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In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
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In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

Motahari, Zahra ; Moody, Sally Ann ; Maynard, Thomas Michael ; LaMantia, Anthony-Samuel

Journal of neurodevelopmental disorders, 2019-06, Vol.11 (1), p.7-28, Article 7 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
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Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome

Kippenhan, J. Shane ; Gregory, Michael D ; Nash, Tiffany ; Kohn, Philip ; Mervis, Carolyn B ; Eisenberg, Daniel P ; Garvey, Madeline H ; Roe, Katherine ; Morris, Colleen A ; Kolachana, Bhaskar ; Pani, Ariel M ; Sorcher, Leah ; Berman, Karen F

Journal of neurodevelopmental disorders, 2023-08, Vol.15 (1), p.1-29, Article 29 [Periódico revisado por pares]

London: BioMed Central Ltd

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3
Copy number variation at the 22q11.2 locus influences prevalence, severity, and psychiatric impact of sleep disturbance
Copy number variation at the 22q11.2 locus influences prevalence, severity, and psychiatric impact of sleep disturbance
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Copy number variation at the 22q11.2 locus influences prevalence, severity, and psychiatric impact of sleep disturbance

O'Hora, Kathleen P ; Lin, Amy ; Kushan-Wells, Leila ; Bearden, Carrie E

Journal of neurodevelopmental disorders, 2022-07, Vol.14 (1), p.41-16, Article 41 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders
Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders
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Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders

Rahn, Rachel M ; Weichselbaum, Claire T ; Gutmann, David H ; Dougherty, Joseph D ; Maloney, Susan E

Journal of neurodevelopmental disorders, 2021-03, Vol.13 (1), p.10-10, Article 10 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
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Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

Costain, Gregory ; Walker, Susan ; Argiropoulos, Bob ; Baribeau, Danielle A ; Bassett, Anne S ; Boot, Erik ; Devriendt, Koen ; Kellam, Barbara ; Marshall, Christian R ; Prasad, Aparna ; Serrano, Moises A ; Stavropoulos, D James ; Twede, Hope ; Vermeesch, Joris R ; Vorstman, Jacob A S ; Scherer, Stephen W

Journal of neurodevelopmental disorders, 2019-02, Vol.11 (1), p.3-3, Article 3 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Guanfacine treatment improves ADHD phenotypes of impulsivity and hyperactivity in a neurofibromatosis type 1 mouse model
Guanfacine treatment improves ADHD phenotypes of impulsivity and hyperactivity in a neurofibromatosis type 1 mouse model
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Guanfacine treatment improves ADHD phenotypes of impulsivity and hyperactivity in a neurofibromatosis type 1 mouse model

Lukkes, J L ; Drozd, H P ; Fitz, S D ; Molosh, A I ; Clapp, D W ; Shekhar, A

Journal of neurodevelopmental disorders, 2020-01, Vol.12 (1), p.2-13, Article 2 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Comparison of SHANK3 deficiency in animal models: phenotypes, treatment strategies, and translational implications
Comparison of SHANK3 deficiency in animal models: phenotypes, treatment strategies, and translational implications
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Comparison of SHANK3 deficiency in animal models: phenotypes, treatment strategies, and translational implications

Delling, Jan Philipp ; Boeckers, Tobias M

Journal of neurodevelopmental disorders, 2021-12, Vol.13 (1), p.55-55, Article 55 [Periódico revisado por pares]

England: BioMed Central Ltd

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