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Wyszukujesz frazę ""Willing, Marcia"" wg kryterium: Autor


Tytuł :
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior
Autorzy :
Harris, Holly K.Aff1, Aff2
Nakayama, TojoAff3, Aff4
Lai, JennyAff3, Aff5
Zhao, BoxunAff3, Aff4
Argyrou, NikoletaAff3, Aff4
Gubbels, Cynthia S.Aff3, Aff4
Soucy, AubrieAff3, Aff4
Genetti, Casie A.Aff3, Aff4
Suslovitch, VictoriaAff3, Aff4
Rodan, Lance H.Aff3, Aff4, Aff6
Tiller, George E.
Lesca, Gaetan
Gripp, Karen W.
Asadollahi, Reza
Hamosh, Ada
Applegate, Carolyn D.
Turnpenny, Peter D.
Simon, Marleen E. H.
Volker-Touw, Catharina M. L.
Gassen, Koen L. I. van
Binsbergen, Ellen van
Pfundt, Rolph
Gardeitchik, Thatjana
Vries, Bert B. A. de
Immken, LaDonna L.
Buchanan, Catherine
Willing, Marcia
Toler, Tomi L.
Fassi, Emily
Baker, Laura
Vansenne, Fleur
Wang, Xiadong
Ambrus, Jr., Julian L.
Fannemel, Madeleine
Posey, Jennifer E.
Agolini, Emanuele
Novelli, Antonio
Rauch, Anita
Boonsawat, Paranchai
Fagerberg, Christina R.
Larsen, Martin J.
Kibaek, Maria
Labalme, Audrey
Poisson, Alice
Payne, Katelyn K.
Walsh, Laurence E.Aff24, Aff25
Aldinger, Kimberly A.
Balciuniene, Jorune
Skraban, Cara
Gray, Christopher
Murrell, Jill
Bupp, Caleb P.
Pascolini, Giulia
Grammatico, Paola
Broly, Martin
Küry, Sébastien
Nizon, Mathilde
Rasool, Iqra GhulamAff31, Aff32
Zahoor, Muhammad Yasir
Kraus, Cornelia
Reis, André
Iqbal, Muhammad
Uguen, KevinAff34, Aff35
Audebert-Bellanger, Severine
Ferec, ClaudeAff34, Aff35
Redon, SylviaAff34, Aff35
Baker, Janice
Wu, Yunhong
Zampino, Guiseppe
Syrbe, Steffan
Brosse, Ines
Jamra, Rami Abou
Dobyns, William B.
Cohen, Lilian L.
Blomhoff, Anne
Mignot, CyrilAff43, Aff44
Keren, Boris
Courtin, Thomas
Agrawal, Pankaj B.Aff3, Aff4
Beggs, Alan H.Aff3, Aff4
Yu, Timothy W.Aff3, Aff4, Aff5
Pokaż więcej
Źródło :
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 23(6):1028-1040
Czasopismo naukowe
Tytuł :
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Autorzy :
Hengel, HolgerAff1, Aff2
Bosso-Lefèvre, CéliaAff3, Aff4
Grady, George
Szenker-Ravi, Emmanuelle
Li, Hankun
Pierce, Sarah
Lebigot, Élise
Tan, Thong-Teck
Eio, Michelle Y.
Narayanan, Gunaseelan
Utami, Kagistia Hana
Yau, Monica
Handal, Nader
Deigendesch, Werner
Keimer, Reinhard
Marzouqa, Hiyam M.
Gunay-Aygun, Meral
Muriello, Michael J.
Verhelst, Helene
Weckhuysen, SarahAff16, Aff17, Aff18
Mahida, Sonal
Naidu, Sakkubai
Thomas, Terrence G.
Lim, Jiin YingAff21, Aff22, Aff23
Tan, Ee ShienAff21, Aff22, Aff23
Haye, Damien
Willemsen, Michèl A. A. P.
Oegema, Renske
Mitchell, Wendy G.
Pierson, Tyler Mark
Andrews, Marisa V.
Willing, Marcia C.
Rodan, Lance H.
Barakat, Tahsin Stefan
van Slegtenhorst, Marjon
Gavrilova, Ralitza H.
Martinelli, Diego
Gilboa, Tal
Tamim, Abdullah M.
Hashem, Mais O.
AlSayed, Moeenaldeen D.
Abdulrahim, Maha M.
Al-Owain, Mohammed
Awaji, Ali
Mahmoud, Adel A. H.
Faqeih, Eissa A.
Asmari, Ali Al
Algain, Sulwan M.
Jad, Lamyaa A.
Aldhalaan, Hesham M.
Helbig, Ingo
Koolen, David A.
Riess, Angelika
Kraegeloh-Mann, Ingeborg
Bauer, Peter
Gulsuner, Suleyman
Stamberger, HannahAff16, Aff17, Aff18
Ng, Alvin Yu Jin
Tang, Sha
Tohari, Sumanty
Keren, Boris
Schultz-Rogers, Laura E.
Klee, Eric W.
Barresi, Sabina
Tartaglia, Marco
Mor-Shaked, Hagar
Maddirevula, Sateesh
Begtrup, Amber
Telegrafi, Aida
Pfundt, Rolph
Schüle, RebeccaAff1, Aff2
Ciruna, Brian
Bonnard, Carine
Pouladi, Mahmoud A.Aff10, Aff52, Aff53
Stewart, James C.
Claridge-Chang, AdamAff47, Aff54
Lefeber, Dirk J.Aff55, Aff56
Alkuraya, Fowzan S.
Mathuru, Ajay S.Aff6, Aff47
Venkatesh, ByrappaAff4, Aff47
Barycki, Joseph J.
Simpson, Melanie A.
Jamuar, Saumya S.Aff21, Aff22, Aff23, Aff57
Schöls, LudgerAff1, Aff2
Reversade, BrunoAff3, Aff4, Aff47, Aff58, Aff59
Pokaż więcej
Źródło :
Nature Communications. 11(1)
Czasopismo naukowe
Tytuł :
Biallelic ASCC1 variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (SMABF2).
Autorzy :
Rosano, Kristen K.
Wegner, Daniel J.
Shinawi, Marwan
Baldridge, Dustin
Bucelli, Robert C.
Dahiya, Sonika
White, Frances V.
Willing, Marcia C.
McAllister, William
Taft, Ryan J.
Bluske, Krista
Buchanan, Amanda
Cole, Francis Sessions
Wambach, Jennifer A.
Pokaż więcej
Źródło :
American Journal of Medical Genetics. Part A; Jul2021, Vol. 185 Issue 7, p2190-2197, 8p
Czasopismo naukowe
Tytuł :
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Autorzy :
Snijders Blok, LotAff1, Aff2, Aff3
Rousseau, Justine
Twist, Joanna
Ehresmann, Sophie
Takaku, Motoki
Venselaar, Hanka
Rodan, Lance H.
Nowak, Catherine B.
Douglas, Jessica
Swoboda, Kathryn J.
Steeves, Marcie A.
Sahai, Inderneel
Stumpel, Connie T. R. M.
Stegmann, Alexander P. A.
Wheeler, Patricia
Willing, Marcia
Fiala, Elise
Kochhar, Aaina
Gibson, William T.Aff14, Aff15
Cohen, Ana S. A.Aff14, Aff15
Agbahovbe, RukyAff14, Aff15
Innes, A. Micheil
Au, P. Y. Billie
Rankin, Julia
Anderson, Ilse J.
Skinner, Steven A.
Louie, Raymond J.
Warren, Hannah E.
Afenjar, Alexandra
Keren, BorisAff21, Aff22
Nava, CarolineAff21, Aff22, Aff23
Buratti, Julien
Isapof, Arnaud
Rodriguez, Diana
Lewandowski, Raymond
Propst, Jennifer
van Essen, Ton
Choi, Murim
Lee, Sangmoon
Chae, Jong H.
Price, Susan
Schnur, Rhonda E.
Douglas, Ganka
Wentzensen, Ingrid M.
Zweier, Christiane
Reis, André
Bialer, Martin G.
Moore, Christine
Koopmans, Marije
Brilstra, Eva H.
Monroe, Glen R.
van Gassen, Koen L. I.
van Binsbergen, Ellen
Newbury-Ecob, Ruth
Bownass, Lucy
Bader, Ingrid
Mayr, Johannes A.
Wortmann, Saskia B.Aff37, Aff38, Aff39
Jakielski, Kathy J.
Strand, Edythe A.
Kloth, Katja
Bierhals, Tatjana
The DDD study
Roberts, John D.
Petrovich, Robert M.
Machida, Shinichi
Kurumizaka, Hitoshi
Lelieveld, Stefan
Pfundt, Rolph
Jansen, SandraAff1, Aff3
Deriziotis, Pelagia
Faivre, LaurenceAff44, Aff45
Thevenon, JulienAff44, Aff45
Assoum, MirnaAff44, Aff45
Shriberg, Lawrence
Kleefstra, TjitskeAff1, Aff3
Brunner, Han G.Aff1, Aff3, Aff10
Wade, Paul A.
Fisher, Simon E.Aff2, Aff3
Campeau, Philippe M.Aff4, Aff47
Pokaż więcej
Źródło :
Nature Communications. 10(1)
Czasopismo naukowe
Tytuł :
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Autorzy :
Blok, Lot SnijdersAff1, Aff2, Aff3
Rousseau, Justine
Twist, Joanna
Ehresmann, Sophie
Takaku, Motoki
Venselaar, Hanka
Rodan, Lance H.
Nowak, Catherine B.
Douglas, Jessica
Swoboda, Kathryn J.
Steeves, Marcie A.
Sahai, Inderneel
Stumpel, Connie T. R. M.
Stegmann, Alexander P. A.
Wheeler, Patricia
Willing, Marcia
Fiala, Elise
Kochhar, Aaina
Gibson, William T.Aff14, Aff15
Cohen, Ana S. A.Aff14, Aff15
Agbahovbe, RukyAff14, Aff15
Innes, A. Micheil
Au, P. Y. Billie
Rankin, Julia
Anderson, Ilse J.
Skinner, Steven A.
Louie, Raymond J.
Warren, Hannah E.
Afenjar, Alexandra
Keren, BorisAff21, Aff22
Nava, CarolineAff21, Aff22, Aff23
Buratti, Julien
Isapof, Arnaud
Rodriguez, Diana
Lewandowski, Raymond
Propst, Jennifer
van Essen, Ton
Choi, Murim
Lee, Sangmoon
Chae, Jong H.
Price, Susan
Schnur, Rhonda E.
Douglas, Ganka
Wentzensen, Ingrid M.
Zweier, Christiane
Reis, André
Bialer, Martin G.
Moore, Christine
Koopmans, Marije
Brilstra, Eva H.
Monroe, Glen R.
van Gassen, Koen L. I.
van Binsbergen, Ellen
Newbury-Ecob, Ruth
Bownass, Lucy
Bader, Ingrid
Mayr, Johannes A.
Wortmann, Saskia B.Aff37, Aff38, Aff39
Jakielski, Kathy J.
Strand, Edythe A.
Kloth, Katja
Bierhals, Tatjana
The DDD study
Roberts, John D.
Petrovich, Robert M.
Machida, Shinichi
Kurumizaka, Hitoshi
Lelieveld, Stefan
Pfundt, Rolph
Jansen, SandraAff1, Aff3
Deriziotis, Pelagia
Faivre, LaurenceAff44, Aff45
Thevenon, JulienAff44, Aff45
Assoum, MirnaAff44, Aff45
Shriberg, Lawrence
Kleefstra, TjitskeAff1, Aff3
Brunner, Han G.Aff1, Aff3, Aff10
Wade, Paul A.
Fisher, Simon E.Aff2, Aff3
Campeau, Philippe M.Aff4, Aff47
Pokaż więcej
Źródło :
Nature Communications. 10(1)
Czasopismo naukowe
Tytuł :
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Autorzy :
Snijders Blok, LotAff1, Aff2, Aff3
Rousseau, Justine
Twist, Joanna
Ehresmann, Sophie
Takaku, Motoki
Venselaar, Hanka
Rodan, Lance H.
Nowak, Catherine B.
Douglas, Jessica
Swoboda, Kathryn J.
Steeves, Marcie A.
Sahai, Inderneel
Stumpel, Connie T. R. M.
Stegmann, Alexander P. A.
Wheeler, Patricia
Willing, Marcia
Fiala, Elise
Kochhar, Aaina
Gibson, William T.Aff14, Aff15
Cohen, Ana S. A.Aff14, Aff15
Agbahovbe, RukyAff14, Aff15
Innes, A. Micheil
Au, P. Y. Billie
Rankin, Julia
Anderson, Ilse J.
Skinner, Steven A.
Louie, Raymond J.
Warren, Hannah E.
Afenjar, Alexandra
Keren, BorisAff21, Aff22
Nava, CarolineAff21, Aff22, Aff23
Buratti, Julien
Isapof, Arnaud
Rodriguez, Diana
Lewandowski, Raymond
Propst, Jennifer
van Essen, Ton
Choi, Murim
Lee, Sangmoon
Chae, Jong H.
Price, Susan
Schnur, Rhonda E.
Douglas, Ganka
Wentzensen, Ingrid M.
Zweier, Christiane
Reis, André
Bialer, Martin G.
Moore, Christine
Koopmans, Marije
Brilstra, Eva H.
Monroe, Glen R.
van Gassen, Koen L. I.
van Binsbergen, Ellen
Newbury-Ecob, Ruth
Bownass, Lucy
Bader, Ingrid
Mayr, Johannes A.
Wortmann, Saskia B.Aff37, Aff38, Aff39
Jakielski, Kathy J.
Strand, Edythe A.
Kloth, Katja
Bierhals, Tatjana
The DDD study
Roberts, John D.
Petrovich, Robert M.
Machida, Shinichi
Kurumizaka, Hitoshi
Lelieveld, Stefan
Pfundt, Rolph
Jansen, SandraAff1, Aff3
Deriziotis, Pelagia
Faivre, LaurenceAff44, Aff45
Thevenon, JulienAff44, Aff45
Assoum, MirnaAff44, Aff45
Shriberg, Lawrence
Kleefstra, TjitskeAff1, Aff3
Brunner, Han G.Aff1, Aff3, Aff10
Wade, Paul A.
Fisher, Simon E.Aff2, Aff3
Campeau, Philippe M.Aff4, Aff47
Pokaż więcej
Źródło :
Nature Communications. 9(1)
Czasopismo naukowe
Tytuł :
Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency
Autorzy :
Zawerton, Ash
Mignot, Cyril
Sigafoos, Ashley
Blackburn, Patrick
Haseeb, Abdul
McWalter, Kirsty
Ichikawa, Shoji
Nava, Caroline
Keren, Boris
Charles, Perrine
Marey, Isabelle
Tabet, Anne-Claude
Levy, Jonathan
Perrin, Laurence
Hartmann, Andreas
Lesca, Gaetan
Schluth-Bolard, Caroline
Monin, Pauline
Dupuis-Girod, Sophie
Guillen Sacoto, Maria
Schnur, Rhonda
Zhu, Zehua
POISSON, Alice
El Chehadeh, Salima
Alembik, Yves
Bruel, Ange-Line
Lehalle, Daphne
Nambot, Sophie
Moutton, Sébastien
Odent, Sylvie
Jaillard, Sylvie
Dubourg, Christèle
Hilhorst-Hofstee, Yvonne
Barbaro-Dieber, Tina
Ortega, Lucia
Bhoj, Elizabeth
Masser-Frye, Diane
Bird, Lynne
Lindstrom, Kristin
Ramsey, Keri
Narayanan, Vinodh
Fassi, Emily
Willing, Marcia
Cole, Trevor
Salter, Claire
Akilapa, Rhoda
Vandersteen, Anthony
Canham, Natalie
Rump, Patrick
Gerkes, Erica
Klein Wassink-Ruiter, Jolien
Bijlsma, Emilia
Hoffer, Mariëtte
Vargas, Marcelo
Wojcik, Antonina
Cherik, Florian
Francannet, Christine
Rosenfeld, Jill
Machol, Keren
Scott, Daryl
Bacino, Carlos
Wang, Xia
Clark, Gary
Bertoli, Marta
Zwolinski, Simon
Thomas, Rhys
Akay, Ela
Chang, Richard
Bressi, Rebekah
Sanchez Russo, Rossana
Srour, Myriam
Russell, Laura
Goyette, Anne-Marie
Dupuis, Lucie
Mendoza-Londono, Roberto
Karimov, Catherine
Joseph, Maries
Nizon, Mathilde
Cogné, Benjamin
Kuechler, Alma
Piton, Amélie
Klee, Eric
Lefebvre, Véronique
Clark, Karl
Depienne, Christel
Pokaż więcej
Temat :
epilepsy
developmental delay
[SDV.GEN]Life Sciences [q-bio]/Genetics
autism
missense variants
intellectual disability
Źródło :
Genetics in Medicine, Nature Publishing Group, 2020, 22 (3), pp.524-537. ⟨10.1038/s41436-019-0657-0⟩
Tytuł :
Effects of enamel matrix genes on dental caries are moderated by fluoride exposures
Autorzy :
Shaffer, John R.
Carlson, Jenna C.
Stanley, Brooklyn O. C.
Feingold, Eleanor
Cooper, Margaret
Vanyukov, Michael M.
Maher, Brion S.
Slayton, Rebecca L.
Willing, Marcia C.
Reis, Steven E.
McNeil, Daniel W.
Crout, Richard J.
Weyant, Robert J.
Levy, Steven M.
Vieira, Alexandre R.
Marazita, Mary L.
Pokaż więcej
Źródło :
Human Genetics. February 2015 134(2):159-167
Czasopismo naukowe
Tytuł :
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)
Autorzy :
Blok, Lot Snijders
Rousseau, Justine
Twist, Joanna
Ehresmann, Sophie
Takaku, Motoki
Venselaar, Hanka
Rodan, Lance H
Nowak, Catherine B
Douglas, Jessica
Swoboda, Kathryn J
Steeves, Marcie A
Sahai, Inderneel
Stumpel, Connie TRM
Stegmann, Alexander PA
Wheeler, Patricia
Willing, Marcia
Fiala, Elise
Kochhar, Aaina
Gibson, William T
Cohen, Ana SA
Agbahovbe, Ruky
Innes, A Micheil
Au, PY Billie
Rankin, Julia
Anderson, Ilse J
Skinner, Steven A
Louie, Raymond J
Warren, Hannah E
Afenjar, Alexandra
Keren, Boris
Nava, Caroline
Buratti, Julien
Isapof, Arnaud
Rodriguez, Diana
Lewandowski, Raymond
Propst, Jennifer
van Essen, Ton
Choi, Murim
Lee, Sangmoon
Chae, Jong H
Price, Susan
Schnur, Rhonda E
Douglas, Ganka
Wentzensen, Ingrid M
Zweier, Christiane
Reis, Andre
Bialer, Martin G
Moore, Christine
Koopmans, Marije
Brilstra, Eva H
Monroe, Glen R
van Gassen, Koen LI
van Binsbergen, Ellen
Newbury-Ecob, Ruth
Bownass, Lucy
Bader, Ingrid
Mayr, Johannes A
Wortmann, Saskia B
Jakielski, Kathy J
Strand, Edythe A
Kloth, Katja
Bierhals, Tatjana
Roberts, John D
Petrovich, Robert M
Machida, Shinichi
Kurumizaka, Hitoshi
Lelieveld, Stefan
Pfundt, Rolph
Jansen, Sandra
Deriziotis, Pelagia
Faivre, Laurence
Thevenon, Julien
Assoum, Mirna
Shriberg, Lawrence
Kleefstra, Tjitske
Brunner, Han G
Wade, Paul A
Fisher, Simon E
Campeau, Philippe M
McRae, Jeremy F
Clayton, Stephen
Fitzgerald, Tomas W
Kaplanis, Joanna
Prigmore, Elena
Rajan, Diana
Sifrim, Alejandro
Aitken, Stuart
Akawi, Nadia
Alvi, Mohsan
Ambridge, Kirsty
Barrett, Daniel M
Bayzetinova, Tanya
Jones, Philip
Jones, Wendy D
King, Daniel
Krishnappa, Netravathi
Mason, Laura E
Singh, Tarjinder
Tivey, Adrian R
Ahmed, Munaza
Anjum, Uruj
Archer, Hayley
Armstrong, Ruth
Awada, Jana
Balasubramanian, Meena
Banka, Siddharth
Baralle, Diana
Barnicoat, Angela
Batstone, Paul
Baty, David
Bennett, Chris
Berg, Jonathan
Bernhard, Birgitta
Bevan, A Paul
Bitner-Glindzicz, Maria
Blair, Edward
Blyth, Moira
Bohanna, David
Bourdon, Louise
Bourn, David
Bradley, Lisa
Brady, Angela
Brent, Simon
Brewer, Carole
Brunstrom, Kate
Bunyan, David J
Burn, John
Canham, Natalie
Castle, Bruce
Chandler, Kate
Chatzimichali, Elena
Cilliers, Deirdre
Clarke, Angus
Clasper, Susan
Clayton-Smith, Jill
Clowes, Virginia
Coates, Andrea
Cole, Trevor
Colgiu, Irina
Collins, Amanda
Collinson, Morag N
Connell, Fiona
Cooper, Nicola
Cox, Helen
Cresswell, Lara
Cross, Gareth
Crow, Yanick
D'Alessandro, Mariella
Dabir, Tabib
Davidson, Rosemarie
Davies, Sally
de Vries, Dylan
Dean, John
Deshpande, Charu
Devlin, Gemma
Dixit, Abhijit
Dobbie, Angus
Donaldson, Alan
Donnai, Dian
Donnelly, Deirdre
Donnelly, Carina
Douglas, Angela
Douzgou, Sofia
Duncan, Alexis
Eason, Jacqueline
Ellard, Sian
Ellis, Ian
Elmslie, Frances
Evans, Karenza
Everest, Sarah
Fendick, Tina
Fisher, Richard
Flinter, Frances
Foulds, Nicola
Fry, Andrew
Fryer, Alan
Gardiner, Carol
Gaunt, Lorraine
Ghali, Neeti
Gibbons, Richard
Gill, Harinder
Goodship, Judith
Goudie, David
Gray, Emma
Green, Andrew
Greene, Philip
Greenhalgh, Lynn
Gribble, Susan
Harrison, Rachel
Harrison, Lucy
Harrison, Victoria
Hawkins, Rose
He, Liu
Hellens, Stephen
Henderson, Alex
Hewitt, Sarah
Hildyard, Lucy
Hobson, Emma
Holden, Simon
Holder, Muriel
Holder, Susan
Hollingsworth, Georgina
Homfray, Tessa
Humphreys, Mervyn
Hurst, Jane
Hutton, Ben
Ingram, Stuart
Irving, Melita
Islam, Lily
Jackson, Andrew
Jarvis, Joanna
Jenkins, Lucy
Johnson, Diana
Jones, Elizabeth
Josifova, Dragana
Joss, Shelagh
Kaemba, Beckie
Kazembe, Sandra
Kelsell, Rosemary
Kerr, Bronwyn
Kingston, Helen
Kini, Usha
Kinning, Esther
Kirby, Gail
Kirk, Claire
Kivuva, Emma
Kraus, Alison
Kumar, Dhavendra
Kumar, VK Ajith
Lachlan, Katherine
Lam, Wayne
Lampe, Anne
Langman, Caroline
Lees, Melissa
Lim, Derek
Longman, Cheryl
Lowther, Gordon
Lynch, Sally A
Magee, Alex
Maher, Eddy
Male, Alison
Mansour, Sahar
Marks, Karen
Martin, Katherine
Maye, Una
McCann, Emma
McConnell, Vivienne
McEntagart, Meriel
McGowan, Ruth
McKay, Kirsten
McKee, Shane
McMullan, Dominic J
McNerlan, Susan
McWilliam, Catherine
Mehta, Sarju
Metcalfe, Kay
Middleton, Anna
Miedzybrodzka, Zosia
Miles, Emma
Mohammed, Shehla
Montgomery, Tara
Moore, David
Morgan, Sian
Morton, Jenny
Mugalaasi, Hood
Murday, Victoria
Murphy, Helen
Naik, Swati
Nemeth, Andrea
Nevitt, Louise
Norman, Andrew
O'Shea, Rosie
Ogilvie, Caroline
Ong, Kai-Ren
Park, Soo-Mi
Parker, Michael J
Patel, Chirag
Paterson, Joan
Payne, Stewart
Perrett, Daniel
Phipps, Julie
Pilz, Daniela T
Pollard, Martin
Pottinger, Caroline
Poulton, Joanna
Pratt, Norman
Prescott, Katrina
Pridham, Abigail
Procter, Annie
Purnell, Hellen
Quarrell, Oliver
Ragge, Nicola
Rahbari, Raheleh
Randall, Josh
Raymond, Lucy
Rice, Debbie
Robert, Leema
Roberts, Eileen
Roberts, Jonathan
Roberts, Paul
Roberts, Gillian
Ross, Alison
Rosser, Elisabeth
Saggar, Anand
Samant, Shalaka
Sampson, Julian
Sandford, Richard
Sarkar, Ajoy
Schweiger, Susann
Scott, Richard
Scurr, Ingrid
Selby, Ann
Seller, Anneke
Sequeira, Cheryl
Shannon, Nora
Sharif, Saba
Shaw-Smith, Charles
Shearing, Emma
Shears, Debbie
Sheridan, Eamonn
Simonic, Ingrid
Singzon, Roldan
Skitt, Zara
Smith, Audrey
Smith, Kath
Smithson, Sarah
Sneddon, Linda
Splitt, Miranda
Squires, Miranda
Stewart, Fiona
Stewart, Helen
Straub, Volker
Suri, Mohnish
Sutton, Vivienne
Swaminathan, Ganesh Jawahar
Sweeney, Elizabeth
Tatton-Brown, Kate
Taylor, Cat
Taylor, Rohan
Tein, Mark
Temple, I Karen
Thomson, Jenny
Tischkowitz, Marc
Tomkins, Susan
Torokwa, Audrey
Treacy, Becky
Turner, Claire
Turnpenny, Peter
Tysoe, Carolyn
Vandersteen, Anthony
Varghese, Vinod
Vasudevan, Pradeep
Vijayarangakannan, Parthiban
Vogt, Julie
Wakeling, Emma
Wallwark, Sarah
Waters, Jonathon
Weber, Astrid
Wellesley, Diana
Whiteford, Margo
Widaa, Sara
Wilcox, Sarah
Wilkinson, Emily
Williams, Denise
Williams, Nicola
Wilson, Louise
Woods, Geoff
Wragg, Christopher
Wright, Michael
Yates, Laura
Yau, Michael
Nellaker, Chris
Parker, Michael
Firth, Helen V
Wright, Caroline F
FitzPatrick, David R
Barrett, Jeffrey C
Hurles, Matthew E
Study, DDD
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