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pro vyhledávání: '"Miluše Vilémová"'
Autor:
Ivana Slámová, Petr Kuglík, Miluše Vilémová, Jana Šoukalová, Eva Zrnová, Renata Gaillyová, Vladimíra Vranová
Publikováno v:
Molecular Syndromology. 2:88-93
We report an infant with a unique combination of 22q11 deletion syndrome and 14q terminal deletion syndrome. The proband had clinical symptoms compatible with diagnosis of 22q11 deletion syndrome: microcephaly, micrognathia, high-arched palate, hyper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55448139ed0aab7be0dae23c2b939a0c
https://doi.org/10.1159/000335334
https://doi.org/10.1159/000335334
