The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome
収録刊行物
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- Human Molecular Genetics
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Human Molecular Genetics 7 (6), 945-957, 1998-06-01
Oxford University Press (OUP)
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詳細情報 詳細情報について
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- CRID
- 1361418520936899712
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- NII論文ID
- 30018400839
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- ISSN
- 14602083
- http://id.crossref.org/issn/09646906
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- データソース種別
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- Crossref
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