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M Preising

Showing results (1-10 of 11) with videos related to

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Versicherungsmedizin|March 26, 2003
[Framework for qualified inpatient withdrawal treatment of alcoholics in North Rhine-Westphalia]G Reymann, M Preising
Ophthalmic Genetics|January 23, 1999
IRPA scientific newsletter--a new website to integrate data on hereditary retinal disordersM Preising, B Lorenz
The British Journal of Ophthalmology|August 21, 2003
Causes of blindness at the "Wiyata Guna" School for the Blind, IndonesiaR Sitorus, M Preising, B Lorenz
European Journal of Clinical Nutrition|March 31, 2016
Modelling human height and weight: a Bayesian approach towards model comparisonM Preising, A Suchomlinov, J Tutkuviene, et al.
The British Journal of Ophthalmology|August 25, 2001
Deletion in the OA1 gene in a family with congenital X linked nystagmusM Preising, J P Op de Laak, B Lorenz
Journal of Medical Genetics|January 15, 2003
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patientsR Sitorus, S M Ardjo, B Lorenz, et al.
The British Journal of Ophthalmology|July 26, 2003
An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congenital amaurosisS Heegaard, T Rosenberg, M Preising, et al.
Journal of Biomedical Engineering|October 1, 1988
Carrier detection of Duchenne dystrophy by frequency analysis of the electromyogramB M Preising, M L Hull, R G Taylor, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 26, 2001
A novel missense mutation of the CBFA1 gene in a family with cleidocranial dysplasia (CCD) and variable expressivityI Golan, M Preising, H Wagener, et al.
Orthodontics & Craniofacial Research|November 6, 2002
Atypical expression of cleidocranial dysplasia: clinical and molecular-genetic analysisI Golan, U Baumert, H Wagener, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Versicherungsmedizin|March 26, 2003
[Framework for qualified inpatient withdrawal treatment of alcoholics in North Rhine-Westphalia]G Reymann, M Preising
Ophthalmic Genetics|January 23, 1999
IRPA scientific newsletter--a new website to integrate data on hereditary retinal disordersM Preising, B Lorenz
The British Journal of Ophthalmology|August 21, 2003
Causes of blindness at the "Wiyata Guna" School for the Blind, IndonesiaR Sitorus, M Preising, B Lorenz
European Journal of Clinical Nutrition|March 31, 2016
Modelling human height and weight: a Bayesian approach towards model comparisonM Preising, A Suchomlinov, J Tutkuviene, et al.
The British Journal of Ophthalmology|August 25, 2001
Deletion in the OA1 gene in a family with congenital X linked nystagmusM Preising, J P Op de Laak, B Lorenz
Journal of Medical Genetics|January 15, 2003
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patientsR Sitorus, S M Ardjo, B Lorenz, et al.
The British Journal of Ophthalmology|July 26, 2003
An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congenital amaurosisS Heegaard, T Rosenberg, M Preising, et al.
Journal of Biomedical Engineering|October 1, 1988
Carrier detection of Duchenne dystrophy by frequency analysis of the electromyogramB M Preising, M L Hull, R G Taylor, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 26, 2001
A novel missense mutation of the CBFA1 gene in a family with cleidocranial dysplasia (CCD) and variable expressivityI Golan, M Preising, H Wagener, et al.
Orthodontics & Craniofacial Research|November 6, 2002
Atypical expression of cleidocranial dysplasia: clinical and molecular-genetic analysisI Golan, U Baumert, H Wagener, et al.
Pageof 2