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American Journal of Human Genetics
|
July 1, 1993
Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome
M Tassabehji, T Strachan, M Sharland, et al.
Gene
|
October 3, 1998
Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung
M Lako, T Strachan, P Bullen, et al.
Molecular Pharmacology
|
November 26, 2009
Genetic deletion of p90 ribosomal S6 kinase 2 alters patterns of 5-hydroxytryptamine 2A serotonin receptor functional selectivity
Ryan T Strachan, Noah Sciaky, Mark R Cronan, et al.
Human Molecular Genetics
|
May 23, 1998
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain
M Lako, S Lindsay, P Bullen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study
D G Evans, S Mason, S M Huson, et al.
Human Genetics
|
March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families
P J Sinnott, C Livieri, M Sampietro, et al.
Heart Rhythm
|
January 28, 2021
Right ventricular insertion promotes reinitiation of ventricular fibrillation in defibrillation failure
Kenichi Iijima, Hanyu Zhang, Matthew T Strachan, et al.
Human Genetics
|
October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresis
D K Lord, I Dunham, R D Campbell, et al.
Journal of Medical Genetics
|
June 1, 1995
Diagnostic issues in a family with late onset type 2 neurofibromatosis
D G Evans, D Bourn, A Wallace, et al.
The EMBO Journal
|
May 1, 1989
Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes
S Collier, P J Sinnott, P A Dyer, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 138) with videos related to
Sort By:
Page
of 14
American Journal of Human Genetics
|
July 1, 1993
Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome
M Tassabehji, T Strachan, M Sharland, et al.
Gene
|
October 3, 1998
Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung
M Lako, T Strachan, P Bullen, et al.
Molecular Pharmacology
|
November 26, 2009
Genetic deletion of p90 ribosomal S6 kinase 2 alters patterns of 5-hydroxytryptamine 2A serotonin receptor functional selectivity
Ryan T Strachan, Noah Sciaky, Mark R Cronan, et al.
Human Molecular Genetics
|
May 23, 1998
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain
M Lako, S Lindsay, P Bullen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study
D G Evans, S Mason, S M Huson, et al.
Human Genetics
|
March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families
P J Sinnott, C Livieri, M Sampietro, et al.
Heart Rhythm
|
January 28, 2021
Right ventricular insertion promotes reinitiation of ventricular fibrillation in defibrillation failure
Kenichi Iijima, Hanyu Zhang, Matthew T Strachan, et al.
Human Genetics
|
October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresis
D K Lord, I Dunham, R D Campbell, et al.
Journal of Medical Genetics
|
June 1, 1995
Diagnostic issues in a family with late onset type 2 neurofibromatosis
D G Evans, D Bourn, A Wallace, et al.
The EMBO Journal
|
May 1, 1989
Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes
S Collier, P J Sinnott, P A Dyer, et al.
Page
of 14