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by Prado-Martinez, Javier and Sudmant, Peter H and Kidd, Jeffrey M and Li, Heng and Kelley, Joanna L and Lorente-Galdos, Belen and Veeramah, Krishna R and Woerner, August E and O’Connor, Timothy D and Santpere, Gabriel and Cagan, Alexander and Theunert, Christoph and Casals, Ferran and Laayouni, Hafid and Munch, Kasper and Hobolth, Asger and Halager, Anders E and Malig, Maika and Hernandez-Rodriguez, Jessica and Hernando-Herraez, Irene and Prüfer, Kay and Pybus, Marc and Johnstone, Laurel and Lachmann, Michael and Alkan, Can and Twigg, Dorina and Petit, Natalia and Baker, Carl and Hormozdiari, Fereydoun and Fernandez-Callejo, Marcos and Dabad, Marc and Wilson, Michael L and Stevison, Laurie and Camprubí, Cristina and Carvalho, Tiago and Ruiz-Herrera, Aurora and Vives, Laura and Mele, Marta and Abello, Teresa and Kondova, Ivanela and Bontrop, Ronald E and Pusey, Anne and Lankester, Felix and Kiyang, John A and Bergl, Richard A and Lonsdorf, Elizabeth and Myers, Simon and Ventura, Mario and Gagneux, Pascal and Comas, David and Siegismund, Hans and Blanc, Julie and Agueda-Calpena, Lidia and Gut, Marta and Fulton, Lucinda and Tishkoff, Sarah A and Mullikin, James C and Wilson, Richard K and Gut, Ivo G and Gonder, Mary Katherine and Ryder, Oliver A and Hahn, Beatrice H and Navarro, Arcadi and Akey, Joshua M and Bertranpetit, Jaume and Reich, David and Mailund, Thomas and Schierup, Mikkel H and Hvilsom, Christina and Andrés, Aida M and Wall, Jeffrey D and Bustamante, Carlos D and Hammer, Michael F and Eichler, Evan E and Marques-Bonet, Tomas
Nature (London), ISSN 1476-4687, 2013, Volume 499, Issue 7459, pp. 471 - 475
Journal Article
PLoS genetics, ISSN 1553-7404, 2012, Volume 8, Issue 1, p. e1002473
Journal Article
Human gene therapy, ISSN 1557-7422, 2008, Volume 19, Issue 10, pp. 979 - 990
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 3/2012, Volume 109, Issue 13, pp. 4980 - 4985
.... Here we report homozygosity mapping of an infantile neurodegenerative disease locus in a genetic isolate... 
Retrotransposons | Nervous system diseases | MicroRNA | Transposons | RNA | Small interfering RNA | Genetic loci | Encephalopathies | Genetic mutation | Sequencing | Pediatrics | Medulla oblongata | Long noncoding RNA | Long interspersed element 1 | Genetic disease | long interspersed element 1 | MULTIDISCIPLINARY SCIENCES | IDENTIFICATION | PREDICTION | ELEMENTS | pediatrics | GENES | SEQUENCE | DISEASE | long noncoding RNA | SIGNAL RECOGNITION PARTICLE | CENTRAL-NERVOUS-SYSTEM | genetic disease | EXPRESSION | medulla oblongata | BRAIN | Geography | Chromosomes, Human, Pair 8 - genetics | Conserved Sequence - genetics | Genes, Recessive - genetics | Humans | Brain Diseases - genetics | Molecular Sequence Data | Nucleotides - genetics | Infant | Anorexia - genetics | Genetic Loci | Anorexia - complications | RNA, Untranslated - genetics | Retroelements - genetics | Young Adult | Base Sequence | RNA, Untranslated - chemistry | Nucleic Acid Conformation | Introns - genetics | Indian Ocean | Chromosome Mapping | Mutation - genetics | Disease Progression | Magnetic Resonance Imaging | Phenotype | Primates - genetics | Animals | Brain Diseases - pathology | Brain Diseases - complications | Chromosome Segregation - genetics | Encephalopathy | Physiological aspects | Development and progression | Genetic aspects | Health aspects | Life Sciences | Human health and pathology | Neurons and Cognition | Neurobiology | Genetics | Human genetics | Biological Sciences
Journal Article
Nature (London), ISSN 1476-4687, 2012, Volume 483, Issue 7387, pp. 82 - 86
Journal Article
2003, Studies in the evolution of language, ISBN 0199244839, Volume 3., 416
What is it that makes us human?; This is one of the most challenging and important questions we face. Our species' defining characteristic is language - we... 
Origin | Language and languages | Anthropological linguistics | Historical linguistics | Linguistic change
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