这是遗传学. 设计一个破碎的心脏.

P J Scambler

Nature

|October 12, 1999

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这是遗传学. 设计一个破碎的心脏.

相关概念视频

Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice.

Molecular study of 33 families with Fraser syndrome new data and mutation review.

Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13.

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.

Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.

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相关实验视频

这是遗传学. 设计一个破碎的心脏.

相关概念视频

Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice.

Molecular study of 33 families with Fraser syndrome new data and mutation review.

Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.

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Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.

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Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

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