61![Research Paper The risk for major depression conferred by childhood maltreatment is multiplied by BDNF and SERT genetic vulnerability: a replication study Blanca Gutiérrez, PhD; Juan Ángel Bellón, MD, PhD; Margarita Research Paper The risk for major depression conferred by childhood maltreatment is multiplied by BDNF and SERT genetic vulnerability: a replication study Blanca Gutiérrez, PhD; Juan Ángel Bellón, MD, PhD; Margarita](https://www.pdfsearch.io/img/ab26640b976258c91b9cd7333556b7ca.jpg) | Add to Reading ListSource URL: jpn.caLanguage: English - Date: 2014-12-15 12:52:37
|
---|
62![Hidden burden: Most people carry recessive disease mutations Hidden burden: Most people carry recessive disease mutations](https://www.pdfsearch.io/img/e08face452bd3a7f274af1f7c61fcf40.jpg) | Add to Reading ListSource URL: medicalxpress.comLanguage: English - Date: 2015-05-03 22:57:04
|
---|
63![Chapter from: Genetic and Cultural Evolution of Cooperation Edited by P. Hammerstein, 2003 ISBN © The MIT Press 6 Chapter from: Genetic and Cultural Evolution of Cooperation Edited by P. Hammerstein, 2003 ISBN © The MIT Press 6](https://www.pdfsearch.io/img/7e21b3e339a7996fd78f2f0b7a29be82.jpg) | Add to Reading ListSource URL: anthro.vancouver.wsu.eduLanguage: English - Date: 2008-10-09 13:18:21
|
---|
64![Candidate Endophenotypes for Genetic Studies of Suicidal Behavior Candidate Endophenotypes for Genetic Studies of Suicidal Behavior](https://www.pdfsearch.io/img/e8ad845ae13383e57b86463aa1304de7.jpg) | Add to Reading ListSource URL: champagnelab.psych.columbia.eduLanguage: English - Date: 2009-04-14 10:45:18
|
---|
65![Many neuropsychiatric disorders have a strong genetic component. Genome wide association studies lead by international consortia has been building a list of genes common to multiple psychiatric disorders as well as those Many neuropsychiatric disorders have a strong genetic component. Genome wide association studies lead by international consortia has been building a list of genes common to multiple psychiatric disorders as well as those](https://www.pdfsearch.io/img/37ff702c11ddb2cea27d9dc03cfc4fff.jpg) | Add to Reading ListSource URL: wpi-iiis.tsukuba.ac.jp- Date: 2015-01-16 00:50:03
|
---|
66![REVIEWS Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity Lynn K. Paul*‡, Warren S. Brown‡, Ralph Adolphs*, J. Michael Tyszka*, REVIEWS Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity Lynn K. Paul*‡, Warren S. Brown‡, Ralph Adolphs*, J. Michael Tyszka*,](https://www.pdfsearch.io/img/35bf27ac7ac63863b9524e927da444b0.jpg) | Add to Reading ListSource URL: www.emotion.caltech.eduLanguage: English - Date: 2007-05-03 19:59:22
|
---|
67![Journal of IMAB - Annual Proceeding (Scientific Papers) 2008, book 2 CLINICAL AND GENETIC PECULIARITIES OF ISOLATED CLEFT PALATES Vera Krumova Department of Orthodontics, Faculty of dental Medicine, Journal of IMAB - Annual Proceeding (Scientific Papers) 2008, book 2 CLINICAL AND GENETIC PECULIARITIES OF ISOLATED CLEFT PALATES Vera Krumova Department of Orthodontics, Faculty of dental Medicine,](https://www.pdfsearch.io/img/81fff0de6aebf2c91b93a6a4833d78ff.jpg) | Add to Reading ListSource URL: www.journal-imab-bg.orgLanguage: English - Date: 2013-03-28 12:37:12
|
---|
68![Department of Health and Human Services - Muscula Dystrophies Department of Health and Human Services - Muscula Dystrophies](https://www.pdfsearch.io/img/5e43a8bc017cd8d38bfc2291abd2725e.jpg) | Add to Reading ListSource URL: mdcc.nih.govLanguage: English - Date: 2015-02-02 09:29:53
|
---|
69![SignatureChipOS® / PrenatalChip®OS Disorders Tested Clinically recognized regions of the genome assayed by the SignatureChipOS®(v3) / Signature PrenatalChip®OS(v3) The SignatureChipOS® / PrenatalChip®OS is a “wh SignatureChipOS® / PrenatalChip®OS Disorders Tested Clinically recognized regions of the genome assayed by the SignatureChipOS®(v3) / Signature PrenatalChip®OS(v3) The SignatureChipOS® / PrenatalChip®OS is a “wh](https://www.pdfsearch.io/img/df80450cd0e411303f743c58f59db0d9.jpg) | Add to Reading ListSource URL: www.obsgyn.hku.hkLanguage: English - Date: 2013-09-13 00:32:30
|
---|
70![What causes these conditions? Cystic fibrosis, PKU and other amino acid metabolism disorders, galactosaemia and FAODs are genetic disorders. These conditions are inherited from two healthy carrier parents, each carrying What causes these conditions? Cystic fibrosis, PKU and other amino acid metabolism disorders, galactosaemia and FAODs are genetic disorders. These conditions are inherited from two healthy carrier parents, each carrying](https://www.pdfsearch.io/img/1064c7885289126829677b95b12a9771.jpg) | Add to Reading ListSource URL: www.wch.sa.gov.auLanguage: English - Date: 2010-12-14 22:11:44
|
---|