Suchergebnisse
UB Katalog
Artikel & mehr
Suchmaske
Suchergebnisse einschränken oder erweitern
Aktive Suchfilter
Weniger Treffer
Gefunden in
- Academic Search Index 12 Treffer
- Complementary Index 12 Treffer
- Science Citation Index Expanded 10 Treffer
- OpenAIRE 9 Treffer
- Gale Academic OneFile 9 Treffer
-
9 weitere Werte:
- Gale OneFile: Health and Medicine 9 Treffer
- Gale In Context: Science 9 Treffer
- Directory of Open Access Journals 6 Treffer
- BASE 3 Treffer
- NARCIS 2 Treffer
- British Library Document Supply Centre Inside Serials & Conference Proceedings 2 Treffer
- Springer Nature Journals 2 Treffer
- eScholarship 1 Treffer
- Gale In Context: Opposing Viewpoints 1 Treffer
Art der Quelle
Schlagwort
- medicine 16 Treffer
- diagnosis 14 Treffer
- research 14 Treffer
- cerebellar atrophy 10 Treffer
- genomics 10 Treffer
-
45 weitere Werte:
- health 10 Treffer
- cerebellar ataxia 9 Treffer
- diagnostic odyssey 9 Treffer
- general medicine 9 Treffer
- genetics (clinical) 9 Treffer
- pharmacology (medical) 9 Treffer
- 03 medical and health sciences 8 Treffer
- itpr1 8 Treffer
- policy 8 Treffer
- undiagnosed 8 Treffer
- 0302 clinical medicine 7 Treffer
- 030217 neurology & neurosurgery 7 Treffer
- humans 7 Treffer
- precision public health 7 Treffer
- retinitis pigmentosa 7 Treffer
- gene identification 6 Treffer
- genetic disorders 6 Treffer
- genetics(clinical) 6 Treffer
- medicine(all) 6 Treffer
- medicine.disease 6 Treffer
- medicine.medical_specialty 6 Treffer
- phenomics 6 Treffer
- public health 6 Treffer
- 0303 health sciences 5 Treffer
- 030304 developmental biology 5 Treffer
- business 5 Treffer
- business.industry 5 Treffer
- genetic aspects 5 Treffer
- lcsh:medicine 5 Treffer
- lcsh:r 5 Treffer
- peroxisomes 5 Treffer
- polyneuropathy 5 Treffer
- sensorineural hearing loss 5 Treffer
- 3. good health 4 Treffer
- care and treatment 4 Treffer
- dna sequencing -- genetic aspects 4 Treffer
- female 4 Treffer
- genetics 4 Treffer
- intellectual disability 4 Treffer
- male 4 Treffer
- medical care 4 Treffer
- medicine.symptom 4 Treffer
- missense mutation 4 Treffer
- mrna export 4 Treffer
- nucleotide sequence 4 Treffer
Verlag
Sprache
Geographischer Bezug
24 Treffer
-
In: Orphanet Journal of Rare Diseases, Jg. 7 (2012), Heft 1, S. 90-98Online academicJournalZugriff:
-
In: Orphanet Journal of Rare Diseases, Jg. 7 (2012), Heft 1, S. 67-73Online academicJournalZugriff:
-
In: Orphanet Journal of Rare Diseases, Jg. 11, Heft 1Online unknownZugriff:
-
In: Orphanet Journal of Rare Diseases, Jg. 7, Heft 1, S. 39-39Online unknownZugriff: