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<i>FOXF1</i> gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical review

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPathogenesisClinical ReviewPathologyMolecular GeneticsMedical GeneticsAlveolar Capillary DysplasiaDisease Gene IdentificationMedicineConnective Tissue Disease