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Publikováno v:
American Journal of Medical Genetics. 102:237-242
Ritscher-Schinzel syndrome, also known as the 3C syndrome, is a rare, autosomal recessive syndrome characterized by craniofacial, cerebellar, and cardiac anomalies. Cardiac manifestations include ventricular septal defect, atrial septal defect, tetra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a1415a5e73977fd5a8a7ad1c561811e
https://doi.org/10.1002/ajmg.1449
https://doi.org/10.1002/ajmg.1449
