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1 Ergebnisse
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Genetic and clinical characterization of a novel FH founder..:
Sánchez-Heras, Ana Beatriz
;
Dámaso, Estela
;
Castillejo, Adela
...
Orphanet Journal of Rare Diseases. 19 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/s13023-024-03017-z
RT Journal T1
Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13023-024-03017-z&Exemplar=1&LAN=DE A1 Sánchez-Heras, Ana Beatriz A1 Dámaso, Estela A1 Castillejo, Adela A1 Robledo, Mercedes A1 Teulé, Alexandre A1 Lázaro, Conxi A1 Sánchez-Martínez, Rosario A1 Zúñiga, Ángel A1 López-Fernández, Adrià A1 Balmaña, Judith A1 Robles, Luis A1 Ramon y Cajal, Teresa A1 Castillejo, M. Isabel A1 Ibañez, Raquel Perea A1 Sevila, Carmen Martínez A1 Sánchez-Mira, Andrea A1 Escandell, Inés A1 Gómez, Luís A1 Berbel, Pere A1 Soto, José Luis PB Springer Science and Business Media LLC YR 2024 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 19 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13023-024-03017-z DO https://doi.org/10.1186/s13023-024-03017-z SF ELIB - SuUB Bremen
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