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Typical 22q11.2 deletion syndrome appears to confer a reduc..:
Evans, D. Gareth
;
Messiaen, Ludwine M.
;
Foulkes, William D.
...
Genetics in Medicine. 23 (2021) 9 - p. 1779-1782 , 2021
Link:
https://doi.org/10.1038/s41436-021-01175-0
RT Journal T1
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41436-021-01175-0&Exemplar=1&LAN=DE A1 Evans, D. Gareth A1 Messiaen, Ludwine M. A1 Foulkes, William D. A1 Irving, Rachel E.A. A1 Murray, Alexandra J. A1 Perez-Becerril, Cristina A1 Rivera, Barbara A1 McDonald-McGinn, Donna M. A1 Stevenson, David A. A1 Smith, Miriam J. PB Elsevier BV YR 2021 SN 1098-3600 JF Genetics in Medicine VO 23 IS 9 SP 1779 OP 1782 LK http://dx.doi.org/https://doi.org/10.1038/s41436-021-01175-0 DO https://doi.org/10.1038/s41436-021-01175-0 SF ELIB - SuUB Bremen
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