Suchergebnisse
UB Katalog
Artikel & mehr
Suchmaske
Suchergebnisse einschränken oder erweitern
Aktive Suchfilter
Weniger Treffer
Gefunden in
Schlagwort
- genetic linkage 3 Treffer
- genetics (clinical) 3 Treffer
- dna mutational analysis 2 Treffer
- education 2 Treffer
- education.field_of_study 2 Treffer
-
45 weitere Werte:
- exome 2 Treffer
- exome sequencing 2 Treffer
- extracellular matrix proteins 2 Treffer
- gene 2 Treffer
- genetic heterogeneity 2 Treffer
- lebanon 2 Treffer
- male 2 Treffer
- medicine.disease_cause 2 Treffer
- molecular biology 2 Treffer
- mutation 2 Treffer
- myosin viia 2 Treffer
- myosins 2 Treffer
- ophthalmology 2 Treffer
- otorhinolaryngologic diseases 2 Treffer
- pedigree 2 Treffer
- population 2 Treffer
- retinitis pigmentosa 2 Treffer
- syndrome 2 Treffer
- usher syndromes 2 Treffer
- 3. good health 1 Treffer
- adolescent 1 Treffer
- amino acid sequence 1 Treffer
- autosomal recessive diseases 1 Treffer
- base pairing 1 Treffer
- biology and life sciences 1 Treffer
- cadherin related proteins 1 Treffer
- cadherins 1 Treffer
- child 1 Treffer
- chromosome mapping 1 Treffer
- chromosomes, human, pair 11 1 Treffer
- clinical genetics 1 Treffer
- coding region 1 Treffer
- codon, nonsense 1 Treffer
- deafness 1 Treffer
- dna 1 Treffer
- dna sequencing 1 Treffer
- dyneins 1 Treffer
- exon 1 Treffer
- eye diseases 1 Treffer
- female 1 Treffer
- founder effect 1 Treffer
- frameshift mutation 1 Treffer
- gene mapping 1 Treffer
- genetic association studies 1 Treffer
- genetic carrier screening 1 Treffer
Verlag
Publikation
4 Treffer
-
In: Ophthalmic Genetics, Jg. 32 (2011-06-15), S. 245-249Online unknownZugriff:
-
Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markersIn: Clinical Genetics, Jg. 54 (2008-06-28), S. 155-158Online unknownZugriff:
-
In: PLoS ONE, Jg. 9 (2014-09-11), S. e107326Online unknownZugriff:
-
In: Human genetics, Jg. 103 (1998-10-06), Heft 2Online unknownZugriff: