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A case-controlled comparison of postoperative analgesic dosing between girls with Rett syndrome and girls with and without developmental disability undergoing spinal fusion surgery. [electronic resource] by
- Barney, Chantel C
- Merbler, Alyssa M
- Quest, Kelsey
- Byiers, Breanne J
- Wilcox, George L
- Schwantes, Scott
- Roiko, Samuel A
- Feyma, Timothy
- Beisang, Arthur
- Symons, Frank J
Producer: 20171004
In:
Paediatric anaesthesia vol. 27
Availability: No items available.
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Determining Electrode Placement for Transcranial Direct Current Stimulation: A Comparison of EEG- Versus TMS-Guided Methods. [electronic resource] by
- Rich, Tonya L
- Menk, Jeremiah S
- Rudser, Kyle D
- Chen, Mo
- Meekins, Gregg D
- Peña, Edgar
- Feyma, Timothy
- Bawroski, Kay
- Bush, Christina
- Gillick, Bernadette T
Producer: 20180724
In:
Clinical EEG and neuroscience vol. 48
Availability: No items available.
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The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2. [electronic resource] by
- Neul, Jeffrey L
- Benke, Timothy A
- Marsh, Eric D
- Skinner, Steven A
- Merritt, Jonathan
- Lieberman, David N
- Standridge, Shannon
- Feyma, Timothy
- Heydemann, Peter
- Peters, Sarika
- Ryther, Robin
- Jones, Mary
- Suter, Bernhard
- Kaufmann, Walter E
- Glaze, Daniel G
- Percy, Alan K
Producer: 20200309
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 180
Availability: No items available.
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19.
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Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. [electronic resource] by
- Peters, Sarika U
- Fu, Cary
- Suter, Bernhard
- Marsh, Eric
- Benke, Timothy A
- Skinner, Steve A
- Lieberman, David N
- Standridge, Shannon
- Jones, Mary
- Beisang, Arthur
- Feyma, Timothy
- Heydeman, Peter
- Ryther, Robin
- Kaufmann, Walter E
- Glaze, Daniel G
- Neul, Jeffrey L
- Percy, Alan K
Producer: 20200706
In:
Clinical genetics vol. 95
Availability: No items available.
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20.
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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
Availability: No items available.
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