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Publikováno v:
Genetic counseling (Geneva, Switzerland). 23(4)
EEC syndrome is characterized by ectodermal dysplasia, ectrodactyly and cleft lip and/or palate and associated anomalies such as lacrimal duct obstruction, urinary tract anomaly, and hearing loss. This syndrome is a rare autosomal dominant disorder c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::420b6107785438c03736788aca2a5d6b
https://pubmed.ncbi.nlm.nih.gov/23431748
https://pubmed.ncbi.nlm.nih.gov/23431748
