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American Journal of Medical Genetics. Part A
|
June 11, 2021
Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformations
Vanessa Franziska Schmidt, Ilse Wieland, Walter A Wohlgemuth, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2014
Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutations
Luzie Bülow, Christina Lissewski, Rainer Bressel, et al.
European Journal of Medical Genetics
|
January 24, 2017
Novel FREM1 mutations in a patient with MOTA syndrome: Clinical findings, mutation update and review of FREM1-related disorders literature
Oscar F Chacon-Camacho, Martin Zenker, Denny Schanze, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasia
Alireza Baradaran-Heravi, Christian Thiel, Anita Rauch, et al.
Gene Expression Patterns : GEP
|
October 7, 2021
Galloway-Mowat syndrome: New insights from bioinformatics and expression during Xenopus embryogenesis
Ernestine Treimer, Kathrin Niedermayer, Sven Schumann, et al.
Anticancer Research
|
June 4, 2020
Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg
Reinhard E Friedrich, Christian Hagel, Felix K Kohlrusch, et al.
Journal of Inorganic Biochemistry
|
August 3, 2010
Preparation, 99mTc-labeling and biodistribution studies of a PNA oligomer containing a new ligand derivative of 2,2'-dipicolylamine
Gilles Gasser, Katrin Jäger, Martin Zenker, et al.
Cell Cycle (Georgetown, Tex.)
|
August 22, 2006
Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disorders
Christian P Kratz, Suzanne Schubbert, Gideon Bollag, et al.
The Journal of Pediatrics
|
October 16, 2002
Treatment of two patients with Herlitz junctional epidermolysis bullosa with artificial skin bioequivalents
Qiu-Jie Jiang, Jan Izakovic, Martin Zenker, et al.
The American Journal of Gastroenterology
|
August 16, 2008
Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern Germany
Frank Ulrich Weiss, Martin Zenker, Arif Bülent Ekici, et al.
Page
of 34
Search research articles
Search
Showing results (71-80 of 338) with videos related to
Sort By:
Page
of 34
American Journal of Medical Genetics. Part A
|
June 11, 2021
Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformations
Vanessa Franziska Schmidt, Ilse Wieland, Walter A Wohlgemuth, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2014
Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutations
Luzie Bülow, Christina Lissewski, Rainer Bressel, et al.
European Journal of Medical Genetics
|
January 24, 2017
Novel FREM1 mutations in a patient with MOTA syndrome: Clinical findings, mutation update and review of FREM1-related disorders literature
Oscar F Chacon-Camacho, Martin Zenker, Denny Schanze, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasia
Alireza Baradaran-Heravi, Christian Thiel, Anita Rauch, et al.
Gene Expression Patterns : GEP
|
October 7, 2021
Galloway-Mowat syndrome: New insights from bioinformatics and expression during Xenopus embryogenesis
Ernestine Treimer, Kathrin Niedermayer, Sven Schumann, et al.
Anticancer Research
|
June 4, 2020
Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg
Reinhard E Friedrich, Christian Hagel, Felix K Kohlrusch, et al.
Journal of Inorganic Biochemistry
|
August 3, 2010
Preparation, 99mTc-labeling and biodistribution studies of a PNA oligomer containing a new ligand derivative of 2,2'-dipicolylamine
Gilles Gasser, Katrin Jäger, Martin Zenker, et al.
Cell Cycle (Georgetown, Tex.)
|
August 22, 2006
Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disorders
Christian P Kratz, Suzanne Schubbert, Gideon Bollag, et al.
The Journal of Pediatrics
|
October 16, 2002
Treatment of two patients with Herlitz junctional epidermolysis bullosa with artificial skin bioequivalents
Qiu-Jie Jiang, Jan Izakovic, Martin Zenker, et al.
The American Journal of Gastroenterology
|
August 16, 2008
Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern Germany
Frank Ulrich Weiss, Martin Zenker, Arif Bülent Ekici, et al.
Page
of 34