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Results 11-19 of 19 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1997
Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2
Horwitz, M.
;
Benson, K.
;
Li, F.Q.
;
Wolff, J.
;
Leppert, M.
;
Hobson, L.
;
Mangelsdorf, M.
;
Yu, S.
;
Hewett, D.
;
Richards, R.
;
Raskind, W.
1999
Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
McDermott, M.
;
Aksentijevich, I.
;
Galon, J.
;
McDermott, E.
;
Ogunkolade, B.
;
Centola, M.
;
Mansfield, E.
;
Gadina, M.
;
Karenko, L.
;
Petterson, T.
;
McCarthy, J.
;
Frucht, D.
;
Aringer, M.
;
Torosyan, Y.
;
Teppo, A.M.
;
Wilson, M.
;
Karaarslan, H.
;
Wan, Y.
;
Todd, I.
;
Wood, G.
;
et al.
1996
Identification of the gene FMR2, associated with FRAXE mental retardation
Gecz, J.
;
Gedeon, A.
;
Sutherland, G.
;
Mulley, J.
1998
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16
Cavanaugh, J.
;
Callen, D.
;
Wilson, S.
;
Stanford, P.
;
Sraml, M.
;
Gorska, M.
;
Crawford, J.
;
Whitmore, S.
;
Shlegel, C.
;
Foote, S.
;
Kohonen-Corish, M.
;
Pavli, P.
1998
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.
Town, M.
;
Jean, G.
;
Cherqui, S.
;
Attard, M.
;
Forestier, L.
;
Whitmore, S.
;
Callen, D.
;
Gribouval, O.
;
Broyer, M.
;
Bates, G.
;
van't Hoff, W.
;
Antignac, C.
1995
FRAXE and mental retardation
Mulley, J.
;
Yu, S.
;
Loesch, D.
;
Hay, D.
;
Donnelly, A.
;
Gedeon, A.
;
Carbonell, P.
;
Lopez, I.
;
Glover, G.
;
Garbarron, I.
;
Yu, P.
;
Baker, E.
;
Haan, E.
;
Hockey, A.
;
Knight, S.
;
Daview, K.
;
Richards, R.
;
Sutherland, G.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
2017
Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy
Ewans, L.J.
;
Field, M.
;
Zhu, Y.
;
Turner, G.
;
Leffler, M.
;
Dinger, M.E.
;
Cowley, M.J.
;
Buckley, M.F.
;
Scheffer, I.E.
;
Jackson, M.R.
;
Roscioli, T.
;
Shoubridge, C.
Discover
Author
10
Mulley, J.
6
Gedeon, A.
4
Colley, A.
4
Sutherland, G.
3
Gecz, J.
3
Richards, R.
3
Sillence, D.
3
Wilson, M.
2
Callen, D.
2
Phillips, H.
.
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Subject
19
Humans
17
Male
16
Female
8
Genetic Linkage
8
Molecular Sequence Data
6
Amino Acid Sequence
6
Chromosome Mapping
6
Intellectual Disability
6
X Chromosome
5
Sequence Homology, Amino Acid
.
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Date issued
2
2010 - 2019
1
2000 - 2009
16
1995 - 1999