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M Stuhrmann

Showing results (31-40 of 60) with videos related to

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Human Genetics|November 1, 1995
Direct molecular analysis of the fragile X syndrome in a sample of Egyptian and German patients using non-radioactive PCR and Southern blot followed by chemiluminescent detectionA A el-Aleem, I Böhm, S Temtamy, et al.
Fortschritte Der Neurologie-Psychiatrie|December 5, 2000
[The importance of the endogenous cannabinoid system in various neuropsychiatric disorders]U Schneider, K R Muller-Vahl, M Stuhrmann, et al.
Human Mutation|March 25, 1999
Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. OnlineM Ebhardt, H Schmidt, T Doerk, et al.
Klinische Padiatrie|May 11, 2010
Neonatal Marfan syndrome: unusually large deletion of exons 24-26 of FBN1 associated with poor prognosisC Apitz, S Mackensen-Haen, M Girisch, et al.
British Journal of Haematology|March 22, 2001
Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab familyM Stuhrmann, L Bashawri, M A Ahmed, et al.
Journal of Affective Disorders|April 23, 2022
The interplay of chronic stress and genetic traits discriminates between patients suffering from multisomatoform disorder with pain as the leading symptom and matched controlsM Buhck, J Achenbach, B Wiese, et al.
Clinical Genetics|January 24, 1998
Detection of 100% of the CFTR mutations in 63 CF families from TyrolM Stuhrmann, T Dörk, M Frühwirth, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech familiesM Macek, V Vavrová, I Böhm, et al.
Human Genetics|September 1, 1990
Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German populationA Reis, S Bremer, M Schlösser, et al.
Clinical Genetics|March 11, 1991
The direct early diagnosis of cystic fibrosis by the detection of the delta F508 CFTR gene mutation in a prematurely delivered boyM Macek, M Macek, M Stuhrmann, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Human Genetics|November 1, 1995
Direct molecular analysis of the fragile X syndrome in a sample of Egyptian and German patients using non-radioactive PCR and Southern blot followed by chemiluminescent detectionA A el-Aleem, I Böhm, S Temtamy, et al.
Fortschritte Der Neurologie-Psychiatrie|December 5, 2000
[The importance of the endogenous cannabinoid system in various neuropsychiatric disorders]U Schneider, K R Muller-Vahl, M Stuhrmann, et al.
Human Mutation|March 25, 1999
Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. OnlineM Ebhardt, H Schmidt, T Doerk, et al.
Klinische Padiatrie|May 11, 2010
Neonatal Marfan syndrome: unusually large deletion of exons 24-26 of FBN1 associated with poor prognosisC Apitz, S Mackensen-Haen, M Girisch, et al.
British Journal of Haematology|March 22, 2001
Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab familyM Stuhrmann, L Bashawri, M A Ahmed, et al.
Journal of Affective Disorders|April 23, 2022
The interplay of chronic stress and genetic traits discriminates between patients suffering from multisomatoform disorder with pain as the leading symptom and matched controlsM Buhck, J Achenbach, B Wiese, et al.
Clinical Genetics|January 24, 1998
Detection of 100% of the CFTR mutations in 63 CF families from TyrolM Stuhrmann, T Dörk, M Frühwirth, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech familiesM Macek, V Vavrová, I Böhm, et al.
Human Genetics|September 1, 1990
Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German populationA Reis, S Bremer, M Schlösser, et al.
Clinical Genetics|March 11, 1991
The direct early diagnosis of cystic fibrosis by the detection of the delta F508 CFTR gene mutation in a prematurely delivered boyM Macek, M Macek, M Stuhrmann, et al.
Pageof 6