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Issue Date
Title
Author(s)
2016
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
van Bon, B.W.M.
;
Coe, B.P.
;
Bernier, R.
;
Green, C.
;
Gerdts, J.
;
Witherspoon, K.
;
Kleefstra, T.
;
Willemsen, M.H.
;
Kumar, R.
;
Bosco, P.
;
Fichera, M.
;
Li, D.
;
Amaral, D.
;
Cristofoli, F.
;
Peeters, H.
;
Haan, E.
;
Romano, C.
;
Mefford, H.C.
;
Scheffer, I.
;
Gecz, J.
;
et al.
2016
Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders
Moey, C.
;
Hinze, S.
;
Brueton, L.
;
Morton, J.
;
McMullan, D.
;
Kamien, B.
;
Barnett, C.
;
Brunetti-Pierri, N.
;
Nicholl, J.
;
Gecz, J.
;
Shoubridge, C.
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.
2016
Prenatal and familial factors of caries in first permanent molars in schoolchildren living in urban area of Łódź, Poland
Borowska-Strugińska, B.
;
Żądzińska, E.
;
Bruzda-Zwiech, A.
;
Filipińska, R.
;
Lubowiecka-Gontarek, B.
;
Szydłowska-Walendowska, B.
;
Wochna-Sobańska, M.
2016
Characterization of leukemias with ETV6-ABL1 fusion
Zaliova, M.
;
Moorman, A.V.
;
Cazzaniga, G.
;
Stanulla, M.
;
Harvey, R.C.
;
Roberts, K.G.
;
Heatley, S.L.
;
Loh, M.L.
;
Konopleva, M.
;
Chen, I.M.
;
Zimmermannova, O.
;
Schwab, C.
;
Smith, O.
;
Mozziconacci, M.J.
;
Chabannon, C.
;
Kim, M.
;
Frederik Falkenburg, J.H.
;
Norton, A.
;
Marshall, K.
;
Haas, O.A.
;
et al.
;
Annual Meeting of the American-Society-of-Hematology (5 Dec 2015 - 8 Dec 2015 : Orlando, FL)
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Author
3
et al.
2
Gecz, J.
2
Schwab, C.
1
Amaral, D.
1
Annual Meeting of the American-So...
1
Barnett, C.
1
Bernier, R.
1
Borowska-Strugińska, B.
1
Bosco, P.
1
Brueton, L.
.
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Child
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Humans
5
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3
Infant
3
Young Adult
2
Adult
2
Cohort Studies
2
DNA Copy Number Variations
2
Intellectual Disability
2
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