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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...PloS one, 2022-11, Vol.17 (11), p.e0268149-e0268149
- Hall, Hildegard Nikki
- Bengani, Hemant
- Hufnagel, Robert B
- Damante, Giuseppe
- Ansari, Morad
- Marsh, Joseph A
- Grimes, Graeme R
- Kriegsheim, Alex von
- Moore, David
- McKie, Lisa
- Rahmat, Jamalia
- Mio, Catia
- Blyth, Moira
- Keng, Wee Teik
- Islam, Lily
- McEntargart, Meriel
- Mannens, Marcel M
- Heyningen, Veronica Van
- Rainger, Joe
- Brooks, Brian P
- FitzPatrick, David R
- Swaroop, Anand
2022
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Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate
2016
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Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1013-n/a
2020
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American journal of human genetics, 2017-11, Vol.101 (5), p.664-685
- Myers, Candace T.
- Cossette, Patrick
- Lemay, Philippe
- Spiegelman, Dan
- Laporte, Alexandre Dionne
- Nassif, Christina
- Diallo, Ousmane
- Monlong, Jean
- Cadieux-Dion, Maxime
- Dobrzeniecka, Sylvia
- Meloche, Caroline
- Retterer, Kyle
- Cho, Megan T.
- Rosenfeld, Jill A.
- Bi, Weimin
- Massicotte, Christine
- Miguet, Marguerite
- Brunga, Ledia
- Regan, Brigid M.
- Mo, Kelly
- Tam, Cory
- Hollingsworth, Georgie
- FitzPatrick, David R.
- Canham, Natalie
- Blair, Edward
- Kerr, Bronwyn
- Fry, Andrew E.
- Thomas, Rhys H.
- Shelagh, Joss
- Hurst, Jane A.
- Brittain, Helen
- Blyth, Moira
- Lebel, Robert Roger
- Gerkes, Erica H.
- Davis-Keppen, Laura
- Stein, Quinn
- Dorison, Sara J.
- Benke, Paul J.
- Fassi, Emily
- Corsten-Janssen, Nicole
- Kamsteeg, Erik-Jan
- Mau-Them, Frederic T.
- Bruel, Ange-Line
- Verloes, Alain
- Õunap, Katrin
- Wojcik, Monica H.
- Albert, Dara V.F.
- Venkateswaran, Sunita
- Ware, Tyson
- Liu, Yu-Chi
- Mohammad, Shekeeb S.
- Bizargity, Peyman
- Bacino, Carlos A.
- Leuzzi, Vincenzo
- Martinelli, Simone
- Dallapiccola, Bruno
- Tartaglia, Marco
- Blumkin, Lubov
- Wierenga, Klaas J.
- Purcarin, Gabriela
- O’Byrne, James J.
- Stockler, Sylvia
- Lehman, Anna
- Keren, Boris
- Nougues, Marie-Christine
- Mignot, Cyril
- Auvin, Stéphane
- Nava, Caroline
- Hiatt, Susan M.
- Bebin, Martina
- Shao, Yunru
- Scaglia, Fernando
- Frye, Richard E.
- Jarjour, Imad T.
- Jacques, Stéphanie
- Boucher, Renee-Myriam
- Riou, Emilie
- Srour, Myriam
- Carmant, Lionel
- Lortie, Anne
- Major, Philippe
- Diadori, Paola
- Dubeau, François
- D’Anjou, Guy
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- Berkovic, Samuel F.
- Sadleir, Lynette G.
- Campeau, Philippe M.
- Kibar, Zoha
- Lafrenière, Ronald G.
- Girard, Simon L.
- Mercimek-Mahmutoglu, Saadet
- Boelman, Cyrus
- Rouleau, Guy A.
- Scheffer, Ingrid E.
- Mefford, Heather C.
- Andrade, Danielle M.
- Rossignol, Elsa
- Minassian, Berge A.
- Michaud, Jacques L.
2017
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Journal of clinical sleep medicine, 2017-11, Vol.13 (11), p.1359-1362
2017
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Journal of medical genetics, 2015-07, Vol.52 (7), p.454-464
2015
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Nature genetics, 2015-11, Vol.47 (11), p.1363-1369
- Akawi, Nadia
- McRae, Jeremy
- Ansari, Morad
- Balasubramanian, Meena
- Blyth, Moira
- Brady, Angela F
- Clayton, Stephen
- Cole, Trevor
- Deshpande, Charu
- Fitzgerald, Tomas W
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- Goodship, Judith
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- Joss, Shelagh
- King, Daniel
- Klena, Nikolai
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- McMullan, Dominic
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- Wright, Caroline F
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- Barrett, Jeffrey C
- Lo, Cecilia W
- FitzPatrick, David R
- Hurles, Matthew E
2015
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Journal of medical genetics, 2016-03, Vol.53 (3), p.152-162
- Hempel, Annmarie
- Pagnamenta, Alistair T
- Blyth, Moira
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- Ikegawa, Shiro
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- Matsumoto, Naomichi
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- Plessis, Ghislaine
- Albrecht, Beate
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- Howard, Malcolm F
- Keays, David
- Sohal, Aman Singh
- Kühl, Susanne J
- Kini, Usha
- McNeill, Alisdair
2016
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The Journal of clinical investigation, 2023-05, Vol.133 (10), p.1-16
- Gehin, Charlotte
- Lone, Museer A
- Lee, Winston
- Capolupo, Laura
- Ho, Sylvia
- Adeyemi, Adekemi M
- Gerkes, Erica H
- Stegmann, Alexander Pa
- López-Martín, Estrella
- Bermejo-Sánchez, Eva
- Martínez-Delgado, Beatriz
- Zweier, Christiane
- Kraus, Cornelia
- Popp, Bernt
- Strehlow, Vincent
- Gräfe, Daniel
- Knerr, Ina
- Jones, Eppie R
- Zamuner, Stefano
- Abriata, Luciano A
- Kunnathully, Vidya
- Moeller, Brandon E
- Vocat, Anthony
- Rommelaere, Samuel
- Bocquete, Jean-Philippe
- Ruchti, Evelyne
- Limoni, Greta
- Van Campenhoudt, Marine
- Bourgeat, Samuel
- Henklein, Petra
- Gilissen, Christian
- van Bon, Bregje W
- Pfundt, Rolph
- Willemsen, Marjolein H
- Schieving, Jolanda H
- Leonardi, Emanuela
- Soli, Fiorenza
- Murgia, Alessandra
- Guo, Hui
- Zhang, Qiumeng
- Xia, Kun
- Fagerberg, Christina R
- Beier, Christoph P
- Larsen, Martin J
- Valenzuela, Irene
- Fernández-Álvarez, Paula
- Xiong, Shiyi
- Śmigiel, Robert
- López-González, Vanesa
- Armengol, Lluís
- Morleo, Manuela
- Selicorni, Angelo
- Torella, Annalaura
- Blyth, Moira
- Cooper, Nicola S
- Wilson, Valerie
- Oegema, Renske
- Herenger, Yvan
- Garde, Aurore
- Bruel, Ange-Line
- Tran Mau-Them, Frederic
- Maddocks, Alexis Br
- Bain, Jennifer M
- Bhat, Musadiq A
- Costain, Gregory
- Kannu, Peter
- Marwaha, Ashish
- Champaigne, Neena L
- Friez, Michael J
- Richardson, Ellen B
- Gowda, Vykuntaraju K
- Srinivasan, Varunvenkat M
- Gupta, Yask
- Lim, Tze Y
- Sanna-Cherchi, Simone
- Lemaitre, Bruno
- Yamaji, Toshiyuki
- Hanada, Kentaro
- Burke, John E
- Jakšić, Ana Marjia
- McCabe, Brian D
- De Los Rios, Paolo
- Hornemann, Thorsten
- D'Angelo, Giovanni
- Gennarino, Vincenzo A
2023
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Journal of genetic counseling, 2020-04, Vol.29 (2), p.282-292
2020
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American journal of human genetics, 2023-11, Vol.110 (11), p.1919-1937
- Nil, Zelha
- Deshwar, Ashish R.
- Huang, Yan
- Barish, Scott
- Zhang, Xi
- Choufani, Sanaa
- Le Quesne Stabej, Polona
- Hayes, Ian
- Yap, Patrick
- Haldeman-Englert, Chad
- Wilson, Carolyn
- Prescott, Trine
- Tveten, Kristian
- Vøllo, Arve
- Haynes, Devon
- Wheeler, Patricia G.
- Zon, Jessica
- Cytrynbaum, Cheryl
- Jobling, Rebekah
- Blyth, Moira
- Banka, Siddharth
- Afenjar, Alexandra
- Mignot, Cyril
- Robin-Renaldo, Florence
- Keren, Boris
- Kanca, Oguz
- Mao, Xiao
- Wegner, Daniel J.
- Sisco, Kathleen
- Shinawi, Marwan
- Wangler, Michael F.
- Weksberg, Rosanna
- Yamamoto, Shinya
- Costain, Gregory
- Bellen, Hugo J.
2023
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Journal of clinical immunology, 2019-04, Vol.39 (3), p.249-256
2019
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Human mutation, 2019-05, Vol.40 (5), p.619-630
- Lenk, Guy M.
- Berry, Ian R.
- Stutterd, Chloe A.
- Blyth, Moira
- Green, Lydia
- Vadlamani, Gayatri
- Warren, Daniel
- Craven, Ian
- Fanjul‐Fernandez, Miriam
- Rodriguez‐Casero, Victoria
- Lockhart, Paul J.
- Vanderver, Adeline
- Simons, Cas
- Gibb, Susan
- Sadedin, Simon
- White, Susan M.
- Christodoulou, John
- Skibina, Olga
- Ruddle, Jonathan
- Tan, Tiong Y.
- Leventer, Richard J.
- Livingston, John H.
- Meisler, Miriam H.
2019
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European journal of medical genetics, 2015-01, Vol.58 (1), p.44-46
2015
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European journal of medical genetics, 2019-01, Vol.62 (1), p.27-34
2019
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Clinical dysmorphology, 2011-04, Vol.20 (2), p.73-74
2011
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Human mutation, 2019-05, Vol.40 (5), p.619-630
- Lenk, Guy M.
- Berry, Ian R.
- Stutterd, Chloe A.
- Blyth, Moira
- Green, Lydia
- Vadlamani, Gayatri
- Warren, Daniel
- Craven, Ian
- Fanjul-Fernandez, Miriam
- Rodriguez-Casero, Victoria
- Lockhart, Paul J.
- Vanderver, Adeline
- Simons, Cas
- Gibb, Susan
- Sadedin, Simon
- White, Susan M.
- Christodoulou, John
- Skibina, Olga
- Ruddle, Jonathan
- Tan, Tiong Y.
- Leventer, Richard J.
- Livingston, John H.
- Meisler, Miriam H.
2019
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Wellcome open research, 2018, Vol.3, p.46-46
- Tatton-Brown, Katrina
- Zachariou, Anna
- Loveday, Chey
- Renwick, Anthony
- Mahamdallie, Shazia
- Aksglaede, Lise
- Baralle, Diana
- Barge-Schaapveld, Daniela
- Blyth, Moira
- Bouma, Mieke
- Breckpot, Jeroen
- Crabb, Beau
- Dabir, Tabib
- Cormier-Daire, Valerie
- Fauth, Christine
- Fisher, Richard
- Gener, Blanca
- Goudie, David
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- Hunter, Matthew
- Jorgensen, Agnete
- Kant, Sarina G
- Kirally-Borri, Cathy
- Koolen, David
- Kumar, Ajith
- Labilloy, Anatalia
- Lees, Melissa
- Marcelis, Carlo
- Mercer, Catherine
- Mignot, Cyril
- Miller, Kathryn
- Neas, Katherine
- Newbury-Ecob, Ruth
- Pilz, Daniela T
- Posmyk, Renata
- Prada, Carlos
- Ramsey, Keri
- Randolph, Linda M
- Selicorni, Angelo
- Shears, Deborah
- Suri, Mohnish
- Temple, I Karen
- Turnpenny, Peter
- Val Maldergem, Lionel
- Varghese, Vinod
- Veenstra-Knol, Hermine E
- Yachelevich, Naomi
- Yates, Laura
- Rahman, Nazneen
2018
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American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2764-2768
2014
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American journal of medical genetics. Part A, 2016-05, Vol.170A (5), p.1115-1126
- Tooley, Madeleine
- Lynch, Danielle
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- Calder, Alistair
- Itasaki, Nobue
- Wakeling, Emma
- Scott, Richard
- Lees, Melissa
- Clayton-Smith, Jill
- Blyth, Moira
- Morton, Jenny
- Shears, Debbie
- Kini, Usha
- Homfray, Tessa
- Clarke, Angus
- Barnicoat, Angela
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- Offiah, Amaka
- Saunders, Michael
- Langton-Hewer, Simon
- Hilliard, Tom
- Davis, Peter
- Smithson, Sarah
2016
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Clinical dysmorphology, 2010-04, Vol.19 (2), p.62-64
2010
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Clinical dysmorphology, 2017-04, Vol.26 (2), p.101-106
2017
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Nature communications, 2019-02, Vol.10 (1), p.883-4, Article 883
- Blok, Lot Snijders
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2019
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Clinical dysmorphology, 2014-04, Vol.23 (2), p.56-59
2014
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Clinical dysmorphology, 2016-10, Vol.25 (4), p.135-145
2016
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