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Your search keyword '"malformazioni congenite"' showing total 2 results

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Start Over You searched for: Descriptor "malformazioni congenite" Remove constraint Descriptor: "malformazioni congenite" Topic amino acid sequence Remove constraint Topic: amino acid sequence
2 results on '"malformazioni congenite"'

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1. A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype

2. Hoxd13 and Hoxa13 directly control the expression of the EphA7 Ephrin tyrosine kinase receptor in developing limbs

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