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- chromosome 2 Treffer
- chromosome mapping 2 Treffer
- deafness 2 Treffer
- female 2 Treffer
- gene mapping 2 Treffer
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- genes, recessive 2 Treffer
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- sensorineural hearing loss 2 Treffer
- adolescent 1 Treffer
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- biology.protein 1 Treffer
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- chromosomes, human, pair 10 1 Treffer
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- gene 1 Treffer
- genetic markers 1 Treffer
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- hearing loss 1 Treffer
- hearing loss, sensorineural 1 Treffer
- infant 1 Treffer
- locus (genetics) 1 Treffer
- medicine.symptom 1 Treffer
- molecular sequence data 1 Treffer
- mutant 1 Treffer
- new zealand 1 Treffer
- nonsyndromic deafness 1 Treffer
- population 1 Treffer
- prelingual deafness 1 Treffer
- prevalence 1 Treffer
- sequence deletion 1 Treffer
- syria 1 Treffer
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- united kingdom 1 Treffer
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In: Human Molecular Genetics, Jg. 6 (1997-11-01), S. 2173-2177Online unknownZugriff:
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In: Human molecular genetics, Jg. 5 (1996-07-01), Heft 7Online unknownZugriff:
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In: Human molecular genetics, Jg. 5 (1996), Heft 1Online unknownZugriff: