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Human Genetics
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April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization
A Clarke, M Sarfarazi, N S Thomas, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 31, 2014
Selective adaptation to "oddball" sounds by the human auditory system
Andrew J R Simpson, Nicol S Harper, Joshua D Reiss, et al.
Gene
|
November 21, 1996
RS cyclophilins: identification of an NK-TR1-related cyclophilin
F P Nestel, K Colwill, S Harper, et al.
Journal of Medical Genetics
|
December 1, 1982
A clinical and genetic study of Hunter's syndrome. 1. Heterogeneity
I D Young, P S Harper, I M Archer, et al.
Lancet (London, England)
|
September 9, 1989
Problems in genetic prediction for Huntington's disease
M J Morris, A Tyler, L Lazarou, et al.
Journal of Medical Genetics
|
December 1, 1989
Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers
A M Norman, J L Floyd, A L Meredith, et al.
Journal of Medical Genetics
|
August 1, 1989
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of Wales
L A Tyfield, A L Meredith, M J Osborn, et al.
Archives of Disease in Childhood
|
July 1, 1979
Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases
J R Sibert, P S Harper, R J Thompson, et al.
The Science of the Total Environment
|
February 8, 2006
Turbidity dynamics during spring storm events in an urban headwater river system: the Upper Tame, West Midlands, UK
D M Lawler, G E Petts, I D L Foster, et al.
Journal of Medical Genetics
|
April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severity
A M Norman, N S Thomas, H M Kingston, et al.
Page
of 123
Search research articles
Search
Showing results (401-410 of 1,225) with videos related to
Sort By:
Page
of 123
Human Genetics
|
April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization
A Clarke, M Sarfarazi, N S Thomas, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 31, 2014
Selective adaptation to "oddball" sounds by the human auditory system
Andrew J R Simpson, Nicol S Harper, Joshua D Reiss, et al.
Gene
|
November 21, 1996
RS cyclophilins: identification of an NK-TR1-related cyclophilin
F P Nestel, K Colwill, S Harper, et al.
Journal of Medical Genetics
|
December 1, 1982
A clinical and genetic study of Hunter's syndrome. 1. Heterogeneity
I D Young, P S Harper, I M Archer, et al.
Lancet (London, England)
|
September 9, 1989
Problems in genetic prediction for Huntington's disease
M J Morris, A Tyler, L Lazarou, et al.
Journal of Medical Genetics
|
December 1, 1989
Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers
A M Norman, J L Floyd, A L Meredith, et al.
Journal of Medical Genetics
|
August 1, 1989
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of Wales
L A Tyfield, A L Meredith, M J Osborn, et al.
Archives of Disease in Childhood
|
July 1, 1979
Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases
J R Sibert, P S Harper, R J Thompson, et al.
The Science of the Total Environment
|
February 8, 2006
Turbidity dynamics during spring storm events in an urban headwater river system: the Upper Tame, West Midlands, UK
D M Lawler, G E Petts, I D L Foster, et al.
Journal of Medical Genetics
|
April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severity
A M Norman, N S Thomas, H M Kingston, et al.
Page
of 123