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Search Results - Wissink-Lindhout, W
Search Results - Wissink-Lindhout, W
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Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
by
Riazuddin, S
,
Hussain, M
,
Razzaq, A
,
Iqbal, Z
,
Shahzad, M
,
Polla, D L
,
Song, Y
,
van Beusekom, E
,
Khan, A A
,
Tomas-Roca, L
,
Rashid, M
,
Zahoor, M Y
,
Wissink-Lindhout, W M
,
Basra, M A R
,
Ansar, M
,
Agha, Z
,
van Heeswijk, K
,
Rasheed, F
,
Van de Vorst, M
,
Veltman, J A
,
Gilissen, C
,
Akram, J
,
Kleefstra, T
,
Assir, M Z
,
Grozeva, D
,
Carss, K
,
Raymond, F L
,
O'Connor, T D
,
Riazuddin, S A
,
Khan, S N
,
Ahmed, Z M
,
de Brouwer, A P M
,
van Bokhoven, H
,
Riazuddin, S
Published in
Molecular psychiatry
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Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
by
Riazuddin, S
,
Hussain, M
,
Razzaq, A
,
Iqbal, Z
,
Shahzad, M
,
Polla, D L
,
Song, Y
,
van Beusekom, E
,
Khan, A A
,
Tomas-Roca, L
,
Rashid, M
,
Zahoor, M Y
,
Wissink-Lindhout, W M
,
Basra, M A R
,
Ansar, M
,
Agha, Z
,
van Heeswijk, K
,
Rasheed, F
,
Van de Vorst, M
,
Veltman, J A
,
Gilissen, C
,
Akram, J
,
Kleefstra, T
,
Assir, M Z
,
Grozeva, D
,
Carss, K
,
Raymond, F L
,
O'Connor, T D
,
Riazuddin, S A
,
Khan, S N
,
Ahmed, Z M
,
de Brouwer, A P M
,
van Bokhoven, H
,
Riazuddin, S
Published in
Molecular psychiatry
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Update on Kleefstra Syndrome
by
Willemsen, M.H.
,
Vulto-van Silfhout, A.T.
,
Nillesen, W.M.
,
Wissink-Lindhout, W.M.
,
van Bokhoven, H.
,
Philip, N.
,
Berry-Kravis, E.M.
,
Kini, U.
,
van Ravenswaaij-Arts, C.M.A.
,
Delle Chiaie, B.
,
Innes, A.M.M.
,
Houge, G.
,
Kosonen, T.
,
Cremer, K.
,
Fannemel, M.
,
Stray-Pedersen, A.
,
Reardon, W.
,
Ignatius, J.
,
Lachlan, K.
,
Mircher, C.
,
Helderman van den Enden, P.T.J.M.
,
Mastebroek, M.
,
Cohn-Hokke, P.E.
,
Yntema, H.G.
,
Drunat, S.
,
Kleefstra, T.
Published in
Molecular syndromology
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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
by
Hu, H
,
Haas, S A
,
Chelly, J
,
Van Esch, H
,
Raynaud, M
,
de Brouwer, A P M
,
Weinert, S
,
Froyen, G
,
Frints, S G M
,
Laumonnier, F
,
Zemojtel, T
,
Love, M I
,
Richard, H
,
Emde, A-K
,
Bienek, M
,
Jensen, C
,
Hambrock, M
,
Fischer, U
,
Langnick, C
,
Feldkamp, M
,
Wissink-Lindhout, W
,
Lebrun, N
,
Castelnau, L
,
Rucci, J
,
Montjean, R
,
Dorseuil, O
,
Billuart, P
,
Stuhlmann, T
,
Shaw, M
,
Corbett, M A
,
Gardner, A
,
Willis-Owen, S
,
Tan, C
,
Friend, K L
,
Belet, S
,
van Roozendaal, K E P
,
Jimenez-Pocquet, M
,
Moizard, M-P
,
Ronce, N
,
Sun, R
,
O'Keeffe, S
,
Chenna, R
,
van Bömmel, A
,
Göke, J
,
Hackett, A
,
Field, M
,
Christie, L
,
Boyle, J
,
Haan, E
,
Nelson, J
,
Turner, G
,
Baynam, G
,
Gillessen-Kaesbach, G
,
Müller, U
,
Steinberger, D
,
Budny, B
,
Badura-Stronka, M
,
Latos-Bieleńska, A
,
Ousager, L B
,
Wieacker, P
,
Rodríguez Criado, G
,
Bondeson, M-L
,
Annerén, G
,
Dufke, A
,
Cohen, M
,
Van Maldergem, L
,
Vincent-Delorme, C
,
Echenne, B
,
Simon-Bouy, B
,
Kleefstra, T
,
Willemsen, M
,
Fryns, J-P
,
Devriendt, K
,
Ullmann, R
,
Vingron, M
,
Wrogemann, K
,
Wienker, T F
,
Tzschach, A
,
van Bokhoven, H
,
Gecz, J
,
Jentsch, T J
,
Chen, W
,
Ropers, H-H
,
Kalscheuer, V M
Published in
Molecular psychiatry
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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
by
Snijders Blok, Lot
,
Madsen, Erik
,
Juusola, Jane
,
Gilissen, Christian
,
Baralle, Diana
,
Reijnders, Margot R.F.
,
Venselaar, Hanka
,
Helsmoortel, Céline
,
Cho, Megan T.
,
Hoischen, Alexander
,
Vissers, Lisenka E.L.M.
,
Koemans, Tom S.
,
Wissink-Lindhout, Willemijn
,
Eichler, Evan E.
,
Romano, Corrado
,
Van Esch, Hilde
,
Stumpel, Connie
,
Vreeburg, Maaike
,
Smeets, Eric
,
Oberndorff, Karin
,
van Bon, Bregje W.M.
,
Shaw, Marie
,
Gecz, Jozef
,
Haan, Eric
,
Bienek, Melanie
,
Jensen, Corinna
,
Loeys, Bart L.
,
Van Dijck, Anke
,
Innes, A. Micheil
,
Racher, Hilary
,
Vermeer, Sascha
,
Di Donato, Nataliya
,
Rump, Andreas
,
Tatton-Brown, Katrina
,
Parker, Michael J.
,
Henderson, Alex
,
Lynch, Sally A.
,
Fryer, Alan
,
Ross, Alison
,
Vasudevan, Pradeep
,
Kini, Usha
,
Newbury-Ecob, Ruth
,
Chandler, Kate
,
Male, Alison
,
Dijkstra, Sybe
,
Schieving, Jolanda
,
Giltay, Jacques
,
van Gassen, Koen L.I.
,
Schuurs-Hoeijmakers, Janneke
,
Tan, Perciliz L.
,
Pediaditakis, Igor
,
Haas, Stefan A.
,
Retterer, Kyle
,
Reed, Patrick
,
Monaghan, Kristin G.
,
Haverfield, Eden
,
Natowicz, Marvin
,
Myers, Angela
,
Kruer, Michael C.
,
Stein, Quinn
,
Strauss, Kevin A.
,
Brigatti, Karlla W.
,
Keating, Katherine
,
Burton, Barbara K.
,
Kim, Katherine H.
,
Charrow, Joel
,
Norman, Jennifer
,
Foster-Barber, Audrey
,
Kline, Antonie D.
,
Kimball, Amy
,
Zackai, Elaine
,
Harr, Margaret
,
Fox, Joyce
,
McLaughlin, Julie
,
Lindstrom, Kristin
,
Haude, Katrina M.
,
van Roozendaal, Kees
,
Brunner, Han
,
Chung, Wendy K.
,
Kooy, R. Frank
,
Pfundt, Rolph
,
Kalscheuer, Vera
,
Mehta, Sarju G.
,
Katsanis, Nicholas
,
Kleefstra, Tjitske
Published in
American journal of human genetics
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