by velocity sedimentation
M D Lewis, S M Foord, M B Lewis, et al.
The Journal of Biological Chemistry
|
February 5, 1993
Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology
J C Marini, M B Lewis, Q Wang, et al.
The Journal of Biological Chemistry
|
July 15, 1989
Osteogenesis imperfecta type IV. Detection of a point mutation in one alpha 1(I) collagen allele (COL1A1) by RNA/RNA hybrid analysis
J C Marini, D K Grange, G S Gottesman, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Journal of Vascular and Interventional Radiology : JVIR
|
April 2, 1999
Massive hemorrhage complicating percutaneous endoscopic gastrostomy: treatment by means of transcatheter embolization of the right and left gastroepiploic arteries
M B Lewis, J H Lewis, H Marshall, et al.
Neurology
|
February 26, 2000
Delayed myelopathic presentation of the acquired hepatocerebral degeneration syndrome
M B Lewis, G MacQuillan, J M Bamford, et al.
The Cleft Palate Journal
|
January 1, 1981
The prevalence of congenital heart disease among the population of a metropolitan cleft lip and palate clinic
N Geis, B Seto, L Bartoshesky, et al.
American Journal of Medical Genetics
|
August 1, 1991
Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36
A G Hatziioannou, C M Krauss, M B Lewis, et al.
Nucleic Acids Research
|
July 25, 1990
Detection of point mutations in type I collagen by RNase digestion of RNA/RNA hybrids
D K Grange, G S Gottesman, M B Lewis, et al.
Cancer
|
May 1, 1973
Extra-axial spread of medulloblastoma
M B Lewis, L B Nunes, D E Powell, et al.
Human Mutation
|
January 1, 1993
A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV proband
J D Filie, B M Orrison, Q Wang, et al.
Neuroendocrinology
|
January 1, 1986
Differential production of SRIF 14 and 28 by fetal rat hypothalamic cells enriched by velocity sedimentation
M D Lewis, S M Foord, M B Lewis, et al.
The Journal of Biological Chemistry
|
February 5, 1993
Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology
J C Marini, M B Lewis, Q Wang, et al.
The Journal of Biological Chemistry
|
July 15, 1989
Osteogenesis imperfecta type IV. Detection of a point mutation in one alpha 1(I) collagen allele (COL1A1) by RNA/RNA hybrid analysis
J C Marini, D K Grange, G S Gottesman, et al.
Page
of 6