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E Schwinger

Showing results (151-160 of 213) with videos related to

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Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probeA Gal, M Beck, A C Sewell, et al.
Investigative Ophthalmology & Visual Science|December 10, 1999
A point mutation (W70A) in the rod PDE-gamma gene desensitizing and delaying murine rod photoreceptorsD J Salchow, P Gouras, K Doi, et al.
Human Reproduction (Oxford, England)|November 26, 1999
Genetics of male subfertility: consequences for the clinical work-upW Küpker, E Schwinger, O Hiort, et al.
Geburtshilfe Und Frauenheilkunde|December 1, 1991
[Diagnosis of fetal virus infections by in situ hybridization]Y Mehraein, H Rehder, H G Draeger, et al.
Human Heredity|January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from IndiaP K Seth, C Meissner, W Kress, et al.
American Journal of Medical Genetics|December 3, 1999
Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophreniaV Arolt, R Lencer, S Purmann, et al.
Genomics|June 1, 1992
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21M B Petersen, O Bartsch, P A Adelsberger, et al.
International Journal of Andrology|September 30, 2000
Comparative study of disomy and diploidy rates in spermatozoa of fertile and infertile men: a donor-adapted protocol for multi-colour fluorescence in situ hybridization (FISH)H Schultz, K Mennicke, H Schlieker, et al.
International Journal of Andrology|January 1, 1997
Molecular cytogenetic diagnostics in spermK Mennicke, P Diercks, H Schlieker, et al.
Pageof 22

Showing results (151-160 of 213) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probeA Gal, M Beck, A C Sewell, et al.
Investigative Ophthalmology & Visual Science|December 10, 1999
A point mutation (W70A) in the rod PDE-gamma gene desensitizing and delaying murine rod photoreceptorsD J Salchow, P Gouras, K Doi, et al.
Human Reproduction (Oxford, England)|November 26, 1999
Genetics of male subfertility: consequences for the clinical work-upW Küpker, E Schwinger, O Hiort, et al.
Geburtshilfe Und Frauenheilkunde|December 1, 1991
[Diagnosis of fetal virus infections by in situ hybridization]Y Mehraein, H Rehder, H G Draeger, et al.
Human Heredity|January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from IndiaP K Seth, C Meissner, W Kress, et al.
American Journal of Medical Genetics|December 3, 1999
Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophreniaV Arolt, R Lencer, S Purmann, et al.
Genomics|June 1, 1992
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21M B Petersen, O Bartsch, P A Adelsberger, et al.
International Journal of Andrology|September 30, 2000
Comparative study of disomy and diploidy rates in spermatozoa of fertile and infertile men: a donor-adapted protocol for multi-colour fluorescence in situ hybridization (FISH)H Schultz, K Mennicke, H Schlieker, et al.
International Journal of Andrology|January 1, 1997
Molecular cytogenetic diagnostics in spermK Mennicke, P Diercks, H Schlieker, et al.
Pageof 22