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Schlagwort
- genetics 57 Treffer
- genetique 57 Treffer
- chromosome x 50 Treffer
- cromosoma x 50 Treffer
- x-chromosome 50 Treffer
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45 weitere Werte:
- homme 49 Treffer
- human 49 Treffer
- hombre 47 Treffer
- caracter ligado al sexo 45 Treffer
- caractere lie au sexe 45 Treffer
- sex linked character 45 Treffer
- enfermedad hereditaria 42 Treffer
- genetic disease 42 Treffer
- maladie hereditaire 42 Treffer
- genetique medicale 40 Treffer
- medical genetics 40 Treffer
- determinisme genetique 36 Treffer
- determinismo genetico 36 Treffer
- genetic determinism 36 Treffer
- pathogenesis 32 Treffer
- pathogenie 32 Treffer
- patogenia 32 Treffer
- gen 31 Treffer
- gene 31 Treffer
- estudio familiar 29 Treffer
- etude familiale 29 Treffer
- family study 29 Treffer
- mutacion 23 Treffer
- mutation 23 Treffer
- psychologie. psychanalyse. psychiatrie 23 Treffer
- psychology. psychoanalysis. psychiatry 23 Treffer
- psychopathologie. psychiatrie 23 Treffer
- psychopathology. psychiatry 23 Treffer
- adult and adolescent clinical studies 22 Treffer
- etude clinique de l'adulte et de l'adolescent 22 Treffer
- fenotipo 19 Treffer
- phenotype 19 Treffer
- liaison genetique 18 Treffer
- ligamiento genetico 18 Treffer
- carte genetique 16 Treffer
- genetic mapping 16 Treffer
- genetica 16 Treffer
- mapa genetico 16 Treffer
- linkage 15 Treffer
- chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) 13 Treffer
- fragilite chromosomique (syndrome de bloom, ataxie telangiectasie, anemie de fanconi, arrieration mentale liee a l'x...) 13 Treffer
- fundamental and applied biological sciences. psychology 11 Treffer
- general aspects. genetic counseling 11 Treffer
- generalites. conseil genetique 11 Treffer
- locus 11 Treffer
Verlag
- wiley-liss 31 Treffer
- bmj 7 Treffer
- blackwell 4 Treffer
- elsevier 4 Treffer
- nature publishing 4 Treffer
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9 weitere Werte:
- nature publishing group 2 Treffer
- oxford university press 2 Treffer
- societe d'edition de l'association d'enseignement medical des hopitaux de paris 2 Treffer
- society for general microbiology 2 Treffer
- university of chicago press 2 Treffer
- cambridge university press 1 Treffer
- lippincott williams & wilkins 1 Treffer
- masson 1 Treffer
- springer 1 Treffer
Publikation
- american journal of medical genetics 28 Treffer
- journal of medical genetics 7 Treffer
- x-linked mental retardation. part iii 5 Treffer
- clinical genetics 4 Treffer
- american journal of medical genetics. part a 3 Treffer
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18 weitere Werte:
- dna repair 3 Treffer
- european journal of human genetics 3 Treffer
- american journal of human genetics 2 Treffer
- annales de genetique (paris) 2 Treffer
- microbiology (reading) 2 Treffer
- nature genetics 2 Treffer
- amitochondriate protists 1 Treffer
- annals of human genetics 1 Treffer
- european journal of medical genetics 1 Treffer
- journal of antimicrobial chemotherapy (print) 1 Treffer
- mechanisms of chromosomal translocation 1 Treffer
- nature (london) 1 Treffer
- neurogenetics (oxford. print) 1 Treffer
- neurology 1 Treffer
- revue neurologique (paris) 1 Treffer
- rheumatology (oxford. print) 1 Treffer
- x-linked mental retardation 1 Treffer
- x-linked mental retardation, part i 1 Treffer
Sprache
Geographischer Bezug
64 Treffer
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In: DNA repair, Jg. 5 (2006), Heft 7, S. 840-851academicJournalZugriff:
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In: Clinical genetics, Jg. 62 (2002), Heft 6, S. 423-432Online academicJournalZugriff:
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In: Journal of antimicrobial chemotherapy (Print), Jg. 57 (2006), Heft 1, S. 31-38Online academicJournalZugriff:
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In: Amitochondriate protists, Jg. 150 (2004), S. 1439-1446Online academicJournalZugriff:
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In: European journal of human genetics, Jg. 12 (2004), Heft 1, S. 29-37Online academicJournalZugriff:
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In: Journal of medical genetics, Jg. 40 (2003), Heft 1, S. 11-17academicJournalZugriff:
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In: American journal of medical genetics, Jg. 112 (2002), Heft 1, S. 17-22Online academicJournalZugriff:
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In: American journal of medical genetics, Jg. 93 (2000), Heft 4, S. 290-293Online academicJournalZugriff:
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In: X-Linked Mental Retardation. Part III, Jg. 85 (1999), Heft 3, S. 283-287Online academicJournalZugriff:
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In: X-linked mental retardation, Jg. 97 (2000), Heft 3, S. 221-227Online academicJournalZugriff:
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In: American journal of medical genetics, Jg. 94 (2000), Heft 5, S. 364-366Online academicJournalZugriff:
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In: X-Linked Mental Retardation. Part III, Jg. 85 (1999), Heft 3, S. 263-265Online academicJournalZugriff:
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In: American journal of medical genetics, Jg. 110 (2002), Heft 4, S. 410-411Online academicJournalZugriff:
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In: European journal of human genetics, Jg. 15 (2007), Heft 1, S. 68-75Online academicJournalZugriff:
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In: Rheumatology (Oxford. Print), Jg. 46 (2007), Heft 11, S. 1667-1671Online academicJournalZugriff:
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In: DNA repair, Jg. 4 (2005), Heft 9, S. 994-1005academicJournalZugriff:
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In: American journal of medical genetics, Jg. 118A (2003), Heft 3, S. 217-222academicJournalZugriff:
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In: American journal of medical genetics, Jg. 120A (2003), Heft 4, S. 509-517academicJournalZugriff:
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In: Mechanisms of chromosomal translocation, Jg. 5 (2006), Heft 9-10, S. 1146-1160academicJournalZugriff:
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In: American journal of medical genetics. Part A, Jg. 140 (2006), Heft 6, S. 604-610Online academicJournalZugriff: