Comparison of phenotypic abnormalities in Stat3 loss-of-function mice relative to Sox9 haploinsufficient mice and patients with campomelic dysplasia.
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Presence or absence of phenoypte denoted as + or -, respectively. Phenotype not investigated denoted as “N.I.”. Phenotypic information not available denoted as “unreported”.
创建时间:
2017-02-21



