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Issue Date
Title
Author(s)
2016
TBC1D24 genotype-phenotype correlation
Balestrini, S.
;
Milh, M.
;
Castiglioni, C.
;
Lüthy, K.
;
Finelli, M.
;
Verstreken, P.
;
Cardon, A.
;
Stražišar, B.
;
Holder, J.
;
Lesca, G.
;
Mancardi, M.
;
Poulat, A.
;
Repetto, G.
;
Banka, S.
;
Bilo, L.
;
Birkeland, L.
;
Bosch, F.
;
Brockmann, K.
;
Cross, J.
;
Doummar, D.
;
et al.
2016
A genome-wide association study in multiple system atrophy
Sailer, A.
;
Scholz, S.W.
;
Nalls, M.A.
;
Schulte, C.
;
Federoff, M.
;
Price, T.R.
;
Lees, A.
;
Ross, O.A.
;
Dickson, D.W.
;
Mok, K.
;
Mencacci, N.E.
;
Schottlaender, L.
;
Chelban, V.
;
Ling, H.
;
O'Sullivan, S.S.
;
Wood, N.W.
;
Traynor, B.J.
;
Ferrucci, L.
;
Federoff, H.J.
;
Mhyre, T.R.
;
et al.
2016
Multiplex families with epilepsy: success of clinical and molecular genetic characterization
Afawi, Z.
;
Oliver, K.L.
;
Kivity, S.
;
Mazarib, A.
;
Blatt, I.
;
Neufeld, M.Y.
;
Helbig, K.L.
;
Goldberg-Stern, H.
;
Misk, A.J.
;
Straussberg, R.
;
Walid, S.
;
Mahajnah, M.
;
Lerman-Sagie, T.
;
Ben-Zeev, B.
;
Kahana, E.
;
Masalha, R.
;
Kramer, U.
;
Ekstein, D.
;
Shorer, Z.
;
Wallace, R.H.
;
et al.
2016
Integration of genetic and clinical risk factors improves prognostication in relapsed childhood B-cell precursor acute lymphoblastic leukemia
Irving, J.
;
Enshaei, A.
;
Parker, C.
;
Sutton, R.
;
Kuiper, R.
;
Erhorn, A.
;
Minto, L.
;
Venn, N.
;
Law, T.
;
Yu, J.
;
Schwab, C.
;
Davies, R.
;
Matheson, E.
;
Davies, A.
;
Sonneveld, E.
;
Den Boer, M.
;
Love, S.
;
Harrison, C.
;
Hoogerbrugge, P.
;
Revesz, T.
;
et al.
Discover
Author
1
Afawi, Z.
1
Balestrini, S.
1
Banka, S.
1
Ben-Zeev, B.
1
Bilo, L.
1
Birkeland, L.
1
Blatt, I.
1
Bosch, F.
1
Brockmann, K.
1
Cardon, A.
.
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Subject
4
Humans
3
Female
3
Male
2
Brain
2
Child
2
Child, Preschool
2
Epilepsy
2
Genetic Predisposition to Disease
2
Infant
2
Mutation
.
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