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Issue Date
Title
Author(s)
2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Cundy, T.
;
Hegde, M.
;
Naot, D.
;
Chong, B.
;
King, A.
;
Wallace, R.
;
Mulley, J.
;
Love, D.
;
Seidel, J.
;
Fawkner, M.
;
Banovic, T.
;
Callon, K.
;
Grey, A.
;
Reid, I.
;
Middleton-Hardie, C.
;
Cornish, J.
1995
Detection of circulating tumor cells in colorectal cancer by Immunobead-PCR is a sensitive prognostic marker for relapse of disease
Hardingham, J.
;
Kotasek, D.
;
Sage, R.
;
Eaton, M.
;
Pascoe, V.
;
Dobrovic, A.
2019
GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon
Tingang Wonkam, E.
;
Chimusa, E.
;
Noubiap, J.J.
;
Adadey, S.M.
;
F Fokouo, J.V.
;
Wonkam, A.
1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Colley, A.
;
Jamieson, R.
;
Thompson, E.
;
Rogers, J.
;
Sillence, D.
;
Tiller, G.
;
Mulley, J.
;
Gecz, J.
2023
TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms
Shah, M.V.
;
Tran, E.N.H.
;
Shah, S.
;
Chhetri, R.
;
Baranwal, A.
;
Ladon, D.
;
Shultz, C.
;
Al-Kali, A.
;
Brown, A.L.
;
Chen, D.
;
Scott, H.S.
;
Greipp, P.
;
Thomas, D.
;
Alkhateeb, H.B.
;
Singhal, D.
;
Gangat, N.
;
Kumar, S.
;
Patnaik, M.M.
;
Hahn, C.N.
;
Kok, C.H.
;
et al.
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
2012
Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial
Falchook, G.
;
Long, G.
;
Kurzrock, R.
;
Kim, K.
;
Arkenau, T.
;
Brown, M.
;
Hamid, O.
;
Infante, J.
;
Millward, M.
;
Pavlick, A.
;
O'Day, S.
;
Blackman, S.
;
Curtis, C.
;
Lebowitz, P.
;
Ma, B.
;
Ouellet, D.
;
Kefford, R.
2006
Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults
Jansen, F.
;
Sadleir, L.
;
Harkin, L.
;
Vadlamudi, L.
;
McMahon, J.
;
Mulley, J.
;
Scheffer, I.
;
Berkovic, S.
2011
Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndrome
Drini, M.
;
Wong, N.
;
Scott, H.
;
Craig, J.
;
Dobrovic, A.
;
Hewitt, C.
;
Dow, C.
;
Young, J.
;
Jenkins, M.
;
Saffery, R.
;
Macrae, F.
;
Oshima, R.
Discover
Author
3
Mulley, J.
2
Dobrovic, A.
2
et al.
1
Adadey, S.M.
1
Al-Kali, A.
1
Alkhateeb, H.B.
1
Arkenau, T.
1
Banovic, T.
1
Baranwal, A.
1
Bellows, S.
.
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Colorectal Neoplasms
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Genetic Predisposition to Disease
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Date issued
1
2020 - 2023
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2010 - 2019
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2000 - 2009
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1995 - 1999