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- biology 2 Treffer
- child, preschool 2 Treffer
- chromosomes, human, x 2 Treffer
- cytogenetic analysis 2 Treffer
- gene 2 Treffer
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45 weitere Werte:
- in situ hybridization, fluorescence 2 Treffer
- medicine.disease 2 Treffer
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- mental retardation, x-linked 2 Treffer
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- phenotype 2 Treffer
- abnormalities, multiple 1 Treffer
- adolescent 1 Treffer
- arylsulfatase e 1 Treffer
- autistic disorder 1 Treffer
- business 1 Treffer
- business.industry 1 Treffer
- chondrodysplasia punctata 1 Treffer
- chromosomal proteins, non-histone 1 Treffer
- chromosome banding 1 Treffer
- chromosome breakage 1 Treffer
- chromosome deletion 1 Treffer
- chromosomes, artificial, bacterial 1 Treffer
- clone cells 1 Treffer
- developmental disabilities 1 Treffer
- developmental disorder 1 Treffer
- dna-binding proteins 1 Treffer
- education 1 Treffer
- education.field_of_study 1 Treffer
- essential tremor 1 Treffer
- family 1 Treffer
- family health 1 Treffer
- gene components 1 Treffer
- gene mapping 1 Treffer
- genetic defects of metabolism [umcn 5.1] 1 Treffer
- genetic determinism 1 Treffer
- genetic linkage 1 Treffer
- genotype 1 Treffer
- heterozygote 1 Treffer
- heterozygote advantage 1 Treffer
- infant 1 Treffer
- interleukin-1 receptor accessory protein 1 Treffer
- magnetic resonance imaging 1 Treffer
- mecp2 1 Treffer
- methyl-cpg-binding protein 2 1 Treffer
- mosaicism 1 Treffer
- multiplex ligation-dependent probe amplification 1 Treffer
- neuropsychological tests 1 Treffer
- population 1 Treffer
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In: American journal of medical genetics. Part A, 2008-11-18, Heft 24Online unknownZugriff:
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In: American journal of medical genetics. Part A, 2003-11-05, Heft 2Online unknownZugriff:
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In: American journal of medical genetics. Part A, Jg. 140 (2006-02-14), Heft 6Online unknownZugriff: