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S Hofferbert

Showing results (1-10 of 8) with videos related to

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Human Molecular Genetics|January 1, 1997
Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection methodS Hofferbert, N C Schanen, F Chehab, et al.
Neuropediatrics|June 1, 1997
Is Rett syndrome caused by a triplet repeat expansion?S Hofferbert, N C Schanen, S S Budden, et al.
Blood|May 1, 1991
Point mutations in the L-type pyruvate kinase gene of two children with hemolytic anemia caused by pyruvate kinase deficiencyB Neubauer, M Lakomek, H Winkler, et al.
Human Genetics|June 1, 1996
A novel 5'-upstream mutation in the factor XII gene is associated with a TaqI restriction site in an Alu repeat in factor XII-deficient patientsS Hofferbert, J Müller, H Köstering, et al.
Molecular Reproduction and Development|January 1, 1996
Sequence analysis of the conserved protamine gene cluster shows that it contains a fourth expressed geneG Schlüter, A Celik, R Obata, et al.
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Simultaneous interdisciplinary counseling in German breast/ovarian cancer families: first experiences with patient perceptions, surveillance behavior and acceptance of genetic testingS Hofferbert, U Worringen, J Backe, et al.
Gynecologic Oncology|March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patientsJ Backe, S Hofferbert, B Skawran, et al.
Blood|November 14, 1997
Mutations in the human factor XII geneM Schloesser, S Zeerleder, G Lutze, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|January 1, 1997
Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection methodS Hofferbert, N C Schanen, F Chehab, et al.
Neuropediatrics|June 1, 1997
Is Rett syndrome caused by a triplet repeat expansion?S Hofferbert, N C Schanen, S S Budden, et al.
Blood|May 1, 1991
Point mutations in the L-type pyruvate kinase gene of two children with hemolytic anemia caused by pyruvate kinase deficiencyB Neubauer, M Lakomek, H Winkler, et al.
Human Genetics|June 1, 1996
A novel 5'-upstream mutation in the factor XII gene is associated with a TaqI restriction site in an Alu repeat in factor XII-deficient patientsS Hofferbert, J Müller, H Köstering, et al.
Molecular Reproduction and Development|January 1, 1996
Sequence analysis of the conserved protamine gene cluster shows that it contains a fourth expressed geneG Schlüter, A Celik, R Obata, et al.
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
Simultaneous interdisciplinary counseling in German breast/ovarian cancer families: first experiences with patient perceptions, surveillance behavior and acceptance of genetic testingS Hofferbert, U Worringen, J Backe, et al.
Gynecologic Oncology|March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patientsJ Backe, S Hofferbert, B Skawran, et al.
Blood|November 14, 1997
Mutations in the human factor XII geneM Schloesser, S Zeerleder, G Lutze, et al.
Pageof 1