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Cell
|
December 27, 1996
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2
M Vikkula, L M Boon, K L Carraway, et al.
Journal of Medical Genetics
|
April 15, 2006
SMAD4 mutations found in unselected HHT patients
C J Gallione, J A Richards, T G W Letteboer, et al.
American Journal of Human Genetics
|
April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
I K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Human Molecular Genetics
|
June 17, 1999
Allelic and locus heterogeneity in inherited venous malformations
J T Calvert, T J Riney, C D Kontos, et al.
Psychosomatic Medicine
|
April 9, 2001
Central nervous system serotonin function and cardiovascular responses to stress
R B Williams, D A Marchuk, K M Gadde, et al.
Neurogenetics
|
May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
A Ashley-Koch, E R Bonner, P C Gaskell, et al.
Nature Genetics
|
June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
D W Johnson, J N Berg, M A Baldwin, et al.
Genome Research
|
November 1, 1995
Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig
E W Johnson, L M Iyer, S S Rich, et al.
Human Mutation
|
April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles
C J Gallione, D J Klaus, E Y Yeh, et al.
Human Molecular Genetics
|
November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)
T Sahoo, E W Johnson, J W Thomas, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 70) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 70 results.
Cell
|
December 27, 1996
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2
M Vikkula, L M Boon, K L Carraway, et al.
Journal of Medical Genetics
|
April 15, 2006
SMAD4 mutations found in unselected HHT patients
C J Gallione, J A Richards, T G W Letteboer, et al.
American Journal of Human Genetics
|
April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
I K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Human Molecular Genetics
|
June 17, 1999
Allelic and locus heterogeneity in inherited venous malformations
J T Calvert, T J Riney, C D Kontos, et al.
Psychosomatic Medicine
|
April 9, 2001
Central nervous system serotonin function and cardiovascular responses to stress
R B Williams, D A Marchuk, K M Gadde, et al.
Neurogenetics
|
May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
A Ashley-Koch, E R Bonner, P C Gaskell, et al.
Nature Genetics
|
June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
D W Johnson, J N Berg, M A Baldwin, et al.
Genome Research
|
November 1, 1995
Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig
E W Johnson, L M Iyer, S S Rich, et al.
Human Mutation
|
April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles
C J Gallione, D J Klaus, E Y Yeh, et al.
Human Molecular Genetics
|
November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)
T Sahoo, E W Johnson, J W Thomas, et al.
Page
of 7