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Autor:
Kaymakçalan, H., Kaya, İlyas, Kaya, İ., Binici, N. C., Nikerel, E., Özbaran, B., Aksoy, M. G., Erbilen, S., Özyurt, G., Jahan, N., Çelik, D., Yarabaş, K., Yalçınkaya, Leyla, Durak, S., Köse, S., Şençiçek, A. G. E.
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Background: Phosphatase and tensin homolog (PTEN) germline mutations are associated with cancer syndromes (PTEN hamartoma tumor syndrome; PHTS) and in pediatric patients with autism spectrum disorder (ASD) and macrocephaly. The exact prevalence of PT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8f89512637232f3bda94dd30e6a9dda
https://hdl.handle.net/11693/77437
https://hdl.handle.net/11693/77437
