Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6
Standard
Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6. / Kordes, Uwe; Mautner, Victor-Felix; Oyen, Florian; Hagel, Christian; Hartmann, Christian; Heuser, Michael; Frühwald, Michael; Hasselblatt, Martin; Oehl-Huber, Kathrin; Siebert, Reiner; Schneppenheim, Reinhard; Schüller, Ulrich.
In: PEDIATR BLOOD CANCER, Vol. 68, No. 10, 10.2021, p. e29185.Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research
Harvard
APA
Vancouver
Bibtex
}
RIS
TY - JOUR
T1 - Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6
AU - Kordes, Uwe
AU - Mautner, Victor-Felix
AU - Oyen, Florian
AU - Hagel, Christian
AU - Hartmann, Christian
AU - Heuser, Michael
AU - Frühwald, Michael
AU - Hasselblatt, Martin
AU - Oehl-Huber, Kathrin
AU - Siebert, Reiner
AU - Schneppenheim, Reinhard
AU - Schüller, Ulrich
PY - 2021/10
Y1 - 2021/10
U2 - 10.1002/pbc.29185
DO - 10.1002/pbc.29185
M3 - Other (editorial matter etc.)
C2 - 34101994
VL - 68
SP - e29185
JO - PEDIATR BLOOD CANCER
JF - PEDIATR BLOOD CANCER
SN - 1545-5009
IS - 10
ER -