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Congenital embryonal rhabdomyosarcoma caused by heterozygous concomitant PTCH1 and PTCH2 germline mutations. [electronic resource] by
- Taeubner, Julia
- Brozou, Triantafyllia
- Qin, Nan
- Bartl, Jasmin
- Ginzel, Sebastian
- Schaper, Joerg
- Felsberg, Joerg
- Fulda, Simone
- Vokuhl, Christian
- Borkhardt, Arndt
- Kuhlen, Michaela
Producer: 20181211
In:
European journal of human genetics : EJHG vol. 26
Availability: No items available.
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Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype. [electronic resource] by
- Onodera, Shoko
- Saito, Akiko
- Hasegawa, Daigo
- Morita, Nana
- Watanabe, Katsuhito
- Nomura, Takeshi
- Shibahara, Takahiko
- Ohba, Shinsuke
- Yamaguchi, Akira
- Azuma, Toshifumi
Producer: 20171012
In:
PloS one vol. 12
Availability: No items available.
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Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasms. [electronic resource] by
- Vandamme, T
- Beyens, M
- Boons, G
- Schepers, A
- Kamp, K
- Biermann, K
- Pauwels, P
- De Herder, W W
- Hofland, L J
- Peeters, M
- Van Camp, G
- Op de Beeck, K
Producer: 20200303
In:
Endocrine-related cancer vol. 26
Availability: No items available.
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