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American Journal of Nephrology
|
September 2, 2019
Comparison of Different Selection Strategies for Tolvaptan Eligibility among Autosomal Dominant Polycystic Kidney Disease Patients
Vera C Wulfmeyer, Bernd Auber, Hermann Haller, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Diagnostic genomic sequencing in critically ill children
Bernd Auber, Gunnar Schmidt, Chen Du, et al.
The Journal of Pediatrics
|
June 30, 2009
A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism
Kristina Jülich, Denise Horn, Peter Burfeind, et al.
Frontiers in Pediatrics
|
June 5, 2023
A holistic approach to maximise diagnostic output in trio exome sequencing
Sandra von Hardenberg, Hannah Wallaschek, Chen Du, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion
Georg M Stettner, Moneef Shoukier, Christoph Höger, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2009
Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia
Knut Brockmann, Heiko Backes, Bernd Auber, et al.
Journal of Virology
|
January 15, 2004
Borna disease virus multiplication in mouse organotypic slice cultures is site-specifically inhibited by gamma interferon but not by interleukin-12
Gregor Friedl, Markus Hofer, Bernd Auber, et al.
Stem Cell Research
|
January 31, 2020
Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis
Kathrin Haake, Tim Wüstefeld, Sylvia Merkert, et al.
Frontiers in Pediatrics
|
April 25, 2024
Current genetic diagnostics in inborn errors of immunity
Sandra von Hardenberg, Isabel Klefenz, Doris Steinemann, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2018
KBG syndrome patient due to 16q24.3 microdeletion presenting with a paratesticular rhabdoid tumor: Coincidence or cancer predisposition?
Astrid Behnert, Bernd Auber, Doris Steinemann, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
American Journal of Nephrology
|
September 2, 2019
Comparison of Different Selection Strategies for Tolvaptan Eligibility among Autosomal Dominant Polycystic Kidney Disease Patients
Vera C Wulfmeyer, Bernd Auber, Hermann Haller, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 6, 2024
Diagnostic genomic sequencing in critically ill children
Bernd Auber, Gunnar Schmidt, Chen Du, et al.
The Journal of Pediatrics
|
June 30, 2009
A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism
Kristina Jülich, Denise Horn, Peter Burfeind, et al.
Frontiers in Pediatrics
|
June 5, 2023
A holistic approach to maximise diagnostic output in trio exome sequencing
Sandra von Hardenberg, Hannah Wallaschek, Chen Du, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion
Georg M Stettner, Moneef Shoukier, Christoph Höger, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2009
Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia
Knut Brockmann, Heiko Backes, Bernd Auber, et al.
Journal of Virology
|
January 15, 2004
Borna disease virus multiplication in mouse organotypic slice cultures is site-specifically inhibited by gamma interferon but not by interleukin-12
Gregor Friedl, Markus Hofer, Bernd Auber, et al.
Stem Cell Research
|
January 31, 2020
Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis
Kathrin Haake, Tim Wüstefeld, Sylvia Merkert, et al.
Frontiers in Pediatrics
|
April 25, 2024
Current genetic diagnostics in inborn errors of immunity
Sandra von Hardenberg, Isabel Klefenz, Doris Steinemann, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2018
KBG syndrome patient due to 16q24.3 microdeletion presenting with a paratesticular rhabdoid tumor: Coincidence or cancer predisposition?
Astrid Behnert, Bernd Auber, Doris Steinemann, et al.
Page
of 7