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2013, The writings of Henry D. Thoreau, ISBN 9780691158921, v.
.... These letters provide an intimate view of Thoreau's path from college student to published author... 
Thoreau, Henry David, 1817-1862 | Intellectuals | Authors, American | Naturalists | Literary Collections | Letters
Book
by Marcogliese, Paul C and Shashi, Vandana and Spillmann, Rebecca C and Stong, Nicholas and Rosenfeld, Jill A and Koenig, Mary Kay and Martínez-Agosto, Julián A and Herzog, Matthew and Chen, Agnes H and Dickson, Patricia I and Lin, Henry J and Vera, Moin U and Salamon, Noriko and Graham, John M and Ortiz, Damara and Infante, Elena and Steyaert, Wouter and Dermaut, Bart and Poppe, Bruce and Chung, Hyung-Lok and Zuo, Zhongyuan and Lee, Pei-Tseng and Kanca, Oguz and Xia, Fan and Yang, Yaping and Smith, Edward C and Jasien, Joan and Kansagra, Sujay and Spiridigliozzi, Gail and El-Dairi, Mays and Lark, Robert and Riley, Kacie and Koeberl, Dwight D and Golden-Grant, Katie and Callens, Steven and Coucke, Paul and Dermaut, Bart and Hemelsoet, Dimitri and Poppe, Bruce and Steyaert, Wouter and Terryn, Wim and Van Coster, Rudy and Adams, David R and Alejandro, Mercedes E and Allard, Patrick and Azamian, Mahshid S and Bacino, Carlos A and Balasubramanyam, Ashok and Barseghyan, Hayk and Batzli, Gabriel F and Beggs, Alan H and Behnam, Babak and Bican, Anna and Bick, David P and Birch, Camille L and Bonner, Devon and Boone, Braden E and Bostwick, Bret L and Briere, Lauren C and Brown, Donna M and Brush, Matthew and Burke, Elizabeth A and Burrage, Lindsay C and Chen, Shan and Clark, Gary D and Coakley, Terra R and Cogan, Joy D and Cooper, Cynthia M and Cope, Heidi and Craigen, William J and D’Souza, Precilla and Davids, Mariska and Dayal, Jyoti G and Dell’Angelica, Esteban C and Dhar, Shweta U and Dillon, Ani and Dipple, Katrina M and Donnell-Fink, Laurel A and Dorrani, Naghmeh and Dorset, Daniel C and Douine, Emilie D and Draper, David D and Eckstein, David J and Emrick, Lisa T and Eng, Christine M and Eskin, Ascia and Esteves, Cecilia and Estwick, Tyra and Ferreira, Carlos and Fogel, Brent L and Friedman, Noah D and Gahl, William A and Glanton, Emily and Godfrey, Rena A and Goldstein, David B and Gould, Sarah E and Gourdine, Jean-Philippe F and Groden, Catherine A and Gropman, Andrea L and Haendel, Melissa and ... and Program for Undiagnosed Diseases (UD-PrOZA) and Undiagnosed Diseases Network and Undiagnosed Dis Network and Program Undiagnosed Dis UD-PrOZA
The American Journal of Human Genetics, ISSN 0002-9297, 08/2018, Volume 103, Issue 2, pp. 245 - 260
Interferon regulatory factor 2 binding protein-like (IRF2BPL) encodes a member of the IRF2BP family of transcriptional regulators. Currently the biological... 
CG11138 | ataxia | Drosophila | neurodegeneration | seizures | C3HC4 RING finger | developmental regression | pits | EAP1 | hypotonia | RECURRENT DE-NOVO | TRANSGENESIS | PROTEIN | UNDIAGNOSED DISEASES NETWORK | GENE | GENETICS & HEREDITY | ADRENOLEUKODYSTROPHY | MUTATIONS | EXPRESSION | DROSOPHILA | Physiological aspects | Nervous system | Development and progression | Genetic aspects | Degeneration | Research | Binding proteins
Journal Article
Frontiers in genetics, ISSN 1664-8021, 2018, Volume 9, p. 78
Journal Article
Frontiers in physiology, ISSN 1664-042X, 2016, Volume 7
...Author(s): Kenji Sanada, Jesus Montero-Marin, Marta Alda Diez, Montserrat Salas-Valero, Maria C. Perez-Yus, Hector Morillo, Marcelo M. P. Demarzo, Mauro Garcia... 
RCT | MBI | Healthy adult subjects | Salivary cortisol | Meta-analysis | Hydrocortisone | Health aspects | salivary cortisol | rct | healthy adult subjects
Journal Article
Ophthalmologica, ISSN 0030-3755, 12/2014, Volume 232, Issue 4, pp. 242 - 242
...Author Index Vol. 232, 2014 Ophthalmologica Abadia, B. 230 Abegão Pinto, L. 97 Aharrh-Gnama, A. 163 Arai, M. 118 Avitabile, T. 194 Ayrault, S. 216 Macor... 
Further Section
Journal Article
by Shashi, Vandana and Pena, Loren D.M and Kim, Katherine and Burton, Barbara and Hempel, Maja and Schoch, Kelly and Walkiewicz, Magdalena and McLaughlin, Heather M and Cho, Megan and Stong, Nicholas and Hickey, Scott E and Shuss, Christine M and Freemark, Michael S and Bellet, Jane S and Keels, Martha Ann and Bonner, Melanie J and El-Dairi, Maysantoine and Butler, Megan and Kranz, Peter G and Stumpel, Constance T.R.M and Klinkenberg, Sylvia and Oberndorff, Karin and Alawi, Malik and Santer, Rene and Petrovski, Slavé and Kuismin, Outi and Korpi-Heikkilä, Satu and Pietilainen, Olli and Aarno, Palotie and Kurki, Mitja I and Hoischen, Alexander and Need, Anna C and Goldstein, David B and Kortüm, Fanny and Bacino, A and Lee, Brendan H and Balasubramanyam, Ashok and Burrage, Lindsay C and Clark, Gary D and Craigen, William J and Dhar, Shweta U and Emrick, Lisa T and Graham, Brett H and Jain, Mahim and Lalani, Seema R and Lewis, Richard A and Moretti, Paolo M and Nicholas, Sarah K and Orange, Jordan S and Posey, Jennifer E and Potocki, Lorraine and Rosenfeld, Jill A and Scott, Daryl A and Hanchard, Neil A and Alyssa, Tran A and Mercedes, Alejandro E and Mashid, Azamian S and Bellen, Hugo J and Yamamoto, Shinya and Wangler, Michael F and Westerfield, Monte and Postlethwait, John H and Eng, Christine M and Yang, Yaping and Muzny, Donna M and Ward, Patricia A and Ramoni, Rachel B and McCray, Alexa T and Kohane, Issac S and Holm, Ingrid A and Might, Matthew and Mazur, Paul and Splinter, Kimberly and Esteves, Cecilia and Jiang, Yong-hui and McConkie-Rosell, Allyn and Spillmann, Rebecca C and Sullivan, Jennifer A and Walley, Nicole M and Beggs, Alan H and Loscalzo, Joseph and MacRae, Calum A and Silverman, Edwin K and Stoler, Joan M and Sweetser, David A and Maas, Richard L and Krier, Joel B and Rodan, Lance H and Walsh, Chris A and Cooper, Cynthia M and Pallais, Juan C and Donnell-Fink, Laurel A and Krieg, Elizabeth L and Lincoln, Sharyn A and Briere, Lauren C and Jacob, Howard J and Worthey, Elizabeth A and Lazar, Joe and Strong, Kim A and Handley, Lori H and ... and Undiagnosed Diseases Network and Undiagnosed Dis Network
American journal of human genetics, ISSN 0002-9297, 2016, Volume 99, Issue 4, pp. 991 - 999
The ASXL genes (ASXL1, ASXL2, and ASXL3) participate in body patterning during embryogenesis and encode proteins involved in epigenetic regulation and assembly... 
developmental delay | macrocephaly | glabellar nevus flammeus | whole-exome sequencing | intellectual disability | ASXL2 | INTELLECTUAL DISABILITY | BOHRING-OPITZ SYNDROME | GENOMICS | GENES | GENETICS & HEREDITY | HOMOLOG | MUTATIONS | RECIPROCAL REGULATION | FAMILY | Genetic variation | Health aspects | Phenotype
Journal Article
Npj genomic medicine, ISSN 2056-7944, 2019, Volume 4, Issue 1, pp. 1 - 1
...AUTHOR CORRECTION OPEN Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome Anne-Claude Tabet 1,2,3,4... 
Life Sciences | Genetics | Human genetics
Journal Article