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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
September 11, 2024
Verleihung der GfH-Ehrenmedaille 2024 an Dr. rer. nat. Holger Prokisch
André Reis
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
André Reis
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
July 21, 2025
Awarding of the GfH Medal of Honor 2025 to Prof. Dr. med. Stefan Mundlos: Laudatio by Prof. Dr. med. André Reis, Institute of Human Genetics, Universitätsklinikum Erlangen, on the occasion of the 35. GfH Conference on 02.04.2025 in Innsbruck
André Reis
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
December 4, 2024
Nachruf John M. Opitz, geboren in Hamburg am 15.08.1935, verstorben 31. Oktober 2023 in Salt Lake City, Utah, U. S. A
Anita Rauch, André Reis
Deutsches Arzteblatt International
|
December 5, 2024
The Genetics of Intelligence
André Reis, Frank M Spinath
European Journal of Medical Genetics
|
October 21, 2006
Mild variable Noonan syndrome in a family with a novel PTPN11 mutation
Martin Zenker, Egbert Voss, André Reis
Prenatal Diagnosis
|
February 2, 2006
Prenatal findings in four consecutive pregnancies with fetal Pierson syndrome, a newly defined congenital nephrosis syndrome
Karlheinz Mark, André Reis, Martin Zenker
Archives of Dermatological Research
|
August 23, 2002
Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation
Wolfgang Küster, André Reis, Hans Christian Hennies
American Journal of Medical Genetics. Part A
|
August 13, 2005
Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years ago
Martin Zenker, Michel Pierson, Philippe Jonveaux, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2005
Novel autosomal recessive progressive hyperpigmentation syndrome
Ulrike Hüffmeier, Ingrid Hausser, André Reis, et al.
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Search research articles
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Showing results (1-10 of 276) with videos related to
Sort By:
Page
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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
September 11, 2024
Verleihung der GfH-Ehrenmedaille 2024 an Dr. rer. nat. Holger Prokisch
André Reis
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
André Reis
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
July 21, 2025
Awarding of the GfH Medal of Honor 2025 to Prof. Dr. med. Stefan Mundlos: Laudatio by Prof. Dr. med. André Reis, Institute of Human Genetics, Universitätsklinikum Erlangen, on the occasion of the 35. GfH Conference on 02.04.2025 in Innsbruck
André Reis
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
December 4, 2024
Nachruf John M. Opitz, geboren in Hamburg am 15.08.1935, verstorben 31. Oktober 2023 in Salt Lake City, Utah, U. S. A
Anita Rauch, André Reis
Deutsches Arzteblatt International
|
December 5, 2024
The Genetics of Intelligence
André Reis, Frank M Spinath
European Journal of Medical Genetics
|
October 21, 2006
Mild variable Noonan syndrome in a family with a novel PTPN11 mutation
Martin Zenker, Egbert Voss, André Reis
Prenatal Diagnosis
|
February 2, 2006
Prenatal findings in four consecutive pregnancies with fetal Pierson syndrome, a newly defined congenital nephrosis syndrome
Karlheinz Mark, André Reis, Martin Zenker
Archives of Dermatological Research
|
August 23, 2002
Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation
Wolfgang Küster, André Reis, Hans Christian Hennies
American Journal of Medical Genetics. Part A
|
August 13, 2005
Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years ago
Martin Zenker, Michel Pierson, Philippe Jonveaux, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2005
Novel autosomal recessive progressive hyperpigmentation syndrome
Ulrike Hüffmeier, Ingrid Hausser, André Reis, et al.
Page
of 28