Works matching IS 09365931 AND DT 2020
Results: 38
Frontmatter.
- Published in:
- Medizinische Genetik, 2020, p. I, doi. 10.1515/medgen-2020-frontmatter1
- Publication type:
- Article
On the differential diagnosis of neuropathy in neurogenetic disorders.
- Published in:
- Medizinische Genetik, 2020, p. 243, doi. 10.1515/medgen-2020-2040
- By:
- Publication type:
- Article
Peripheral Neuropathies.
- Published in:
- Medizinische Genetik, 2020, p. 193, doi. 10.1515/medgen-2020-2028
- By:
- Publication type:
- Article
Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020.
- Published in:
- Medizinische Genetik, 2020, p. 207, doi. 10.1515/medgen-2020-2038
- By:
- Publication type:
- Article
Advancing Charcot-Marie-Tooth disease diagnostics, through the UK 100,000 Genomes Project.
- Published in:
- Medizinische Genetik, 2020, p. 227, doi. 10.1515/medgen-2020-2037
- By:
- Publication type:
- Article
Personalia.
- Published in:
- Medizinische Genetik, 2020, p. 281, doi. 10.1515/medgen-2020-2036
- Publication type:
- Article
Aktuelle Nachrichten.
- Published in:
- Medizinische Genetik, 2020, p. 287, doi. 10.1515/medgen-2020-2035
- Publication type:
- Article
Peripheral sensory neuropathies – pain loss vs. pain gain.
- Published in:
- Medizinische Genetik, 2020, p. 233, doi. 10.1515/medgen-2020-2039
- By:
- Publication type:
- Article
Advancing Charcot-Marie-Tooth disease diagnostics, through the UK 100,000 Genomes Project.
- Published in:
- Medizinische Genetik, 2020, p. 227, doi. 10.1515/medgen-2020-2037
- By:
- Publication type:
- Article
Personalia.
- Published in:
- Medizinische Genetik, 2020, p. 281, doi. 10.1515/medgen-2020-2036
- Publication type:
- Article
Aktuelle Nachrichten.
- Published in:
- Medizinische Genetik, 2020, p. 287, doi. 10.1515/medgen-2020-2035
- Publication type:
- Article
Spinal muscular atrophy (5qSMA): best practice of diagnostics, newborn screening and therapy.
- Published in:
- Medizinische Genetik, 2020, p. 263, doi. 10.1515/medgen-2020-2033
- By:
- Publication type:
- Article
BVDH-Verbandsmitteilungen.
- Published in:
- Medizinische Genetik, 2020, p. 283, doi. 10.1515/medgen-2020-2034
- Publication type:
- Article
BVDH-Verbandsmitteilungen.
- Published in:
- Medizinische Genetik, 2020, p. 283, doi. 10.1515/medgen-2020-2034
- Publication type:
- Article
Der Weg in die Einheit: Das Fach Humangenetik 1990–1991. Ein Erfahrungsbericht.
- Published in:
- Medizinische Genetik, 2020, p. 275, doi. 10.1515/medgen-2020-2032
- By:
- Publication type:
- Article
Charcot-Marie-Tooth neuropathy and pregnancy: general and specific issues.
- Published in:
- Medizinische Genetik, 2020, p. 221, doi. 10.1515/medgen-2020-2031
- By:
- Publication type:
- Article
The CMT1A duplication: A historical perspective viewed from two sides of an ocean.
- Published in:
- Medizinische Genetik, 2020, p. 195, doi. 10.1515/medgen-2020-2030
- By:
- Publication type:
- Article
Spinal muscular atrophy (5qSMA): best practice of diagnostics, newborn screening and therapy.
- Published in:
- Medizinische Genetik, 2020, p. 263, doi. 10.1515/medgen-2020-2033
- By:
- Publication type:
- Article
Frontmatter.
- Published in:
- Medizinische Genetik, 2020, p. I, doi. 10.1515/medgen-2020-frontmatter1
- Publication type:
- Article
On the differential diagnosis of neuropathy in neurogenetic disorders.
- Published in:
- Medizinische Genetik, 2020, p. 243, doi. 10.1515/medgen-2020-2040
- By:
- Publication type:
- Article
Peripheral sensory neuropathies – pain loss vs. pain gain.
- Published in:
- Medizinische Genetik, 2020, p. 233, doi. 10.1515/medgen-2020-2039
- By:
- Publication type:
- Article
Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020.
- Published in:
- Medizinische Genetik, 2020, p. 207, doi. 10.1515/medgen-2020-2038
- By:
- Publication type:
- Article
Der Weg in die Einheit: Das Fach Humangenetik 1990–1991. Ein Erfahrungsbericht.
- Published in:
- Medizinische Genetik, 2020, p. 275, doi. 10.1515/medgen-2020-2032
- By:
- Publication type:
- Article
Charcot-Marie-Tooth neuropathy and pregnancy: general and specific issues.
- Published in:
- Medizinische Genetik, 2020, p. 221, doi. 10.1515/medgen-2020-2031
- By:
- Publication type:
- Article
Peripheral Neuropathies.
- Published in:
- Medizinische Genetik, 2020, p. 193, doi. 10.1515/medgen-2020-2028
- By:
- Publication type:
- Article
The CMT1A duplication: A historical perspective viewed from two sides of an ocean.
- Published in:
- Medizinische Genetik, 2020, p. 195, doi. 10.1515/medgen-2020-2030
- By:
- Publication type:
- Article
Frontmatter.
- Published in:
- Medizinische Genetik, 2020, p. I, doi. 10.1515/medgen-2020-frontmatter1
- Publication type:
- Article
Aktuelle Nachrichten.
- Published in:
- Medizinische Genetik, 2020, p. 185, doi. 10.1515/medgen-2020-2029
- By:
- Publication type:
- Article
Combating the SARS-CoV-2 pandemic: How can the field of Human Genetics contribute?
- Published in:
- Medizinische Genetik, 2020, p. 163, doi. 10.1515/medgen-2020-2027
- By:
- Publication type:
- Article
Psychiatrische Versorgung – mutiert und pervertiert: Von einer modernen Psychiatrie zur Tötungsanstalt im Dritten Reich: Pirna-Sonnenstein: Exkursionsbericht des Vereins Psychosoziale Aspekte der Humangenetik e. V. (VPAH).
- Published in:
- Medizinische Genetik, 2020, p. 181, doi. 10.1515/medgen-2020-2025
- By:
- Publication type:
- Article
GfH-Promotionspreise 2020.
- Published in:
- Medizinische Genetik, 2020, p. 177, doi. 10.1515/medgen-2020-2026
- By:
- Publication type:
- Article
Usher syndrome: diagnostic approach, differential diagnoses and proposal of an updated function-based genetic classification.
- Published in:
- Medizinische Genetik, 2020, p. 131, doi. 10.1515/medgen-2020-2023
- By:
- Publication type:
- Article
Non-syndromic hearing loss: clinical and diagnostic challenges.
- Published in:
- Medizinische Genetik, 2020, p. 117, doi. 10.1515/medgen-2020-2022
- By:
- Publication type:
- Article
Gene therapy as a possible option to treat hereditary hearing loss.
- Published in:
- Medizinische Genetik, 2020, p. 149, doi. 10.1515/medgen-2020-2021
- By:
- Publication type:
- Article
Clinical and molecular genetics of Meniere disease.
- Published in:
- Medizinische Genetik, 2020, p. 141, doi. 10.1515/medgen-2020-2019
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- Publication type:
- Article
Leitlinien für die molekulare und zytogenetische Diagnostik bei Prader-Willi-Syndrom und Angelman-Syndrom.
- Published in:
- Medizinische Genetik, 2020, p. 169, doi. 10.1515/medgen-2020-2020
- By:
- Publication type:
- Article
Expert interpretation of genes and variants in hereditary hearing loss.
- Published in:
- Medizinische Genetik, 2020, p. 109, doi. 10.1515/medgen-2020-2018
- By:
- Publication type:
- Article
Hereditary auditory disorders.
- Published in:
- Medizinische Genetik, 2020, p. 107, doi. 10.1515/medgen-2020-2017
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- Publication type:
- Article