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pro vyhledávání: '"Sriyani Basnayake"'
Autor:
Felix Kunz, Angelika Stellzig-Eisenhauer, Alina T. Midro, Yeliz Güven, Martin Zenker, Hülya Kayserili, Sriyani Basnayake, Deepthi De Silva, Agnès Bloch-Zupan, Denny Schanze, Jan Borys
Fraser syndrome (FS) is a rare autosomal recessive multiple congenital malformation syndrome characterized by cryptophthalmos, cutaneous syndactyly, renal agenesis, ambiguous genitalia, and laryngotracheal anomalies. It is caused by biallelic mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803beb0f6ed17f1cef774a7fb8c55f57
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-216147
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-216147
