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Issue Date
Title
Author(s)
2006
ZNF674: A new Kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation
Lugtenberg, D.
;
Yntema, H.
;
Banning, M.
;
Oudakker, A.
;
Firth, H.
;
Willatt, L.
;
Raynaud, M.
;
Kleefstra, T.
;
Fryns, J.
;
Ropers, H.
;
Chelly, J.
;
Moraine, C.
;
Gecz, J.
;
van Reeuwijk, J.
;
Nabuurs, S.
;
de Vries, B.
;
Hamel, B.
;
de Brouwer, A.
;
van Bokhoven, H.
2009
MicroRNA-regulated pathways associated with endometriosis
Ohlsson Teague, E.
;
Van Der Hoek, K.
;
Van der Hoek, M.
;
Perry, N.
;
Wagaarachchi, P.
;
Robertson, S.
;
Print, C.
;
Hull, M.
1995
Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (∆F508)
Cui, K.H.
;
Haan, E.
;
Wang, L.J.
;
Matthews, C.
2010
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families
Hynes, K.
;
Tarpey, P.
;
Dibbens, L.
;
Bayly, M.
;
Berkovic, S.
;
Smith, R.
;
Al Raisi, Z.
;
Turner, S.
;
Brown, N.
;
Desai, T.
;
Haan, E.
;
Turner, G.
;
Christodoulou, J.
;
Leonard, H.
;
Gill, D.
;
Stratton, M.
;
Gecz, J.
;
Scheffer, I.
2009
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
Spurlock, G.
;
Bennett, E.
;
Chuzhanova, N.
;
Thomas, N.
;
H-Ping, J.
;
Side, L.
;
Davies, S.
;
Haan, E.
;
Kerr, B.
;
Huson, S.
;
Upadhyaya, M.
2003
Novel PHF6 mutation p.D333del causes Borjeson-Forssman-Lehmann syndrome
Baumstark, A.
;
Lower, K.
;
Sinkus, A.
;
Andriuskeveviciute, I.
;
Jurkeniene, L.
;
Gecz, J.
;
Just, W.
2004
LGI1 mutations in temporal lobe epilepsies
Berkovic, S.
;
Izzillo, P.
;
McMahon, J.
;
Harkin, L.
;
McIntosh, A.
;
Phillips, H.
;
Briellmann, R.
;
Wallace, R.
;
Mazarib, A.
;
Neufeld, M.
;
Korczyn, A.
;
Scheffer, I.
;
Mulley, J.
2009
A Novel Bocavirus Associated with Acute Gastroenteritis in Australian Children
Arthur, J.
;
Higgins, G.
;
Davidson, G.
;
Givney, R.
;
Ratcliff, R.
;
Münger, K.
1999
Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3
Savino, M.
;
d'Apolito, M.
;
Centra, M.
;
van Beerendonk, H.
;
Cleton-Jansen, A.M.
;
Whitmore, S.
;
Crawford, J.
;
Callen, D.
;
Zelante, L.
;
Savoia, A.
2001
Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcRI-b
Hulett, M.
;
Pagler, E.
;
Hornby, J.
;
Hogarth, P.
;
Eyre, H.
;
Baker, E.
;
Crawford, J.
;
Sutherland, G.
;
Ohms, S.
;
Parish, C.
Discover
Author
15
Gecz, J.
10
Sutherland, G.
8
Haan, E.
7
et al.
5
Kalscheuer, V.
5
Ropers, H.
4
Baker, E.
4
Richards, R.
4
Scheffer, I.
4
Tarpey, P.
.
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Subject
41
Humans
33
Male
26
Base Sequence
22
Amino Acid Sequence
19
Pedigree
15
Animals
13
Mutation
10
Adult
9
Chromosome Mapping
9
DNA Mutational Analysis
.
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Date issued
6
2010 - 2014
21
2000 - 2009
15
1995 - 1999