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PloS one, 2012-09, Vol.7 (9), p.e45073-e45073
2012
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The journal of clinical endocrinology and metabolism, 2008-05, Vol.93 (5), p.1865-1873
2008
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European journal of human genetics : EJHG, 2011-04, Vol.19 (4), p.492-492
2011
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American journal of human genetics, 2010-05, Vol.86 (5), p.749-764
- Miller, David T.
- Adam, Margaret P.
- Aradhya, Swaroop
- Biesecker, Leslie G.
- Brothman, Arthur R.
- Carter, Nigel P.
- Church, Deanna M.
- Crolla, John A.
- Eichler, Evan E.
- Epstein, Charles J.
- Faucett, W. Andrew
- Feuk, Lars
- Friedman, Jan M.
- Hamosh, Ada
- Jackson, Laird
- Kaminsky, Erin B.
- Kok, Klaas
- Krantz, Ian D.
- Kuhn, Robert M.
- Lee, Charles
- Ostell, James M.
- Rosenberg, Carla
- Scherer, Stephen W.
- Spinner, Nancy B.
- Stavropoulos, Dimitri J.
- Tepperberg, James H.
- Thorland, Erik C.
- Vermeesch, Joris R.
- Waggoner, Darrel J.
- Watson, Michael S.
- Martin, Christa Lese
- Ledbetter, David H.
2010
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American journal of medical genetics. Part A, 2010-08, Vol.152A (8), p.1951-1959
2010
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Prenatal diagnosis, 2013-12, Vol.33 (12), p.1119-1123
2013
Link zum Volltext
The New England journal of medicine, 2008-10, Vol.359 (16), p.1685-1699
- Mefford, Heather C
- Sharp, Andrew J
- Baker, Carl
- Itsara, Andy
- Jiang, Zhaoshi
- Buysse, Karen
- Huang, Shuwen
- Maloney, Viv K
- Crolla, John A
- Baralle, Diana
- Collins, Amanda
- Mercer, Catherine
- Norga, Koen
- de Ravel, Thomy
- Devriendt, Koen
- Bongers, Ernie M.H.F
- de Leeuw, Nicole
- Reardon, William
- Gimelli, Giorgio
- Gimelli, Stefania
- Bena, Frederique
- Hennekam, Raoul C
- Male, Alison
- Gaunt, Lorraine
- Clayton-Smith, Jill
- Simonic, Ingrid
- Park, Soo Mi
- Mehta, Sarju G
- Nik-Zainal, Serena
- Woods, C. Geoffrey
- Firth, Helen V
- Parkin, Georgina
- Fichera, Marco
- Reitano, Santina
- Giudice, Mariangela Lo
- Li, Kelly E
- Casuga, Iris
- Broomer, Adam
- Conrad, Bernard
- Schwerzmann, Markus
- Räber, Lorenz
- Gallati, Sabina
- Striano, Pasquale
- Coppola, Antonietta
- Tolmie, John L
- Tobias, Edward S
- Lilley, Chris
- Armengol, Lluis
- Spysschaert, Yves
- Verloo, Patrick
- De Coene, Anja
- Goossens, Linde
- Mortier, Geert
- Speleman, Frank
- van Binsbergen, Ellen
- Nelen, Marcel R
- Hochstenbach, Ron
- Poot, Martin
- Gallagher, Louise
- Gill, Michael
- McClellan, Jon
- King, Mary-Claire
- Regan, Regina
- Skinner, Cindy
- Stevenson, Roger E
- Antonarakis, Stylianos E
- Chen, Caifu
- Estivill, Xavier
- Menten, Björn
- Gribble, Susan
- Schwartz, Charles E
- Schwartz, Stuart
- Sutcliffe, James S
- Walsh, Tom
- Knight, Samantha J.L
- Sebat, Jonathan
- Romano, Corrado
- Veltman, Joris A
- de Vries, Bert B.A
- Vermeesch, Joris R
- Barber, John C.K
- Willatt, Lionel
- Tassabehji, May
- Eichler, Evan E
2008
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Genetics in medicine, 2011-09, Vol.13 (9), p.777-784
- Kaminsky, Erin B
- Kaul, Vineith
- Paschall, Justin
- Church, Deanna M
- Bunke, Brian
- Kunig, Dawn
- Moreno-De-Luca, Daniel
- Moreno-De-Luca, Andres
- Mulle, Jennifer G
- Warren, Stephen T
- Richard, Gabriele
- Compton, John G
- Fuller, Amy E
- Gliem, Troy J
- Huang, Shuwen
- Collinson, Morag N
- Beal, Sarah J
- Ackley, Todd
- Pickering, Diane L
- Golden, Denae M
- Aston, Emily
- Whitby, Heidi
- Shetty, Shashirekha
- Rossi, Michael R
- Rudd, M Katharine
- South, Sarah T
- Brothman, Arthur R
- Sanger, Warren G
- Iyer, Ramaswamy K
- Crolla, John A
- Thorland, Erik C
- Aradhya, Swaroop
- Ledbetter, David H
- Martin, Christa L
2011
Link zum Volltext
Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- Moreno-De-Luca, Daniel
- Mulle, Jennifer G.
- Kaminsky, Erin B.
- Sanders, Stephan J.
- Myers, Scott M.
- Adam, Margaret P.
- Pakula, Amy T.
- Eisenhauer, Nancy J.
- Uhas, Kim
- Weik, LuAnn
- Guy, Lisa
- Care, Melanie E.
- Morel, Chantal F.
- Boni, Charlotte
- Salbert, Bonnie Anne
- Chandrareddy, Ashadeep
- Demmer, Laurie A.
- Chow, Eva W.C.
- Surti, Urvashi
- Aradhya, Swaroop
- Pickering, Diane L.
- Golden, Denae M.
- Sanger, Warren G.
- Aston, Emily
- Brothman, Arthur R.
- Gliem, Troy J.
- Thorland, Erik C.
- Ackley, Todd
- Iyer, Ram
- Huang, Shuwen
- Barber, John C.
- Crolla, John A.
- Warren, Stephen T.
- Martin, Christa L.
- Ledbetter, David H.
2010
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American journal of human genetics, 2008-04, Vol.82 (4), p.927-936
2008
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American journal of human genetics, 2002-11, Vol.71 (5), p.1138-1149
2002
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American journal of human genetics, 2018-06, Vol.102 (6), p.1011-1017
2018
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European journal of human genetics : EJHG, 2012-02, Vol.20 (2), p.166-170
- NOWAKOWSKA, Beata A
- DE LEEUW, Nicole
- PFUNDT, Rolph
- MIELOO, Hanneke
- VAN ESSEN, Ton
- DE VRIES, Bert Ba
- GREEN, Andrew
- REARDON, Willie
- FRYNS, Jean-Pierre
- VERMEESCH, Joris R
- RUIVENKAMP, Claudia Al
- SIKKEMA-RADDATZ, Birgit
- CROLLA, John A
- THOELEN, Reinhilde
- KOOPMANS, Marije
- DEN HOLLANDER, Nicolette
- VAN HAERINGEN, Arie
- VAN DER KEVIE-KERSEMAEKERS, Anne-Marie
2012
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Prenatal diagnosis, 2014-01, Vol.34 (1), p.18-22
2014
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Human mutation, 2008-11, Vol.29 (11), p.E278-E283
2008
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American journal of medical genetics. Part A, 2008-03, Vol.146A (5), p.558-569
2008
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The Lancet (British edition), 2005-07, Vol.366 (9480), p.123-128
2005
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American journal of human genetics, 2005-10, Vol.77 (4), p.533-544
2005
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European journal of human genetics : EJHG, 2008-11, Vol.16 (11), p.1301-1310
2008
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American journal of medical genetics. Part A, 2014-12, Vol.164A (12), p.3194-3202
2014
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Human genetics, 2002-03, Vol.110 (3), p.244-250
2002
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European journal of human genetics : EJHG, 2012-02, Vol.20 (2), p.155-160
2012
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Journal of medical genetics, 2010-02, Vol.47 (2), p.112-115
2010
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American journal of medical genetics. Part A, 2011-07, Vol.155A (7), p.1623-1633
2011
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American journal of medical genetics. Part A, 2013-03, Vol.161A (3), p.487-500
- Barber, John C.K.
- Rosenfeld, Jill A.
- Foulds, Nicola
- Laird, Sophie
- Bateman, Mark S.
- Thomas, N. Simon
- Baker, Samantha
- Maloney, Viv K.
- Anilkumar, Arayamparambil
- Smith, Wendy E.
- Banks, Valerie
- Ellingwood, Sara
- Kharbutli, Yara
- Mehta, Lakshmi
- Eddleman, Keith A.
- Marble, Michael
- Zambrano, Regina
- Crolla, John A.
- Lamb, Allen N.
2013
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