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Showing results (121-130 of 270) with videos related to

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Pharmacogenetics|July 18, 2000
Pharmacological properties of naturally occurring variants of the human norepinephrine transporterF Runkel, M Brüss, M M Nöthen, et al.
Lancet (London, England)|May 27, 1995
Tyrosine hydroxylase gene and manic-depressive illnessM Rietschel, M M Nöthen, W Maier, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1993
The use of microsatellites in zygosity diagnosis of twinsJ Erdmann, M M Nöthen, M Stratmann, et al.
Human Heredity|April 4, 1998
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among EuropeansY Wang, W Friedl, C Lamberti, et al.
Human Genetics|May 1, 1996
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC proteinW Friedl, S Meuschel, R Caspari, et al.
Genetic Epidemiology|January 1, 1988
Alcohol effects on the percentage of beta waves in the electroencephalograms of twinsJ C Christian, T K Li, J A Norton, et al.
Deutsche Medizinische Wochenschrift (1946)|March 4, 2000
[The diagnosis of hereditary colorectal carcinomas]R Caspari, M Jungck, C Lamberti, et al.
European Journal of Pediatrics|February 1, 1991
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophyJ Kappler, R W Watts, E Conzelmann, et al.
Cancer Detection and Prevention|March 29, 2001
Detection of APC and k-ras mutations in the serum of patients with colorectal cancerH Lauschke, R Caspari, W Friedl, et al.
The Journal of Investigative Dermatology|January 14, 1999
A novel germline mutation in the hMLH1 DNA mismatch repair gene in a patient with an isolated cystic sebaceous tumorR Kruse, A Rütten, H R Malayeri, et al.
Pageof 27

Showing results (121-130 of 270) with videos related to

Sort By:
Pageof 27
Pharmacogenetics|July 18, 2000
Pharmacological properties of naturally occurring variants of the human norepinephrine transporterF Runkel, M Brüss, M M Nöthen, et al.
Lancet (London, England)|May 27, 1995
Tyrosine hydroxylase gene and manic-depressive illnessM Rietschel, M M Nöthen, W Maier, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1993
The use of microsatellites in zygosity diagnosis of twinsJ Erdmann, M M Nöthen, M Stratmann, et al.
Human Heredity|April 4, 1998
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among EuropeansY Wang, W Friedl, C Lamberti, et al.
Human Genetics|May 1, 1996
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC proteinW Friedl, S Meuschel, R Caspari, et al.
Genetic Epidemiology|January 1, 1988
Alcohol effects on the percentage of beta waves in the electroencephalograms of twinsJ C Christian, T K Li, J A Norton, et al.
Deutsche Medizinische Wochenschrift (1946)|March 4, 2000
[The diagnosis of hereditary colorectal carcinomas]R Caspari, M Jungck, C Lamberti, et al.
European Journal of Pediatrics|February 1, 1991
Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophyJ Kappler, R W Watts, E Conzelmann, et al.
Cancer Detection and Prevention|March 29, 2001
Detection of APC and k-ras mutations in the serum of patients with colorectal cancerH Lauschke, R Caspari, W Friedl, et al.
The Journal of Investigative Dermatology|January 14, 1999
A novel germline mutation in the hMLH1 DNA mismatch repair gene in a patient with an isolated cystic sebaceous tumorR Kruse, A Rütten, H R Malayeri, et al.
Pageof 27