Results
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1.
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Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome. [electronic resource] by
- Fiksinski, Ania M
- Schneider, Maude
- Murphy, Clodagh M
- Armando, Marco
- Vicari, Stefano
- Canyelles, Jaume M
- Gothelf, Doron
- Eliez, Stephan
- Breetvelt, Elemi J
- Arango, Celso
- Vorstman, Jacob A S
Producer: 20191028
In:
American journal of medical genetics. Part A vol. 176
Availability: No items available.
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2.
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White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline. [electronic resource] by
- Nuninga, Jasper Olivier
- Bohlken, Marc Marijn
- Koops, Sanne
- Fiksinski, Ania M
- Mandl, René C W
- Breetvelt, Elemi J
- Duijff, Sasja N
- Kahn, René S
- Sommer, Iris E C
- Vorstman, Jacob A S
Producer: 20190412
In:
Psychological medicine vol. 48
Availability: No items available.
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3.
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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. [electronic resource] by
- Vervoort, Lisanne
- Demaerel, Wolfram
- Rengifo, Laura Y
- Odrzywolski, Adrian
- Vergaelen, Elfi
- Hestand, Matthew S
- Breckpot, Jeroen
- Devriendt, Koen
- Swillen, Ann
- McDonald-McGinn, Donna M
- Fiksinski, Ania M
- Zinkstok, Janneke R
- Morrow, Bernice E
- Heung, Tracy
- Vorstman, Jacob A S
- Bassett, Anne S
- Chow, Eva W C
- Shashi, Vandana
- Vermeesch, Joris R
Producer: 20200615
In:
Human molecular genetics vol. 28
Availability: No items available.
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4.
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Low prevalence of substance use in people with 22q11.2 deletion syndrome. [electronic resource] by
- Vingerhoets, Claudia
- van Oudenaren, Mathilde J F
- Bloemen, Oswald J N
- Boot, Erik
- van Duin, Esther D A
- Evers, Laurens J M
- Fiksinski, Ania M
- Breetvelt, Elemi J
- Palmer, Lisa D
- Vergaelen, Elfi
- Vogels, Annick
- Meijer, Carin
- Booij, Jan
- de Haan, Liewe
- Swillen, Ann
- Vorstman, Jacob A S
- Bassett, Anne S
- van Amelsvoort, Therese A M J
Producer: 20210604
In:
The British journal of psychiatry : the journal of mental science vol. 215
Availability: No items available.
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5.
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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2. [electronic resource] by
- Boot, Erik
- Butcher, Nancy J
- Udow, Sean
- Marras, Connie
- Mok, Kin Y
- Kaneko, Satoshi
- Barrett, Matthew J
- Prontera, Paolo
- Berman, Brian D
- Masellis, Mario
- Dufournet, Boris
- Nguyen, Karine
- Charles, Perrine
- Mutez, Eugénie
- Danaila, Teodor
- Jacquette, Aurélia
- Colin, Olivier
- Drapier, Sophie
- Borg, Michel
- Fiksinski, Ania M
- Vergaelen, Elfi
- Swillen, Ann
- Vogels, Annick
- Plate, Annika
- Perandones, Claudia
- Gasser, Thomas
- Clerinx, Kristien
- Bourdain, Frédéric
- Mills, Kelly
- Williams, Nigel M
- Wood, Nicholas W
- Booij, Jan
- Lang, Anthony E
- Bassett, Anne S
Producer: 20190812
In:
Neurology vol. 90
Availability: No items available.
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6.
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Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study. [electronic resource] by
- Villalón-Reina, Julio E
- Martínez, Kenia
- Qu, Xiaoping
- Ching, Christopher R K
- Nir, Talia M
- Kothapalli, Deydeep
- Corbin, Conor
- Sun, Daqiang
- Lin, Amy
- Forsyth, Jennifer K
- Kushan, Leila
- Vajdi, Ariana
- Jalbrzikowski, Maria
- Hansen, Laura
- Jonas, Rachel K
- van Amelsvoort, Therese
- Bakker, Geor
- Kates, Wendy R
- Antshel, Kevin M
- Fremont, Wanda
- Campbell, Linda E
- McCabe, Kathryn L
- Daly, Eileen
- Gudbrandsen, Maria
- Murphy, Clodagh M
- Murphy, Declan
- Craig, Michael
- Emanuel, Beverly
- McDonald-McGinn, Donna M
- Vorstman, Jacob A S
- Fiksinski, Ania M
- Koops, Sanne
- Ruparel, Kosha
- Roalf, David
- Gur, Raquel E
- Eric Schmitt, J
- Simon, Tony J
- Goodrich-Hunsaker, Naomi J
- Durdle, Courtney A
- Doherty, Joanne L
- Cunningham, Adam C
- van den Bree, Marianne
- Linden, David E J
- Owen, Michael
- Moss, Hayley
- Kelly, Sinead
- Donohoe, Gary
- Murphy, Kieran C
- Arango, Celso
- Jahanshad, Neda
- Thompson, Paul M
- Bearden, Carrie E
Producer: 20210315
In:
Molecular psychiatry vol. 25
Availability: No items available.
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