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- usher syndrome 4 Treffer
- linkage 3 Treffer
- myo7a 3 Treffer
- chromosome mapping 2 Treffer
- chromosomes, human, pair 11 2 Treffer
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45 weitere Werte:
- deafness 2 Treffer
- genetics 2 Treffer
- homozygosity 2 Treffer
- microsatellite repeats 2 Treffer
- myosins 2 Treffer
- biological and medical sciences 1 Treffer
- biology 1 Treffer
- carte genetique 1 Treffer
- chromosome c11 1 Treffer
- chromosome-1q 1 Treffer
- complex syndromes 1 Treffer
- cromosoma c11 1 Treffer
- determinisme genetique 1 Treffer
- determinismo genetico 1 Treffer
- diagnosis 1 Treffer
- diagnostic 1 Treffer
- diagnostico 1 Treffer
- dyneins 1 Treffer
- enfermedad hereditaria 1 Treffer
- ent disease 1 Treffer
- exon 1 Treffer
- eye disease 1 Treffer
- families 1 Treffer
- gene 1 Treffer
- gene mapping 1 Treffer
- genetic carrier screening 1 Treffer
- genetic determinism 1 Treffer
- genetic disease 1 Treffer
- genetic linkage 1 Treffer
- genetic mapping 1 Treffer
- genetica 1 Treffer
- genetics (clinical) 1 Treffer
- genetique 1 Treffer
- genetique medicale 1 Treffer
- heterogeneity 1 Treffer
- heterozigosis 1 Treffer
- heterozygosity 1 Treffer
- heterozygotie 1 Treffer
- hombre 1 Treffer
- homme 1 Treffer
- human 1 Treffer
- humans 1 Treffer
- liaison genetique 1 Treffer
- ligamiento genetico 1 Treffer
- locus 1 Treffer
Verlag
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4 Treffer
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Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markersIn: Clinical genetics, Jg. 54 (1998), Heft 2, S. 155-158Online academicJournalZugriff:
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Map refinement of the Usher syndrome type IB gene, MYO7A, relative to 11q13.5 microsatellite markersIn: CLINICAL GENETICS, Jg. 54 (1998), Heft 2, S. 155-158Online serialPeriodicalZugriff:
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Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markersIn: Clinical Genetics, Jg. 54 (1998-08-01), Heft 2, S. 155-156Online academicJournal
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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: