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Clinical Genetics
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August 2, 2006
Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome
J P Delaunoy, A Dubos, P Marques Pereira, et al.
Clinical Genetics
|
September 13, 2006
Predictive testing for Huntington disease: interpretation and significance of intermediate alleles
A Semaka, S Creighton, S Warby, et al.
Clinical Genetics
|
September 13, 2006
Variability and inequity in testing of somatic tissue for hereditary cancer: a survey of UK clinical practice
C L Gaff, M T Rogers, I M Frayling
Clinical Genetics
|
September 13, 2006
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization
B Drera, D Castiglia, N Zoppi, et al.
Clinical Genetics
|
September 13, 2006
Molecular background of polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome in a Polish population: novel AIRE mutations and an estimate of disease prevalence
B Stolarski, E Pronicka, L Korniszewski, et al.
Clinical Genetics
|
September 7, 2005
Polymorphisms in the apolipoprotein A5 (APOA5) gene and type III hyperlipidemia
D Evans, U Seedorf, F U Beil
Clinical Genetics
|
July 6, 2005
Genetic regulation of stem cell origins in the mouse embryo
A Ralston, J Rossant
Clinical Genetics
|
July 6, 2005
Rare SP-A alleles and the SP-A1-6A(4) allele associate with risk for lung carcinoma
C Seifart, H-M Lin, U Seifart, et al.
Clinical Genetics
|
July 6, 2005
Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia
S-C Lee, J-Y Guo, R Lim, et al.
Clinical Genetics
|
May 1, 1992
GM1-gangliosidosis: tandem duplication within exon 3 of beta-galactosidase gene in an infantile patient
A Oshima, K Yoshida, A Ishizaki, et al.
Page
of 718
Search research articles
Search
Showing results (421-430 of 7,173) with videos related to
Sort By:
Page
of 718
Clinical Genetics
|
August 2, 2006
Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome
J P Delaunoy, A Dubos, P Marques Pereira, et al.
Clinical Genetics
|
September 13, 2006
Predictive testing for Huntington disease: interpretation and significance of intermediate alleles
A Semaka, S Creighton, S Warby, et al.
Clinical Genetics
|
September 13, 2006
Variability and inequity in testing of somatic tissue for hereditary cancer: a survey of UK clinical practice
C L Gaff, M T Rogers, I M Frayling
Clinical Genetics
|
September 13, 2006
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization
B Drera, D Castiglia, N Zoppi, et al.
Clinical Genetics
|
September 13, 2006
Molecular background of polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome in a Polish population: novel AIRE mutations and an estimate of disease prevalence
B Stolarski, E Pronicka, L Korniszewski, et al.
Clinical Genetics
|
September 7, 2005
Polymorphisms in the apolipoprotein A5 (APOA5) gene and type III hyperlipidemia
D Evans, U Seedorf, F U Beil
Clinical Genetics
|
July 6, 2005
Genetic regulation of stem cell origins in the mouse embryo
A Ralston, J Rossant
Clinical Genetics
|
July 6, 2005
Rare SP-A alleles and the SP-A1-6A(4) allele associate with risk for lung carcinoma
C Seifart, H-M Lin, U Seifart, et al.
Clinical Genetics
|
July 6, 2005
Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia
S-C Lee, J-Y Guo, R Lim, et al.
Clinical Genetics
|
May 1, 1992
GM1-gangliosidosis: tandem duplication within exon 3 of beta-galactosidase gene in an infantile patient
A Oshima, K Yoshida, A Ishizaki, et al.
Page
of 718