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pro vyhledávání: '"Minnis, Meenakshi"'
Autor:
Popp, Isabell, Punekar, Maqsood, Telford, Nick, Stivaros, Stavros, Chandler, Kate, Minnis, Meenakshi, Castleton, Anna, Higham, Claire, Hopewell, Louise, Gareth Evans, D., Raams, Anja, Theil, Arjan F., Meyer, Stefan, Schindler, Detlev
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
BMC Medical Genetics
Popp, I, Punekar, M, Telford, N, Stivaros, S, Chandler, K, Minnis, M, Castleton, A, Higham, C, Hopewell, L, Evans, D G, Raams, A, Theils, A F, Meyer, S & Schindler, D 2018, ' Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF ', BMC Medical Genetics . https://doi.org/10.1186/s12881-018-0520-1
BMC Medical Genetics, 19:7. BioMed Central Ltd.
BMC Medical Genetics
Popp, I, Punekar, M, Telford, N, Stivaros, S, Chandler, K, Minnis, M, Castleton, A, Higham, C, Hopewell, L, Evans, D G, Raams, A, Theils, A F, Meyer, S & Schindler, D 2018, ' Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF ', BMC Medical Genetics . https://doi.org/10.1186/s12881-018-0520-1
BMC Medical Genetics, 19:7. BioMed Central Ltd.
Background Fanconi anemia (FA) is an inherited genomic instability disorder with congenital and developmental abnormalities, bone marrow failure and predisposition to cancer early in life, and cellular sensitivity to DNA interstrand crosslinks. Case
Autor:
Popp, Isabell, Punekar, Maqsood, Telford, Nick, Stivaros, Stavros, Chandler, Kate, Minnis, Meenakshi, Castleton, Anna, Higham, Claire, Hopewell, Louise, D. Gareth Evans, Raams, Anja, Theil, Arjan, Meyer, Stefan, Schindler, Detlev
and Table S1. (DOCX 4108Â kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623124df459326b91d62fd3c61233a35