IDENTIFICATION OF LIMB DEFECTS IN MOUSE EMBRYOS LACKING FGF2IIIB WITH OCT/MRI

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 我们将通过结合光学CT（OCT）和MRM信息研究缺乏Fgfr 2 IIIb的小鼠胚胎标本的肢体缺陷。将对样本进行染色以进行MR成像，然后使用阿辛蓝染色剂对软骨进行染色，并进行OCT成像。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. We will study limb defects in specimen mouse embryos lacking Fgfr2IIIb by combining optical CT (OCT) and MRM information. Specimens will be stained for MR imaging, then stained for cartilage using alcian blue stain and cleared for OCT imaging.