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All mouse models of Pfeiffer syndrome with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Pfeiffer syndrome | Fgfr1tm1Led/Fgfr1tm1Led | involves: 129S4/SvJae * NIH Black Swiss | J:22118 | View | |||
| Pfeiffer syndrome | Fgfr1tm2.1Cxd/Fgfr1+ | D2.129S6(Cg)-Fgfr1tm2.1Cxd | J:228708 | View | ||||
| Pfeiffer syndrome | Fgfr2tm2.3Dsn/Fgfr2+ | involves: 129 * C57BL/6 * FVB/N | J:72517 | View | ||||