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Further delineation of Kabuki syndrome in 48 well-defined new individuals. [electronic resource] by
- Armstrong, Linlea
- Abd El Moneim, Azza
- Aleck, Kirk
- Aughton, David J
- Baumann, Clarisse
- Braddock, Stephen R
- Gillessen-Kaesbach, Gabriele
- Graham, John M
- Grebe, Theresa A
- Gripp, Karen W
- Hall, Bryan D
- Hennekam, Raoul
- Hunter, Alasdair
- Keppler-Noreuil, Kim
- Lacombe, Didier
- Lin, Angela E
- Ming, Jeffrey E
- Kokitsu-Nakata, Nancy Mizue
- Nikkel, Sarah M
- Philip, Nicole
- Raas-Rothschild, Annick
- Sommer, Annemarie
- Verloes, Alain
- Walter, Claudia
- Wieczorek, Dagmar
- Williams, Marc S
- Zackai, Elaine
- Allanson, Judith E
Producer: 20050315
In:
American journal of medical genetics. Part A vol. 132A
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102.
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Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder. [electronic resource] by
- Mullegama, Sureni V
- Rosenfeld, Jill A
- Orellana, Carmen
- van Bon, Bregje W M
- Halbach, Sara
- Repnikova, Elena A
- Brick, Lauren
- Li, Chumei
- Dupuis, Lucie
- Rosello, Monica
- Aradhya, Swaroop
- Stavropoulos, D James
- Manickam, Kandamurugu
- Mitchell, Elyse
- Hodge, Jennelle C
- Talkowski, Michael E
- Gusella, James F
- Keller, Kory
- Zonana, Jonathan
- Schwartz, Stuart
- Pyatt, Robert E
- Waggoner, Darrel J
- Shaffer, Lisa G
- Lin, Angela E
- de Vries, Bert B A
- Mendoza-Londono, Roberto
- Elsea, Sarah H
Producer: 20150212
In:
European journal of human genetics : EJHG vol. 22
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103.
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Myhre and LAPS syndromes: clinical and molecular review of 32 patients. [electronic resource] by
- Michot, Caroline
- Le Goff, Carine
- Mahaut, Clémentine
- Afenjar, Alexandra
- Brooks, Alice S
- Campeau, Philippe M
- Destree, Anne
- Di Rocco, Maja
- Donnai, Dian
- Hennekam, Raoul
- Heron, Delphine
- Jacquemont, Sébastien
- Kannu, Peter
- Lin, Angela E
- Manouvrier-Hanu, Sylvie
- Mansour, Sahar
- Marlin, Sandrine
- McGowan, Ruth
- Murphy, Helen
- Raas-Rothschild, Annick
- Rio, Marlène
- Simon, Marleen
- Stolte-Dijkstra, Irene
- Stone, James R
- Sznajer, Yves
- Tolmie, John
- Touraine, Renaud
- van den Ende, Jenneke
- Van der Aa, Nathalie
- van Essen, Ton
- Verloes, Alain
- Munnich, Arnold
- Cormier-Daire, Valérie
Producer: 20150625
In:
European journal of human genetics : EJHG vol. 22
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Genotype-phenotype analysis of the branchio-oculo-facial syndrome. [electronic resource] by
- Milunsky, Jeff M
- Maher, Tom M
- Zhao, Geping
- Wang, Zhenyuan
- Mulliken, John B
- Chitayat, David
- Clemens, Michele
- Stalker, Heather J
- Bauer, Mislen
- Burch, Michele
- Chénier, Sébastien
- Cunningham, Michael L
- Drack, Arlene V
- Janssens, Sandra
- Karlea, Audrey
- Klatt, Regan
- Kini, Usha
- Klein, Ophir
- Lachmeijer, Augusta M
- Megarbane, Andre
- Mendelsohn, Nancy J
- Meschino, Wendy S
- Mortier, Geert R
- Parkash, Sandhya
- Ray, C Renai
- Roberts, Angharad
- Roberts, Amy
- Reardon, Willie
- Schnur, Rhonda E
- Smith, Rosemarie
- Splitt, Miranda
- Tezcan, Kamer
- Whiteford, Margo L
- Wong, Derek A
- Zori, Roberto
- Lin, Angela E
Producer: 20110517
In:
American journal of medical genetics. Part A vol. 155A
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105.
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Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. [electronic resource] by
- Fischer-Zirnsak, Björn
- Escande-Beillard, Nathalie
- Ganesh, Jaya
- Tan, Yu Xuan
- Al Bughaili, Mohammed
- Lin, Angela E
- Sahai, Inderneel
- Bahena, Paulina
- Reichert, Sara L
- Loh, Abigail
- Wright, Graham D
- Liu, Jaron
- Rahikkala, Elisa
- Pivnick, Eniko K
- Choudhri, Asim F
- Krüger, Ulrike
- Zemojtel, Tomasz
- van Ravenswaaij-Arts, Conny
- Mostafavi, Roya
- Stolte-Dijkstra, Irene
- Symoens, Sofie
- Pajunen, Leila
- Al-Gazali, Lihadh
- Meierhofer, David
- Robinson, Peter N
- Mundlos, Stefan
- Villarroel, Camilo E
- Byers, Peter
- Masri, Amira
- Robertson, Stephen P
- Schwarze, Ulrike
- Callewaert, Bert
- Reversade, Bruno
- Kornak, Uwe
Producer: 20151208
In:
American journal of human genetics vol. 97
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106.
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Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back. [electronic resource] by
- Rauen, Katherine A
- Schoyer, Lisa
- McCormick, Frank
- Lin, Angela E
- Allanson, Judith E
- Stevenson, David A
- Gripp, Karen W
- Neri, Giovanni
- Carey, John C
- Legius, Eric
- Tartaglia, Marco
- Schubbert, Suzanne
- Roberts, Amy E
- Gelb, Bruce D
- Shannon, Kevin
- Gutmann, David H
- McMahon, Martin
- Guerra, Carmen
- Fagin, James A
- Yu, Benjamin
- Aoki, Yoko
- Neel, Benjamin G
- Balmain, Allan
- Drake, Richard R
- Nolan, Garry P
- Zenker, Martin
- Bollag, Gideon
- Sebolt-Leopold, Judith
- Gibbs, Jackson B
- Silva, Alcino J
- Patton, E Elizabeth
- Viskochil, David H
- Kieran, Mark W
- Korf, Bruce R
- Hagerman, Randi J
- Packer, Roger J
- Melese, Teri
Producer: 20100405
In:
American journal of medical genetics. Part A vol. 152A
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107.
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Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy. [electronic resource] by
- Carvill, Gemma L
- Helbig, Katherine L
- Myers, Candace T
- Scala, Marcello
- Huether, Robert
- Lewis, Sara
- Kruer, Tyler N
- Guida, Brandon S
- Bakhtiari, Somayeh
- Sebe, Joy
- Tang, Sha
- Stickney, Heather
- Oktay, Sehribani Ulusoy
- Bhandiwad, Ashwin A
- Ramsey, Keri
- Narayanan, Vinodh
- Feyma, Timothy
- Rohena, Luis O
- Accogli, Andrea
- Severino, Mariasavina
- Hollingsworth, Georgina
- Gill, Deepak
- Depienne, Christel
- Nava, Caroline
- Sadleir, Lynette G
- Caruso, Paul A
- Lin, Angela E
- Jansen, Floor E
- Koeleman, Bobby
- Brilstra, Eva
- Willemsen, Marjolein H
- Kleefstra, Tjitske
- Sa, Joaquim
- Mathieu, Marie-Laure
- Perrin, Laurine
- Lesca, Gaetan
- Striano, Pasquale
- Casari, Giorgio
- Scheffer, Ingrid E
- Raible, David
- Sattlegger, Evelyn
- Capra, Valeria
- Padilla-Lopez, Sergio
- Mefford, Heather C
- Kruer, Michael C
Producer: 20211105
In:
Human mutation vol. 41
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108.
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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes. [electronic resource] by
- Rivière, Jean-Baptiste
- Mirzaa, Ghayda M
- O'Roak, Brian J
- Beddaoui, Margaret
- Alcantara, Diana
- Conway, Robert L
- St-Onge, Judith
- Schwartzentruber, Jeremy A
- Gripp, Karen W
- Nikkel, Sarah M
- Worthylake, Thea
- Sullivan, Christopher T
- Ward, Thomas R
- Butler, Hailly E
- Kramer, Nancy A
- Albrecht, Beate
- Armour, Christine M
- Armstrong, Linlea
- Caluseriu, Oana
- Cytrynbaum, Cheryl
- Drolet, Beth A
- Innes, A Micheil
- Lauzon, Julie L
- Lin, Angela E
- Mancini, Grazia M S
- Meschino, Wendy S
- Reggin, James D
- Saggar, Anand K
- Lerman-Sagie, Tally
- Uyanik, Gökhan
- Weksberg, Rosanna
- Zirn, Birgit
- Beaulieu, Chandree L
- Majewski, Jacek
- Bulman, Dennis E
- O'Driscoll, Mark
- Shendure, Jay
- Graham, John M
- Boycott, Kym M
- Dobyns, William B
Producer: 20121009
In:
Nature genetics vol. 44
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Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a Nose. [electronic resource] by
- Delaney, Angela
- Volochayev, Rita
- Meader, Brooke
- Lee, Janice
- Almpani, Konstantinia
- Noukelak, Germaine Y
- Henkind, Jennifer
- Chalmers, Laura
- Law, Jennifer R
- Williamson, Kathleen A
- Jacobsen, Christina M
- Buitrago, Tatiana Pineda
- Perez, Orlando
- Cho, Chie-Hee
- Kaindl, Angela
- Rauch, Anita
- Steindl, Katharina
- Garcia, Jose Elias
- Russell, Bianca E
- Prasad, Rameshwar
- Mondal, Uttam K
- Reigstad, Hallvard M
- Clements, Scott
- Kim, Susan
- Inoue, Kaoru
- Arora, Gazal
- Salnikov, Kathryn B
- DiOrio, Nicole P
- Prada, Rolando
- Capri, Yline
- Morioka, Kosuke
- Mizota, Michiyo
- Zechi-Ceide, Roseli M
- Kokitsu-Nakata, Nancy M
- Tonello, Cristiano
- Vendramini-Pittoli, Siulan
- da Silva Dalben, Gisele
- Balasubramanian, Ravikumar
- Dwyer, Andrew A
- Seminara, Stephanie B
- Crowley, William F
- Plummer, Lacey
- Hall, Janet E
- Graham, John M
- Lin, Angela E
- Shaw, Natalie D
Producer: 20210203
In:
The Journal of clinical endocrinology and metabolism vol. 105
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110.
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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. [electronic resource] by
- Johnston, Jennifer J
- Olivos-Glander, Isabelle
- Killoran, Christina
- Elson, Emma
- Turner, Joyce T
- Peters, Kathryn F
- Abbott, Margaret H
- Aughton, David J
- Aylsworth, Arthur S
- Bamshad, Michael J
- Booth, Carol
- Curry, Cynthia J
- David, Albert
- Dinulos, Mary Beth
- Flannery, David B
- Fox, Michelle A
- Graham, John M
- Grange, Dorothy K
- Guttmacher, Alan E
- Hannibal, Mark C
- Henn, Wolfram
- Hennekam, Raoul C M
- Holmes, Lewis B
- Hoyme, H Eugene
- Leppig, Kathleen A
- Lin, Angela E
- Macleod, Patrick
- Manchester, David K
- Marcelis, Carlo
- Mazzanti, Laura
- McCann, Emma
- McDonald, Marie T
- Mendelsohn, Nancy J
- Moeschler, John B
- Moghaddam, Billur
- Neri, Giovanni
- Newbury-Ecob, Ruth
- Pagon, Roberta A
- Phillips, John A
- Sadler, Laurie S
- Stoler, Joan M
- Tilstra, David
- Walsh Vockley, Catherine M
- Zackai, Elaine H
- Zadeh, Touran M
- Brueton, Louise
- Black, Graeme Charles M
- Biesecker, Leslie G
Producer: 20050516
In:
American journal of human genetics vol. 76
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111.
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Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations. [electronic resource] by
- Johnston, Jennifer J
- Sapp, Julie C
- Turner, Joyce T
- Amor, David
- Aftimos, Salim
- Aleck, Kyrieckos A
- Bocian, Maureen
- Bodurtha, Joann N
- Cox, Gerald F
- Curry, Cynthia J
- Day, Ruth
- Donnai, Dian
- Field, Michael
- Fujiwara, Ikuma
- Gabbett, Michael
- Gal, Moran
- Graham, John M
- Hedera, Peter
- Hennekam, Raoul C M
- Hersh, Joseph H
- Hopkin, Robert J
- Kayserili, Hülya
- Kidd, Alexa M J
- Kimonis, Virginia
- Lin, Angela E
- Lynch, Sally Ann
- Maisenbacher, Melissa
- Mansour, Sahar
- McGaughran, Julie
- Mehta, Lakshmi
- Murphy, Helen
- Raygada, Margarita
- Robin, Nathaniel H
- Rope, Alan F
- Rosenbaum, Kenneth N
- Schaefer, G Bradley
- Shealy, Amy
- Smith, Wendy
- Soller, Maria
- Sommer, Annmarie
- Stalker, Heather J
- Steiner, Bernhard
- Stephan, Mark J
- Tilstra, David
- Tomkins, Susan
- Trapane, Pamela
- Tsai, Anne Chun-Hui
- Van Allen, Margot I
- Vasudevan, Pradeep C
- Zabel, Bernhard
- Zunich, Janice
- Black, Graeme C M
- Biesecker, Leslie G
Producer: 20110128
In:
Human mutation vol. 31
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112.
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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [electronic resource] by
- Shaw, Natalie D
- Brand, Harrison
- Kupchinsky, Zachary A
- Bengani, Hemant
- Plummer, Lacey
- Jones, Takako I
- Erdin, Serkan
- Williamson, Kathleen A
- Rainger, Joe
- Stortchevoi, Alexei
- Samocha, Kaitlin
- Currall, Benjamin B
- Dunican, Donncha S
- Collins, Ryan L
- Willer, Jason R
- Lek, Angela
- Lek, Monkol
- Nassan, Malik
- Pereira, Shahrin
- Kammin, Tammy
- Lucente, Diane
- Silva, Alexandra
- Seabra, Catarina M
- Chiang, Colby
- An, Yu
- Ansari, Morad
- Rainger, Jacqueline K
- Joss, Shelagh
- Smith, Jill Clayton
- Lippincott, Margaret F
- Singh, Sylvia S
- Patel, Nirav
- Jing, Jenny W
- Law, Jennifer R
- Ferraro, Nalton
- Verloes, Alain
- Rauch, Anita
- Steindl, Katharina
- Zweier, Markus
- Scheer, Ianina
- Sato, Daisuke
- Okamoto, Nobuhiko
- Jacobsen, Christina
- Tryggestad, Jeanie
- Chernausek, Steven
- Schimmenti, Lisa A
- Brasseur, Benjamin
- Cesaretti, Claudia
- García-Ortiz, Jose E
- Buitrago, Tatiana Pineda
- Silva, Orlando Perez
- Hoffman, Jodi D
- Mühlbauer, Wolfgang
- Ruprecht, Klaus W
- Loeys, Bart L
- Shino, Masato
- Kaindl, Angela M
- Cho, Chie-Hee
- Morton, Cynthia C
- Meehan, Richard R
- van Heyningen, Veronica
- Liao, Eric C
- Balasubramanian, Ravikumar
- Hall, Janet E
- Seminara, Stephanie B
- Macarthur, Daniel
- Moore, Steven A
- Yoshiura, Koh-Ichiro
- Gusella, James F
- Marsh, Joseph A
- Graham, John M
- Lin, Angela E
- Katsanis, Nicholas
- Jones, Peter L
- Crowley, William F
- Davis, Erica E
- FitzPatrick, David R
- Talkowski, Michael E
Producer: 20170905
In:
Nature genetics vol. 49
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113.
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Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [electronic resource] by
- Shaw, Natalie D
- Brand, Harrison
- Kupchinsky, Zachary A
- Bengani, Hemant
- Plummer, Lacey
- Jones, Takako I
- Erdin, Serkan
- Williamson, Kathleen A
- Rainger, Joe
- Stortchevoi, Alexei
- Samocha, Kaitlin
- Currall, Benjamin B
- Dunican, Donncha S
- Collins, Ryan L
- Willer, Jason R
- Lek, Angela
- Lek, Monkol
- Nassan, Malik
- Pereira, Shahrin
- Kammin, Tammy
- Lucente, Diane
- Silva, Alexandra
- Seabra, Catarina M
- Chiang, Colby
- An, Yu
- Ansari, Morad
- Rainger, Jacqueline K
- Joss, Shelagh
- Smith, Jill Clayton
- Lippincott, Margaret F
- Singh, Sylvia S
- Patel, Nirav
- Jing, Jenny W
- Law, Jennifer R
- Ferraro, Nalton
- Verloes, Alain
- Rauch, Anita
- Steindl, Katharina
- Zweier, Markus
- Scheer, Ianina
- Sato, Daisuke
- Okamoto, Nobuhiko
- Jacobsen, Christina
- Tryggestad, Jeanie
- Chernausek, Steven
- Schimmenti, Lisa A
- Brasseur, Benjamin
- Cesaretti, Claudia
- García-Ortiz, Jose E
- Buitrago, Tatiana Pineda
- Silva, Orlando Perez
- Hoffman, Jodi D
- Mühlbauer, Wolfgang
- Ruprecht, Klaus W
- Loeys, Bart L
- Shino, Masato
- Kaindl, Angela M
- Cho, Chie-Hee
- Morton, Cynthia C
- Meehan, Richard R
- van Heyningen, Veronica
- Liao, Eric C
- Balasubramanian, Ravikumar
- Hall, Janet E
- Seminara, Stephanie B
- Macarthur, Daniel
- Moore, Steven A
- Yoshiura, Koh-Ichiro
- Gusella, James F
- Marsh, Joseph A
- Graham, John M
- Lin, Angela E
- Katsanis, Nicholas
- Jones, Peter L
- Crowley, William F
- Davis, Erica E
- FitzPatrick, David R
- Talkowski, Michael E
Publication details: Nature genetics 05 2017
In:
Nature genetics vol. 49
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114.
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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. [electronic resource] by
- Mak, Christopher C Y
- Doherty, Dan
- Lin, Angela E
- Vegas, Nancy
- Cho, Megan T
- Viot, Géraldine
- Dimartino, Clémantine
- Weisfeld-Adams, James D
- Lessel, Davor
- Joss, Shelagh
- Li, Chumei
- Gonzaga-Jauregui, Claudia
- Zarate, Yuri A
- Ehmke, Nadja
- Horn, Denise
- Troyer, Caitlin
- Kant, Sarina G
- Lee, Youngha
- Ishak, Gisele E
- Leung, Gordon
- Barone Pritchard, Amanda
- Yang, Sandra
- Bend, Eric G
- Filippini, Francesca
- Roadhouse, Chelsea
- Lebrun, Nicolas
- Mehaffey, Michele G
- Martin, Pierre-Marie
- Apple, Benjamin
- Millan, Francisca
- Puk, Oliver
- Hoffer, Mariette J V
- Henderson, Lindsay B
- McGowan, Ruth
- Wentzensen, Ingrid M
- Pei, Steven
- Zahir, Farah R
- Yu, Mullin
- Gibson, William T
- Seman, Ann
- Steeves, Marcie
- Murrell, Jill R
- Luettgen, Sabine
- Francisco, Elizabeth
- Strom, Tim M
- Amlie-Wolf, Louise
- Kaindl, Angela M
- Wilson, William G
- Halbach, Sara
- Basel-Salmon, Lina
- Lev-El, Noa
- Denecke, Jonas
- Vissers, Lisenka E L M
- Radtke, Kelly
- Chelly, Jamel
- Zackai, Elaine
- Friedman, Jan M
- Bamshad, Michael J
- Nickerson, Deborah A
- Reid, Russell R
- Devriendt, Koenraad
- Chae, Jong-Hee
- Stolerman, Elliot
- McDougall, Carey
- Powis, Zöe
- Bienvenu, Thierry
- Tan, Tiong Y
- Orenstein, Naama
- Dobyns, William B
- Shieh, Joseph T
- Choi, Murim
- Waggoner, Darrel
- Gripp, Karen W
- Parker, Michael J
- Stoler, Joan
- Lyonnet, Stanislas
- Cormier-Daire, Valérie
- Viskochil, David
- Hoffman, Trevor L
- Amiel, Jeanne
- Chung, Brian H Y
- Gordon, Christopher T
Producer: 20200818
In:
Brain : a journal of neurology vol. 143
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115.
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Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling. [electronic resource] by
- Johnson, Brett V
- Kumar, Raman
- Oishi, Sabrina
- Alexander, Suzy
- Kasherman, Maria
- Vega, Michelle Sanchez
- Ivancevic, Atma
- Gardner, Alison
- Domingo, Deepti
- Corbett, Mark
- Parnell, Euan
- Yoon, Sehyoun
- Oh, Tracey
- Lines, Matthew
- Lefroy, Henrietta
- Kini, Usha
- Van Allen, Margot
- Grønborg, Sabine
- Mercier, Sandra
- Küry, Sébastien
- Bézieau, Stéphane
- Pasquier, Laurent
- Raynaud, Martine
- Afenjar, Alexandra
- Billette de Villemeur, Thierry
- Keren, Boris
- Désir, Julie
- Van Maldergem, Lionel
- Marangoni, Martina
- Dikow, Nicola
- Koolen, David A
- VanHasselt, Peter M
- Weiss, Marjan
- Zwijnenburg, Petra
- Sa, Joaquim
- Reis, Claudia Falcao
- López-Otín, Carlos
- Santiago-Fernández, Olaya
- Fernández-Jaén, Alberto
- Rauch, Anita
- Steindl, Katharina
- Joset, Pascal
- Goldstein, Amy
- Madan-Khetarpal, Suneeta
- Infante, Elena
- Zackai, Elaine
- Mcdougall, Carey
- Narayanan, Vinodh
- Ramsey, Keri
- Mercimek-Andrews, Saadet
- Pena, Loren
- Shashi, Vandana
- Schoch, Kelly
- Sullivan, Jennifer A
- Pinto E Vairo, Filippo
- Pichurin, Pavel N
- Ewing, Sarah A
- Barnett, Sarah S
- Klee, Eric W
- Perry, M Scott
- Koenig, Mary Kay
- Keegan, Catherine E
- Schuette, Jane L
- Asher, Stephanie
- Perilla-Young, Yezmin
- Smith, Laurie D
- Rosenfeld, Jill A
- Bhoj, Elizabeth
- Kaplan, Paige
- Li, Dong
- Oegema, Renske
- van Binsbergen, Ellen
- van der Zwaag, Bert
- Smeland, Marie Falkenberg
- Cutcutache, Ioana
- Page, Matthew
- Armstrong, Martin
- Lin, Angela E
- Steeves, Marcie A
- Hollander, Nicolette den
- Hoffer, Mariëtte J V
- Reijnders, Margot R F
- Demirdas, Serwet
- Koboldt, Daniel C
- Bartholomew, Dennis
- Mosher, Theresa Mihalic
- Hickey, Scott E
- Shieh, Christine
- Sanchez-Lara, Pedro A
- Graham, John M
- Tezcan, Kamer
- Schaefer, G B
- Danylchuk, Noelle R
- Asamoah, Alexander
- Jackson, Kelly E
- Yachelevich, Naomi
- Au, Margaret
- Pérez-Jurado, Luis A
- Kleefstra, Tjitske
- Penzes, Peter
- Wood, Stephen A
- Burne, Thomas
- Pierson, Tyler Mark
- Piper, Michael
- Gécz, Jozef
- Jolly, Lachlan A
Producer: 20210106
In:
Biological psychiatry vol. 87
Availability: No items available.
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