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All mouse models of persistent fetal circulation syndrome with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
persistent fetal circulation syndrome | Foxf1em1Vvk/Foxf1+ | involves: C57BL/6 * DBA/2 | J:296328 | View | ||||
persistent fetal circulation syndrome | Nos3tm1Unc/Nos3tm1Unc | B6.129P2-Nos3tm1Unc/J | J:98913 | View | ||||
persistent fetal circulation syndrome |
Ptentm1Hwu/Ptentm1Hwu Twist2tm1.1(cre)Dor/Twist2+ |
B6.129-Twist2tm1.1(cre)Dor Ptentm1Hwu | J:192736 | View |