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Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2). [electronic resource] by
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Producer: 20151022
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Clinical genetics vol. 87
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Genomic Differentiation during Speciation-with-Gene-Flow: Comparing Geographic and Host-Related Variation in Divergent Life History Adaptation in [electronic resource] by
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Publication details: Genes May 2018
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Optogenetic Tractography for anatomo-functional characterization of cortico-subcortical neural circuits in non-human primates. [electronic resource] by
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Producer: 20190916
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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. [electronic resource] by
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Producer: 20090528
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Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. [electronic resource] by
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Comparing fully automated state-of-the-art cerebellum parcellation from magnetic resonance images. [electronic resource] by
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- Ben Ayed, Ismail
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- Thyreau, Benjamin
- Romero, José E
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- Collins, D Louis
- Ying, Sarah H
- Onyike, Chiadi U
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A branched-chain amino acid metabolite drives vascular fatty acid transport and causes insulin resistance. [electronic resource] by
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- Kim, Boa
- Ibrahim, Ayon
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- Jiang, Aihua
- Chu, Qingwei
- Forman, Daniel E
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- Krishnaiah, Saikumari
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Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications. [electronic resource] by
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- Kleefstra, T
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- Sheffield, L J
- Zuffardi, O
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Publication details: Molecular syndromology 2010
In:
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Enhancing studies of the connectome in autism using the autism brain imaging data exchange II. [electronic resource] by
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- Beggiato, Anita
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- Bookheimer, Susan Y
- Braden, B Blair
- Byrge, Lisa
- Castellanos, F Xavier
- Dapretto, Mirella
- Delorme, Richard
- Fair, Damien A
- Fishman, Inna
- Fitzgerald, Jacqueline
- Gallagher, Louise
- Keehn, R Joanne Jao
- Kennedy, Daniel P
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- Luna, Beatriz
- Mostofsky, Stewart H
- Müller, Ralph-Axel
- Nebel, Mary Beth
- Nigg, Joel T
- O'Hearn, Kirsten
- Solomon, Marjorie
- Toro, Roberto
- Vaidya, Chandan J
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Producer: 20180223
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Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. [electronic resource] by
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- Wilkie, A O M
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In:
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Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. [electronic resource] by
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Producer: 20091102
In:
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Toward discovery science of human brain function. [electronic resource] by
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- Mennes, Maarten
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- Ernst, Monique
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- Hoptman, Matthew J
- Hyde, James S
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- Kötter, Rolf
- Li, Shi-Jiang
- Lin, Ching-Po
- Lowe, Mark J
- Mackay, Clare
- Madden, David J
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- Margulies, Daniel S
- Mayberg, Helen S
- McMahon, Katie
- Monk, Christopher S
- Mostofsky, Stewart H
- Nagel, Bonnie J
- Pekar, James J
- Peltier, Scott J
- Petersen, Steven E
- Riedl, Valentin
- Rombouts, Serge A R B
- Rypma, Bart
- Schlaggar, Bradley L
- Schmidt, Sein
- Seidler, Rachael D
- Siegle, Greg J
- Sorg, Christian
- Teng, Gao-Jun
- Veijola, Juha
- Villringer, Arno
- Walter, Martin
- Wang, Lihong
- Weng, Xu-Chu
- Whitfield-Gabrieli, Susan
- Williamson, Peter
- Windischberger, Christian
- Zang, Yu-Feng
- Zhang, Hong-Ying
- Castellanos, F Xavier
- Milham, Michael P
Producer: 20100512
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 107
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