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- amino acid substitution 1 Treffer
- androgen binding 1 Treffer
- androgen insensitivity syndrome 1 Treffer
- androgen receptor 1 Treffer
- animals 1 Treffer
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37 weitere Werte:
- base sequence 1 Treffer
- biochemistry 1 Treffer
- cells, cultured 1 Treffer
- chemistry 1 Treffer
- chemistry.chemical_classification 1 Treffer
- cholesterol ester storage disease 1 Treffer
- compound heterozygosity 1 Treffer
- ddc:618 1 Treffer
- dna primers 1 Treffer
- endocrinology 1 Treffer
- enzyme 1 Treffer
- female 1 Treffer
- gene 1 Treffer
- genotype 1 Treffer
- gynecomastia 1 Treffer
- heterozygote 1 Treffer
- histidine 1 Treffer
- humans 1 Treffer
- insecta 1 Treffer
- insects 1 Treffer
- internal medicine 1 Treffer
- lipase 1 Treffer
- lysosomes 1 Treffer
- male 1 Treffer
- medicine.disease 1 Treffer
- medicine.disease_cause 1 Treffer
- medicine.medical_specialty 1 Treffer
- missense mutation 1 Treffer
- molecular biology 1 Treffer
- mutation 1 Treffer
- partial androgen insensitivity syndrome 1 Treffer
- phenotype 1 Treffer
- proline 1 Treffer
- rna splicing 1 Treffer
- transition (genetics) 1 Treffer
- undervirilization 1 Treffer
- urologic and male genital diseases 1 Treffer
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In: Human mutation, Jg. 12 (1998-06-20), Heft 1Online unknownZugriff:
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In: Human Mutation, Jg. 14 (1999-10-01), S. 353-353Online unknownZugriff: