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Human Genetics:     more books (100)

Genetic Variation and Human Disease: Principles and Evolutionary Approaches (Cambridge Studies in Biological and Evolutionary Anthropology) by Kenneth M. Weiss, 1995-01-27 Human Genetics: Problems and Approaches by Friedrich Vogel, Arno G. Motulsky, 1996-08-14 Human Genetics for the Social Sciences (Advanced Psychology Text Series) by Dr. Gregory Carey, 2002-07-15 Genetics and the Search for Modern Human Origins by John H. Relethford, 2001-04-20 Human Oddities: A Book of Nature's Anomalies by Martin Monestier, 1987-10 Statistics in Human Genetics by Pak Sham, 1997-12-15 Is Human Nature Obsolete?: Genetics, Bioengineering, and the Future of the Human Condition (Basic Bioethics) Human Genetics (Genetics and Evolution) by Russ Hodge, 2010-01 Facilitating the Genetic Counseling Process: A Practice Manual (Volume 0) by Patricia McCarthy Veach, Bonnie S. LeRoy, et all 2003-08-14 Inside the Human Genome: A Case for Non-Intelligent Design by John C. Avise, 2010-02-12 Genes and Future People: Philosophical Issues in Human Genetics by Walter Glannon, 2002-01-01 Principles of Human Genetics (A Series of books in biology) by Curt Stern, 1973-06 On Genetic Interests: Family, Ethnicity, and Humanity in an Age of Mass Migration by Frank Kemp Salter, 2006-11-13 High-Yield Genetics (High-YieldSeries) by Ronald W. Dudek, John E. Wiley, 2008-06-18

lists with details

61. Department Of Human Genetics | University Of Chicago
    A department in the Biological Sciences Division.  
    http://www.genes.uchicago.edu/
    
    Extractions: Contact Us The Department of Human Genetics is the home within the Division of Biological Sciences for the study of basic principles of genetics and genomics as applied to human disease. We provide broad training in experimental genetics and genomics, statistical and population genetics, bioinformatics, and clinical genetics.  A common theme throughout our research is the application of basic genetic principles and strategies to the study of disease mechanism, disease susceptibility, and the genetic architecture of complex traits. Our faculty bridge between basic and clinical research and train students for careers in academia, industry, and medicine. T. Conrad Gilliam, Ph.D., Chairman Department of Human Genetics, University of Chicago

62. Human Genetics - Articles On Genetics | Buzzle.com
    Human Genetics Human genetics is the branch that studies the aspect of 'inheritance' in formation of human beings. Its study makes it easier to understand the cause of certain  
    http://www.buzzle.com/articles/human-genetics/

63. Case Western Reserve University - Department Of Epidemiology And Biostatistics
    Located in Cleveland, Ohio. Information on the department, graduate programs, courses, personnel, seminar series, and many links including one to The Human Genetic Analysis Resource site.  
    http://epbiwww.cwru.edu/

64. ASHG
    Informs health professionals, legislators, health policy makers, and the general public about all aspects of human genetics.  
    http://www.ashg.org/genetics/ashg/ashgmenu.htm

65. The Canadian Gene Cure Foundation : La Fondation Canadienne Gene Cure
    The CGCF supports excellence in core human genetics research and aims to raise funds to enable scientists to discover cures and treatments for genetic disorders. Find details about the programs and events, and contact information.  
    http://www.genecure.ca

66. Human Genetics - Virginia Commonwealth University Health System
    What to expect as a patient at MCV Hospitals; Maps and Directions; Request an Appointment; Pay Your Physician Bill Online; Financial Assistance / Counseling  
    http://www.vcuhealth.org/?id=68&sid=1

67. Scientists Identify The Gene For Familial Dysautonomia, A Degenerative Neurologi
    Scientists identify the gene for familial dysautonomia, a degenerative neurological disorder.  
    http://www.eurekalert.org/pub_releases/2001-01/TAJo-Sitg-1001101.php
    
    Extractions: The American Journal of Human Genetics In the March issue of The American Journal of Human Genetics, two groups report that mutations in the IKBKAP gene, encoding the protein IKAP, cause Familial Dysautonomia (FD). Two single base pair mutations in this gene account for nearly 100% of FD cases, and this finding will revolutionize genetic testing for this devastating disorder. FD is almost exclusively found in people of Ashkenazi Jewish origin, and it is estimated that 1 out of every 32 people in this population carry an FD mutation. People with two mutant copies of the IKBKAP gene show poor development of and degeneration of the sensory and autonomic nervous systems. The symptoms in these affected individuals include: abnormal sweating, hypertension, difficulty feeding and sucking, gastrointestinal dysfunction, and insensitivity to pain. FD is fatal; only 50% of patients reach age 30 years. The major FD mutation, which accounts for 99.5% of disease chromosomes, results in aberrant splicing of the IKBKAP RNA and thus the loss of one of the coding regions for the IKAP protein. A second, much less common mutation was found to cause a single amino acid change in a putative regulatory region of the protein. Together, these mutations are believed to account for all of the Ashkenazi Jewish cases of FD. With this finding, genetic testing for FD will become very effective and much less expensive.

68. VIRGINIA COMMONWEALTH UNIVERSITY : DEPARTMENT OF HUMAN & MOLECULAR GENETICS
    welcome to the virginia commonwealth university school of medicine department of human and molecular genetics  
    http://www.gen.vcu.edu/

69. Welcome To The Division Of Human Genetics - University Of Cape Town
    Contains departmental history, mission, staff and students.  
    http://web.uct.ac.za/depts/genetics/

70. Human Genetics Graduate Program Character
    Sarah Lawrence College established the first graduate program in human genetics in the United States. It remains the largest program of its kind in the country and has trained  
    http://www.slc.edu/graduate/programs/human-genetics/character/index.html

71. European Society Of Human Genetics: Home
    Promotes research in basic and applied human and medical genetics. Includes information on structure, courses, events, and membership.  
    http://www.eshg.org/
    
    Extractions: Home Sitemap Contact Join ESHG Search: Login: European Society of Human Genetics - ESHG is a non-profit organization. Its aims are to promote research in basic and applied human and medical genetics, to ensure high standards in clinical practice and to facilitate contacts between all persons who share these aims, particularly those working in Europe. The Society will encourage and seek to integrate research and its translation into clinical benefits and professional and public education in all areas of human genetics. Access the document Online abstract submission and registration are open Faculté de Médecine Paris-Sud, Kremlin Bicêtre, France

72. The Joan H. Marks Graduate Program In Human Genetics
    About. At a Glance; Overview. History of the College; Accreditation; The Campus; Campus Greening; College Leadership. Office of the President; Board of Trustees  
    http://www.slc.edu/graduate/programs/human-genetics/index.html

73. Human Genetics Information Center:
    Human Genetics Concepts and Applications, 7/e is a nonscience majors human genetics text that clearly explains what genes are, how they function, how they interact with the  
    http://highered.mcgraw-hill.com/sites/0072848537/information_center_view0/

74. Medical Research Council, Human Genetics Unit
    Undertakes research to obtain a molecular and cellular understanding of genetic factors implicated in human disease and normal and abnormal development.  
    http://www.hgu.mrc.ac.uk/
    
    Extractions: The Medical Research Council Human Genetics Unit is at the forefront of research into human genetics. Its role is to advance the understanding of genetic factors implicated in human disease and normal and abnormal development. The Unit's programmes of work cover the themes of developmental genetics, chromosome biology and models for human genetic diseases. The unit is one of the largest MRC research establishments supporting approximately 220 scientists, support staff, fellows, PhD students and visiting scientists. Class Prize for the MSc Biomedical Sciences programme

75. Homepage Source
    Independent body representing professionals working in research, and providing services to the public. Features news of activities, events and careers information.  
    http://www.bshg.org.uk/
    
    Extractions: Your browser does not support inline frames or is currently configured not to display inline frames. BSHG is an independent body representing UK human genetics professionals. Its constituent organisations are: Clinical Genetics Society (CGS) Association for Clinical Cytogenetics (ACC) Clinical Molecular Genetics Society (CMGS) Association of Genetic Nurses and Counsellors (AGNC) ... Society for Genomics, Policy and Population Health (SGPPH) What's new Society for Genomics Policy and Population Health On behalf of The Society for Genomics Policy and Population Health (SGPPH) please see attachment for further details on the forthcoming 5th AGM to be held on 30 November 2010, London. Please note that the deadline has been extended until 5 th November 2010 The British Society for Human Genetics is grateful for the opportunity to respond to the Public consultation on the revision of Directive 98/79/ec of the European Parliament and of the Council of 27 October 1998 on the IVD directive

76. The Biology Project: Human Biology
    Human Biology contains units on Blood Types, Color Blindness, Human Genetics, DNA Forensics, Human Reproduction, Birth Control, Sexually Transmitted Diseases, Web Karyotyping  
    http://www.biology.arizona.edu/human_Bio/human_bio.html
    
    Extractions: The Biology Project Home Human Biology Web Karyotyping ) Play the role of a cytogenetic technician and complete three patient karyotypes, then evaluate and diagnose each patient. For classroom use, teachers can download a printable Student Worksheet (requires Adobe Acrobat Reader New Methods in Karyotyping Learn about this exciting new technique for diagnosing chromosomal abnormalities. The Blackett Family DNA Activity Use this family study to learn the concepts and techniques behind DNA profiling , interpret DNA autoradiograms, and evaluate DNA profiles to determine familial relationships The Blackett Family DNA Activity 2 Use real Short Tandem Repeat (STR) DNA profiles to solve paternity and missing person cases in this inquiry-based activity.

77. The Cactus Project - Laura Cinti 2002
    The cactus project is a transgenic artwork involving the fusion of human genetic material into the cactus genome resulting in the cactus expressing human hair.  
    http://www.thecactusproject.com/

78. The Etruscans: A Population-Genetic Study
    A research paper published in the American Journal of Human Genetics, April 2004.  
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1181945/
    
    Extractions: window.name="mainwindow"; initRedirectClicks('/pmc/extredirect/') Journal List Am J Hum Genet v.74(4); Apr 2004 Am J Hum Genet. 2004 April; Published online 2004 March 10. PMCID: The Etruscans: A Population-Genetic Study Cristiano Vernesi, David Caramelli, Isabelle Dupanloup, Giorgio Bertorelle, Martina Lari, Enrico Cappellini, Jacopo Moggi-Cecchi, Brunetto Chiarelli, Antonella Casoli, Francesco Mallegni, Carles Lalueza-Fox, and Guido Barbujani Address for correspondence and reprints: Dr. Guido Barbujani, Dipartimento di Biologia, via Borsari 46, I-44100 Ferrara, Italy. E-mail: g.barbujani/at/unife.it Present affiliation: Centre integratif de genomique (CIG), Lausanne, Switzerland. Received December 5, 2003; Accepted January 28, 2004. This article has been cited by other articles in PMC. Abstract b.c. Introduction Analysis of genetic data in modern populations has proved to be a powerful tool for reconstructing crucial aspects of human evolutionary history (Cavalli-Sforza et al. ; Ingman et al.

79. Genentech
    Uses human genetic information to develop and manufacture pharmaceuticals such as growth hormones, tissue-plasminogen activators to dissolve blood clots, and cystic fibrosis therapeutics.  
    http://www.genentech.com/gene/index.jsp

80. Human Variation: Cause And Consequence
    Aims to explore human genetic and phenotypic variability in the light of recent developments in genomics, genetics and molecular medicine. 20 - 23 June, 2010 at Heidelberg, Germany.  
    http://www.embo-embl-symposia.org/symposia/2010/EES10-01/index.html
    
    Extractions: Download Poster The goal of this Symposium is to explore human genetic and phenotypic variability in the light of recent developments in genomics, genetics and molecular medicine. The topics covered will include the mechanisms of mutation, normal sequence variation from the DNA to the chromosomal level, functional polymorphism and disease genetics. Keynote Lectures will be delivered by Svante Pääbo, Max Planck Institute for Evolutionary Anthropology, and Kári Stefánsson, deCODE genetics. About 2010 Symposia Human Variation Speakers ... European Molecular Biology Laboratory

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