Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family
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| Veröffentlicht in: | NPJ genomic medicine 2018, Vol.3, p.35-35 |
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| container_end_page | 35 |
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| container_issue | |
| container_start_page | 35 |
| container_title | NPJ genomic medicine |
| container_volume | 3 |
| creator | AlHarbi, Musa Mubarak, Nahla AlMubarak, Latifa Aljelaify, Rasha AlSaeed, Mariam Almutairi, Amal AlJabarat, Weal Alqubaishi, Fatimah Al-Subaie, Lamia AlTassan, Nada Neben, Cynthia L Zhou, Alicia Y Abedalthagafi, Malak |
| description | |
| doi_str_mv | 10.1038/s41525-018-0074-3 |
| format | Report |
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| identifier | EISSN: 2056-7944 |
| ispartof | NPJ genomic medicine, 2018, Vol.3, p.35-35 |
| issn | 2056-7944 |
| language | eng |
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| source | Nature Free; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access; Springer Nature OA Free Journals |
| title | Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi family |
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