Search research articles
Contact Us
Filters
Showing results (341-350 of 347) with videos related to
Page
of 35
Sort By:
You have reached the last page of results.
This site can display upto 347 results.
Genomics
|
December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17
S R Diehl, M Boehnke, R P Erickson, et al.
Science (New York, N.Y.)
|
July 7, 1995
Regulation of human gene therapy
G A Chase, P A DeLeon, K R Dronamraju, et al.
American Journal of Human Genetics
|
January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene
S R Diehl, M Boehnke, R P Erickson, et al.
Molecular Psychiatry
|
July 20, 2005
Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistance
H A Garriock, J J B Allen, P Delgado, et al.
Lymphology
|
November 4, 2021
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation
D J Mustacich, R I Kylat, M J Bernas, et al.
Journal of Medical Genetics
|
November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations
R P Erickson, S L Dagenais, M S Caulder, et al.
Journal of Medical Genetics
|
December 5, 2008
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange
J Yan, F Zhang, E Brundage, et al.
Page
of 35
Search research articles
Search
Showing results (341-350 of 347) with videos related to
Sort By:
Page
of 35
You have reached the last page of results.
This site can display upto 347 results.
Genomics
|
December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17
S R Diehl, M Boehnke, R P Erickson, et al.
Science (New York, N.Y.)
|
July 7, 1995
Regulation of human gene therapy
G A Chase, P A DeLeon, K R Dronamraju, et al.
American Journal of Human Genetics
|
January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene
S R Diehl, M Boehnke, R P Erickson, et al.
Molecular Psychiatry
|
July 20, 2005
Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistance
H A Garriock, J J B Allen, P Delgado, et al.
Lymphology
|
November 4, 2021
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation
D J Mustacich, R I Kylat, M J Bernas, et al.
Journal of Medical Genetics
|
November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations
R P Erickson, S L Dagenais, M S Caulder, et al.
Journal of Medical Genetics
|
December 5, 2008
Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange
J Yan, F Zhang, E Brundage, et al.
Page
of 35