81. Tennessee Mouse Genome Consortium The Consortium s purpose is to promote mouse models for human genetic diseases and as subjects for the study of gene function. http://tnmouse.org

Home News Navigate Site About TMGC ... Neuromutagenesis Requests: Contact Dan Goldowitz for information about this project. Welcome to the TMGC Web Site "Pooling expertise and resources for the study of complex biological systems" The Tennessee Mouse Genome Consortium (TMGC) brings together expertise and resources across the state of Tennessee for the study of complex biological systems using mouse model systems. Our consortium includes a National Laboratory, several universities, and several medical research centers. Researchers from these institutions contribute their expertise in mouse genetics, basic biomedical research, clinical research, laboratory animal care, research administration, bioinformatics, and bioanalytical technologies. This mix brings a wide range of resources to bear on biomedical research and training. Webmaster Page last updated: Tuesday, April 06, 2010.

82. Rat Mapping Resources Links to genetic and radiation hybrid maps, markers and other resources from The Wellcome Trust Centre for Human Genetics. http://www.well.ox.ac.uk/rat_mapping_resources/

The Wellcome Trust Centre for Human Genetics Rat Mapping Resources Maps Markers Congenics Gene variants ... Links Maps SNP-based genetic maps of the Rat (Nature Genetics 40:560 - 566, 2008) Integration of Rat Linkage Maps in the Rat and Mouse Genomic Sequences (Genome Res. 14:758-65, 2004) Integrated Radiation Hybrid/Consensus Linkage/Gene map (Genomics 75:57-69, 2001) Rat Radiation Hybrid Maps (Nature Genetics 22: 27-36,1999) Oxford Rat Genetic Map 1997 (Genome Research 7: 434-440, May1997) Comparative Mapping 1-Radiation Hybrid Maps (Nature Genetics 22: 27-36, May1999) 2-Linkage Maps (Mammaliam Genome 10: 675-686,1999) 3-Detailed Gene Map of Rat Chromosome 1 (Genomics 64: 32-43, 2000) 4-Detailed Gene Map of locus on Rat Chromosome 8 (Human Molecular Genetics 11: 2165-73, 2002) Markers Marker Information SNPs SSLPs, others Polymorphism data SNPs SSLPs Congenics BN.GK- Nidd/gk1 (rat chromosome 1) (Mamm Genome 17:538-547, 2006) BN.GK- Nidd/gk2 (rat chromosome 2) (Physiol Genomics 19:1-10, 2004) BN.GK- Nidd/gk5 (rat chromosome 8) (Diabetologia 47:1096-1106, 2004) Sequence variations in disease candidate genes Functional SNPs in inbred rat strains Genomic organization of the rat Clock gene and sequence analysis in inbred rat strains (Genomics 87(2): 208-217, 2006)

83. WHO | The Genomic Resource Centre World Health Organization program which develops genetic approaches to the control of the most common hereditary diseases and those with a genetic predisposition. http://www.who.int/genomics/en/

Language options Search All WHO This site only Main navigation Home About WHO Countries Health topics ... Craniofacial anomalies Genomic resource centre About us Contact us Interns and volunteers Networks ... Programmes and projects Main content The Genomic Resource Centre The Genomic Resource Centre (GRC) has been developed by WHO's Human Genetics to provide information and to raise awareness on human genetics and more recently human genomics, a new and rapidly developing science. This site provides an overview of the issues and concerns around human genetics and public health and, in particular, addresses the ethical, legal and social implications (ELSI) of genomics. More about the GRC RESOURCES Ask the expert Full text Useful online resources for health professionals More information Educational tools for health professionals More information GENOMICS Genomics and policy More information International Database on Craniofacial Anomalies (IDCFA) More information Genetics and common diseases More information GENOMICS Resource submissions Submission form to include a resource in the GRC Add a resource Feedback forms Contact HGN Evaluate the GRC Publications Online and print documentation on human genomics and related areas Publications Media room Fact sheets, news and speeches

84. Eurogene Portal E-learning portal in the domain of human genetics. It provides learning resources including presentations, articles, images and video lectures, for statistical, medical and molecular genetics. http://eurogene.open.ac.uk

@import "/sites/all/modules/fivestar/css/fivestar.css"; @import "/modules/node/node.css"; @import "/modules/system/defaults.css"; @import "/modules/system/system.css"; @import "/modules/user/user.css"; @import "/sites/all/modules/event/event.css"; @import "/sites/all/modules/gallery/gallery.css"; @import "/sites/all/modules/gallery/gallery_filter.css"; @import "/sites/all/modules/graphstat/graphstat.css"; @import "/themes/pixelgreen/adt_pixelgreen/style.css"; @import "/sites/all/modules/search03/css/popup.css"; User login Username: Password: Create new account Request new password Navigation Latest resources Resources Search Topic browser Gallery Tools Topic viewer Ontology viewer About portal About Eurogene Take a quick tour Who and where Contact us Upcoming events American Society of Human Genetics (ASHG) 60th Annual Meeting (6 hours) ESGM: Course in Mitochondrial Metabolism and Cancer (1 day) MEDICA 2010 (15 days) 2nd International Conference of the Cyprus Society of Human Genetics (24 days) more RSS feed We'd like to inform you about new features of Eurogene portal: Newsletter - you can subscribe to get new resources directly to your email Exports - add resources to your social networks Citations - use Eurogene resources easily in your papers Search resources Advanced search Term: English French Spanish Lithuanian Italian Dutch Greek Czech German Topic: Any text field: Title: Author: Abstract: Text: Filters Resource types: Text Video Images Learning Package External resources Output languages: English French Spanish Lithuanian Italian

85. Human Genetics Program | Department Of Pediatrics | NYU Langone Medical Center Offers evaluation, testing and counseling for genetic diseases with information on faculty, clinical services, molecular genetics laboratory, and research interests http://www.med.nyu.edu/genetics/

@import "/genetics/sites/all/themes/purple_gradient_header/style.css"; NYU Langone Home Department of Pediatrics Site Map Genetics Home ... Directories Our high-profile research includes the Genetics of Sex Determination and the Jewish HapMap Project. Genetic counseling can identify a cause for an abnormality, and help determine your chances to conceive a normal baby. A genetics evaluation can identify and guide treatment of childhood and adult disorders, whether hereditary or not . Research Reproductive Counseling Medical Genetics Evaluation Human Genetics Program There is more to human sexual development than just X and Y chromosomes. NYU Human Genetics Program to offer investigational testing for disorders of sexual development. Learn more ... Learn more about the latest gene discovery Genetic Screening Sign-up for Students/Community Events Ensure that your children do not suffer from diseases including Tay-Sachs and Cystic Fibrosis by signing up for a genetic screening. Sign up now Pediatric Divisions Select a Division General Pediatrics Emergency Medicine Endrocrinology Epilepsy Center Familial Dysautonomia Hematology / Oncology Human Genetics Infectious Diseases Neonatology Surgical Subspecialties Quick Links A-Z Website Directory Careers Volunteer Opportunities The "LINK"

86. Moroccan Human Mutation Database The first catalog of human genetic disorders and mutations found in Moroccan population. This website has been created to provide clinicians and scientists access to a central genetic database for the local population. http://www.sante.gov.ma/Departements/INH/MoHuMuDa/index.htm

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87. UAB Heflin Center - Home Support genetic and genomic research at University of Alabama at Birmingham. Includes news, activities, facilities, and personnel. http://www.heflingenetics.uab.edu/

Organization Chart Home Center Facilities Genomic Core Sequencing Core SNP Genotyping DNA Profiling ... Bioinformatics Resources Partner Resources UAB Comprehensive Cancer Center Hudson Alpha Affymetrix Illumina ... Other Resources Membership Current Members Search Members Become A Member Contact Announcement UAB Questions About The Site?

88. Vanderbilt Program In Human Genetics Research aims to understand the part genes play in complex traits where there is an intricate interplay of multiple genes and environmental factors. Includes core facilities, news, education and careers. http://chgr.mc.vanderbilt.edu/

89. Laboratoire De Génétique Et Génomique Moléculaire Humaine - M.E. Samuels Dr Mark Samuels provides information on his research into the human genome, his publications and links. http://www.deptmed.umontreal.ca/samuels/

English Biographie Dr . Mark Samuels summa cum laude Princeton University , et son Ph.D. en biology de L'Institut de Technologie de Massachusetts , ou il travaillait avec Prof. Phillip Sharp. Drosophile Dr . Samuels est maintenant , et . Il est un

90. Anuranjan Anand - Home Focuses on exploring possible associations between genes and commonly occurring neurological and sensorineural disorders. Includes research, people, and publications. http://www.jncasr.ac.in/anand/

91. Center For Human Genetic Research- Massachusetts General Hospital Research at Massachusetts General Hospital includes the mapping and cloning of genes involved in many genetic disorders. http://www2.massgeneral.org/chgr/

The Center for Human Genetic Research (CHGR) is a multidisciplinary cross-departmental center whose central mission is promotion of the genetic research cycle:

92. Human Genetics Society Of Australasia Promote standards, research, and education. Includes constitution and policies, special interest groups, listing of certified DNA laboratories, and links to other societies. http://www.hgsa.com.au/

var icl_lang = 'en';var icl_home = 'http://www.hgsa.org.au'; Home Home Contact Us Site Map ... Log in Human Genetics Society of Australasia About Become a member HGSA Structure HGSA Committees ... Training Certification Biochemical Genetics Clinical Genetics Cytogenetics Genetic Counselling ... Links The Human Genetics Society of Australasia was formed in 1977 to provide a forum for the various disciplines collected under the title of Human Genetics, clinical genetics, cytogenetics, genetic counselling, molecular genetics, biochemical genetics, newborn screening, neurogenetics and cancer genetics. Recent News HGSA Council 9 December 2009 by Secretariat The Council consists of the Executive plus annually elected representatives of each branch and special interest group. President: A/Prof Julie McGaughran Continue Reading... Category: Committees Featured HGSA Fellowship Qualification 17 September 2010 by Secretariat Should you be one of the members affected by this please use the attached pdf file as verification. Fellowship verification letter Continue Reading...

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