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Nature Genetics
|
May 1, 1994
Human haploinsufficiency--one for sorrow, two for joy
E Fisher, P Scambler
Clinical Genetics
|
August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletion
L M Bird, P Scambler
American Journal of Human Genetics
|
January 1, 1986
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4
M Farrall, P Scambler, P North, et al.
Journal of Medical Genetics
|
September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype
J Goodship, I Cross, P Scambler, et al.
Lancet (London, England)
|
November 28, 1992
Possible role for COMT in psychosis associated with velo-cardio-facial syndrome
I Dunham, J Collins, R Wadey, et al.
Gene
|
April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripes
R Llevadot, X Estivill, P Scambler, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 1, 1996
Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndrome
R Llevadot, P Scambler, X Estivill, et al.
Nucleic Acids Research
|
February 25, 1989
Probe pJ1 [D7S402] detects a MspI RFLP on chromosome 7q31-32
M Ramsay, H Sutherland, R Williamson, et al.
Medical Engineering & Physics
|
August 13, 2010
Mitral valve dynamics in structural and fluid-structure interaction models
K D Lau, V Diaz, P Scambler, et al.
Genomics
|
February 10, 1995
Cloning and mapping of murine Nfe2l1
J McKie, K Johnstone, M G Mattei, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 58) with videos related to
Sort By:
Page
of 6
Nature Genetics
|
May 1, 1994
Human haploinsufficiency--one for sorrow, two for joy
E Fisher, P Scambler
Clinical Genetics
|
August 17, 2000
Cortical dysgenesis in 2 patients with chromosome 22q11 deletion
L M Bird, P Scambler
American Journal of Human Genetics
|
January 1, 1986
The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4
M Farrall, P Scambler, P North, et al.
Journal of Medical Genetics
|
September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype
J Goodship, I Cross, P Scambler, et al.
Lancet (London, England)
|
November 28, 1992
Possible role for COMT in psychosis associated with velo-cardio-facial syndrome
I Dunham, J Collins, R Wadey, et al.
Gene
|
April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripes
R Llevadot, X Estivill, P Scambler, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 1, 1996
Genomic organization of TUPLE1/HIRA: a gene implicated in DiGeorge syndrome
R Llevadot, P Scambler, X Estivill, et al.
Nucleic Acids Research
|
February 25, 1989
Probe pJ1 [D7S402] detects a MspI RFLP on chromosome 7q31-32
M Ramsay, H Sutherland, R Williamson, et al.
Medical Engineering & Physics
|
August 13, 2010
Mitral valve dynamics in structural and fluid-structure interaction models
K D Lau, V Diaz, P Scambler, et al.
Genomics
|
February 10, 1995
Cloning and mapping of murine Nfe2l1
J McKie, K Johnstone, M G Mattei, et al.
Page
of 6