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Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma. [electronic resource] by
- Slade, Ingrid
- Murray, Anne
- Hanks, Sandra
- Kumar, Ajith
- Walker, Lisa
- Hargrave, Darren
- Douglas, Jenny
- Stiller, Charles
- Izatt, Louise
- Rahman, Nazneen
Producer: 20111003
In:
Familial cancer vol. 10
Availability: No items available.
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Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations. [electronic resource] by
- Smith, Miriam J
- Beetz, Christian
- Williams, Simon G
- Bhaskar, Sanjeev S
- O'Sullivan, James
- Anderson, Beverley
- Daly, Sarah B
- Urquhart, Jill E
- Bholah, Zaynab
- Oudit, Deemesh
- Cheesman, Edmund
- Kelsey, Anna
- McCabe, Martin G
- Newman, William G
- Evans, D Gareth R
Producer: 20150223
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 32
Availability: No items available.
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