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         Genetic Publications:     more books (100)
  1. Genetics, Biotechnology and Breeding of Maize and Sorghum (Special Publication / Royal Society of Chemistry)
  2. Darwin and the humanities, (Psychological review publications. Library of genetic science and philosophy) by James Mark Baldwin, 1909
  3. Newborn screening for genetic-metabolic diseases: Progress, principles and recommendations (DHEW publication ; no) by Neil A Holtzman, 1977
  4. Genetic Engineering-Biotechnology Sourcebook by Newsletter Publications Center, 1982-05
  5. Social and psychological aspects of applied human genetics: A bibliography, (DHEW publication no) by James R Sorenson, 1972
  6. Genetic engineering: Fast forwarding to future foods (Publication) by John Henkel, 1996
  7. A bibliography on forest genetics and forest trees improvement, 1956-1957 (Miscellaneous publication / United States Department of Agriculture) by Jonathan W Wright, 1960
  8. Introduction to Medical Genetics (Oxford Medical Publications) by J. A. Fraser; Pembrey, Marcus E. Roberts, 1985
  9. An introduction to medical genetics (Oxford medical publications) by John Alexander Fraser Roberts, 1973
  10. Stroke Genetics (Oxford Medical Publications) by Hugh Markus, 2003
  11. Introduction to Medical Genetics (Oxford Medicine Publications) by John Alexander Fraser Roberts, 1970
  12. An introduction to genetic statistics (Wiley publications in statistics) by Oscar Kempthorne, 1957
  13. Needs and strategies for genetic control: Municipal wastes (Publication) by Bruce E Rittmann, 1984
  14. Human genetics for medical students by M. M Dadone, 1980

81. Laboratory Of Molecular Biology, Genetic Analysis & Modelling - Publications & C
Laboratory of Molecular Biology, genetic Analysis Modelling publications Communications.
http://www.crp-sante.lu/en/LBMAGM_Publications.shtml
Introduction Organization Scientific Activities Collaborations ... Publications
Publications 2000-2003 Most of the data reported in the publications mentioned below have been obtained by Dr. Evelyne Friederich and colleagues at the Curie Institute, Paris as well as by associated collaborators. The work has been completed in Luxembourg.
  • Expression patterns of L-plastin isoform in normal and carcinomatous breast tissues. Lapillonne, A., Coué, O., Friederich, E., Nicolas, A., Del Maestro, L., Louvard, D., Robine, S., and X. Sastre-Garau. Anticancer Research (2000) Anticancer Research. 20: 3177-3182. Identification of an ActA and human zyxin actin polymerisation activity that is independent of the Arp2/3 complex. Fradelizi, J., Noireaux, V., Menichi, B., Louvard, D., Prost, J., Sykes C., Golsteyn, RM., and E. Friederich. (2001) Nature Cell Biol. 3:699-707. Targeting of zyxin to sites of actin membrane interaction and to the nucleus. Nix, D.A., Fradelizi, J., Bockholt, S., Louvard, D., Friederich, E., and M.C. Beckerle (2001) J. Biol. Chem. 276:34759-67. Villin. Robine, S., Louvard, D:, and Evelyne Friederich (2002). In Wiley Encyclopedia of Molecular Medecine, 5:3364-3365.

82. IPGRI Publication : Seeds And Survival: Crop Genetic Resources In War And Recon
Considers the impact of war, civil strife and lowintensity conflict on the management of plant genetic resources, in regions where crop plant genetic resources are still conserved in situ by small-scale agriculturalists. PDF format.
http://www.ipgri.cgiar.org/publications/pubfile.asp?ID_PUB=245

83. Guidelines For Genetic Registers And Associated Genetic Material (1999)
up, and the collection and storage of genetic material in association with a geneticregister. How to order http//www.nhmrc.gov.au/publications/order.htm.
http://www.health.gov.au/nhmrc/publications/synopses/e14syn.htm
For text only browsers, click here to see full site index
Guidelines for Genetic Registers and Associated Genetic Material (1999)
Synopsis of an NHMRC publication - Full copy available here in PDF (239KB) The purpose of the Guidelines is to provide guidance to those intending to establish a genetic register, Human Research Ethics Committees that are asked to approve the establishment of a genetic register, and institutions and organisations in which a genetic register is to be established. The document identifies matters for ethical consideration that relate to the establishment and operation of a genetic register. These include administrative arrangements, recruitment of registrants, consent, confidentiality and privacy, how family members may be approached, security, amalgamation and winding up, and the collection and storage of genetic material in association with a genetic register. How to order: http://www.nhmrc.gov.au/publications/order.htm

84. Developments Towards Participatory Forest Management On Mount Cameroon
The Limbe Botanic Garden and Rainforest genetic Conservation Project, 19881994. In PDF format only.
http://www.odifpeg.org.uk/publications/rdfn/17/rdfn-17d.pdf

85. Ethical Aspects Of Human Genetic Testing – An Information Paper
glossary and a list of Australian sources of information about genetic testing arealso included. How to order http//www.nhmrc.gov.au/publications/order.htm.
http://www.health.gov.au/nhmrc/publications/synopses/e39syn.htm
For text only browsers, click here to see full site index
Ethical Aspects of Human Genetic Testing – an Information Paper
Synopsis of an NHMRC publication - Full copy available here in PDF (453kb) Ethical Aspects of Human Genetic Testing – an Information Paper focuses on the key ethical issues related to genetic testing, such as obtaining consent, counselling, and privacy and confidentiality matters. Some basic information about the technical aspects of genetic testing is also provided as background to the ethical issues. A bibliography, glossary and a list of Australian sources of information about genetic testing are also included. How to order: http://www.nhmrc.gov.au/publications/order.htm - These documents are provided as Adobe Acrobat PDF files or Microsoft PowerPoint files. If you wish to view the PDF files you will need to install the Adobe Acrobat Reader on your computer to view them. The Adobe Acrobat Reader is available free of charge from Adobe's website ^ to top URL : http://www.nhmrc.gov.au/

86. Cat Genome Project - Laboratory Of Genomic Diversity
Features genetic markers and maps, animal model, and publications. maintained by the Laboratory of Genomic Diversity at the National Cancer Insitute.
http://home.ncifcrf.gov/ccr/lgd/comparative_genome/catgenome/index_n.asp
ABOUT LGD STAFF PUBLICATIONS PROJECTS ...
by Topic
Research Human Genetics MALD Project Comparative Genomic Cat Maps FIV Wildlife Bioinformatics Courses 2004:
Conservation Genetics

Aug. 16-27, 2004
Conferences 2003:
AGA Conservation
Genetics Conference

Cat Genome Project

Why The Cat
...
Links

Welcome to the Cat Genome Project, located at the National Cancer Institute / Frederick Cancer Research and Development Center, Frederick, MD. The project is maintained by the Laboratory of Genomic Diversity. Our research focuses on development of the cat as an animal model for human hereditary disease, infectious disease, genome evolution, comparative research initiatives within the family Felidae , and forensic potential. CCR Home About CCR Clinical Trials Research ... Accessibility

87. Genetics And Neuromuscular Diseases
HOW ARE genetic DISORDERS INHERITED? Then, the two recessive genes can come togetherin a child and produce the signs and symptoms of a genetic disorder.
http://www.mdausa.org/publications/gen_inhr.html
New 4/00 GENETICS
Genetics and Neuromuscular Diseases
Introduction
What is a Genetic Disorder? What is Genetic Testing? How are Genetic Disorders Inherited? ... MDA's Purpose and Programs HOW ARE GENETIC DISORDERS INHERITED?
Long before the advent of genetic testing or even complete understanding of DNA and RNA, astute observers noticed that genetic traits, including many disorders, were passed from one generation to another in somewhat predictable patterns. These came to be known as autosomal dominant, autosomal recessive, X-linked recessive and X-linked dominant patterns of inheritance. To understand heredity, you have to know a little about human chromosomes and how they work. Chromosomes come in pairs in the cell's nucleus. Humans have 46 chromosomes in each cell nucleus, which are actually 23 pairs of chromosomes. For 22 of these pairs, numbered chromosome 1 through chromosome 22, the chromosomes are the same; that is, they carry genes for the same traits. One chromosome comes from a person's mother, the other from his father. The 23rd pair is an exception and determines gender. The 23rd chromosomal pair differs according to whether you're a male or a female. Males have an X and a Y chromosome, while females have two Xs for this 23rd pair of chromosomes. Every female gets one X chromosome from her mother and one X from her father. Every male gets an X chromosome from his mother and a Y from his father. Y chromosomes are unique to males and, in fact, determine maleness. If a man passes to his child an X chromosome from this 23rd pair, it will be a girl; if he donates a Y, it will be a boy.

88. Center For Complex Systems Research
Founded in 1986, the Center for Complex Systems Research studies systems that display adaptive, selforganizing behavior and systems that are usually characterized by a large throughput, such as turbulent flow, lightning, and the flow of information through the internet. Models and techniques drawn from nonlinear dynamics and chaos, neural nets, cellular automata, artificial life, and genetic algorithms are then developed to describe these complex systems. A collection of technical reports and scientific publications of CCSR researchers is available.
http://www.ccsr.uiuc.edu
Center for Complex Systems Research
University of Illinois
ABOUT PEOPLE RESEARCH EDUCATION SEMINAR/SYMPOSIUM ... RECENT PUBLICATIONS
The Center for Complex Systems Research (CCSR) studies systems that display adaptive, self-organizing behavior and systems that are usually characterized by a large throughput, such as turbulent flow, lightning, and the flow of information through the internet. We develop models and techniques drawn from nonlinear dynamics and chaos, neural nets, cellular automata, artificial life, and genetic algorithms to describe these complex systems. Each year CCSR organizes and hosts the conference Understanding Complex Systems The Center for Complex Systems Research has a rich history. Founded in 1986 by Stephen Wolfram, the center was later led by Norman Packard and E. Atlee Jackson. A collection of technical reports and scientific publications of CCSR researchers ranging from cellular automata to entrainment control of chaos, experimental studies of turbulent flows, chaotic electronic circuits, and fractal agglomeration patterns is available. The research at CCSR is supported by the National Science Foundation Grant No. NSF PHY 01-40179, NSF DMS 03-25939 ITR, and NSF DGE 03-38215

89. MDA / Quest Vol 7 No 2 / Genetic Counselors Do It All
QUEST Volume 7, Number 2, April 2000. INFORMATION AND SUPPORT genetic CounselorsDo It All. by Margaret Wahl. There was no way to do genetic testing.
http://www.mdausa.org/publications/Quest/q72genetic.htm
Current Issue Back Issues Stories by Topic Research Stories ... Contents of This Issue
QUEST
Volume 7, Number 2, April 2000 INFORMATION AND SUPPORT
Genetic Counselors Do It All by Margaret Wahl
Genetic counselor Katie Leonard (right) helps a couple understand how genes are inherited. Pam Rhatigan remembers the day in 1981 when she and her husband, Brian, finished their genetic counseling sessions at the University of Arizona's medical center. They'd gone to discuss the chances that a baby they might conceive could be born with spinal muscular atrophy, a genetic disorder of muscle-controlling nerve cells that Pam was born with in 1953. There was no family history and little information of any kind, other than that the disorder was most likely recessive (requiring two genes, usually one from each parent). "They didn't even know what chromosome it was on," Rhatigan recalls. "There was no way to do genetic testing. There were so many unknowns that it was difficult to make an informed decision." The Rhatigans went straight from their last counseling session to Pizza City, a Tucson restaurant, where they flipped a coin to decide whether Pam would bear their child. "Luckily for our son, the quarter came up heads, "Rhatigan says. Paul, born the following year, appears to have escaped SMA.

90. NIH Rat Genomics And Genetics
Serves as a central point for information on NIH sponsored and related rat genetic and genomic activities and resources. Includes courses and meetings, reports and publications, and related resources.
http://www.nih.gov/science/models/rat/
Welcome to the NIH Rat Genomics and Genetics Web site. Suggestions for improving the Web page and for items to include are most welcome. We want this page to serve your interests. Comments may be relayed to Bettie Graham at bettie_graham@nih.gov Chairperson, Rat Genome Working Group: Stephen C. Mockrin, PH. D
Director, Divison of Heart and Vascular Diseases
National Heart, Lung, and Blood Institute
Photo Credit:
Dr. Marga Kujpers
Nature Genetics

91. Genetic Screening In The Workplace
Issues in Ethics V. 4, N. 2 Fall 1991. Read My Genes genetic Screening inthe Workplace. But none is likely to spark more debate than genetic tests.
http://www.scu.edu/ethics/publications/iie/v4n2/genes.html
About the Center Events Ethics Home
Focus Areas
...
Site Index
Issues in Ethics - V. 4, N. 2 Fall 1991
Read My Genes:
Genetic Screening in the Workplace
By Claire Andre and Manuel Velasquez
Few employment practices have stirred as much controversy as employment testing. From psychological questionnaires to urine samples, the devices used by employers to screen, select, and place workers have been challenged by civil rights groups and courts alike. But none is likely to spark more debate than genetic tests. These tests can detect the presence of genetic abnormalities in healthy individuals that may place those individuals at increased risk for developing certain diseases. In the workplace, such tests can be used to screen job applicants and employees who, because of their genetic makeup, may be more likely to develop diseases if exposed to certain worksite substances, such as chemicals or radiation. Research to date has identified about fifty genetic disorders thought to increase a person's susceptibility to the toxic or carcinogenic effects of environmental agents. Individuals with the sickle cell trait, for example, may be at increased risk for sickle cell anemia if exposed to carbon monoxide or cyanide. Exposure to lead or benzine can be especially hazardous to the health of people with the thalassemia gene. Presently, few companies report using genetic tests; the tests currently available can identify only a small number of relatively rare diseases, are costly to perform, and difficult to administer. But advances in genetic research and technology, accelerated by the 15-year, $3 billion federally-funded Human Genome Project which aims to decode the genetic makeup of humans, are likely to soon make available simplified, less costly tests able to detect a wide range of common genetic disorders, including those not necessarily associated with worksite exposure, such as predisposition to heart disease, cancer, and manic depression. As such tests become available, it is anticipated that interest in testing will grow.

92. W. Banzhaf, List Of Publications
Back to publications Overview Evolving chess playing programs; Some considerations ofDiversity and Effective Variation Distance in Linear genetic Programming;
http://ls11-www.cs.uni-dortmund.de/people/banzhaf/gp.html
List of Publication Titles in Genetic Programming
Wolfgang Banzhaf
Older papers (from 1993 back) are represented by abstracts only and are available upon email request
We give titles and links. If you click the underlined words in a title you will see an abstract and source information of the paper. If you click the corresponding filename you will retrieve a copy. Back to Publications Overview

93. NSGC - Resources
Resources Find a Counselor; Buy Labels; Bookstore; Job Connection; publications.© 1995 2004 National Society of genetic Counselors, Inc.
http://www.nsgc.org/resources/index.asp
Resources Reference Links Buy Labels Bookstore ... Contact Us Resources
If you have comments about this web site, or if you have found an error, please contact webmaster@nsgc.org
Site design by Professional Web Concepts, Inc

94. Cooperative Human Linkage Center
genetic maps showing the positions of genetic markers. The maps are searchable by name. Includes project information and publications.
http://gai.nci.nih.gov/CHLC/
The Cooperative Human Linkage Center
Maps Markers Publications Information Welcome to the Cooperative Human Linkage Center World Wide Web server. The following information is available: What's New! Last modified: Mon June 07 1999 The Informatics Group (help@chlc.org)

95. NSGC - Publications: Subscription To Perspectives In Genetic Counseling Newslett
Subscription to Perspectives in genetic Counseling Newsletter Perspectivesin genetic Counseling is the quarterly newsletter of the NSGC.
http://www.nsgc.org/resources/pgc_newsletter.asp
Resources Reference Links Buy Labels Bookstore ... Contact Us Subscription to Perspectives in Genetic Counseling Newsletter Perspectives in Genetic Counseling is the quarterly newsletter of the NSGC. In it you will find timely articles about our profession, highlighting actions of the Board of Directors, new legislation regarding genetics issues and genetic counselors, marketing strategies of the organization, what's in the media regarding medical genetics, updates on the activities of the NSGC special interest groups, regions, and committees, and reviews of current resources such as books and videos. There are also announcements of meetings and job listings to help you find that perfect position. Members also write their stories of how they created new positions where none had existed. Sample column titles include:
  • The Creative Job Search The Larger Genetics Community On the Road Media Watch Billing, Licensure and Reimbursement: Success Stories What's on the Web Global Perspective Resources
Subscribers will receive 4 issues: March, June, September and December. Send check for $25 payable to: National Society of Genetic Counselors, Inc. to NSGC, Inc., 233 Canterbury Drive, Wallingford PA 19086-6617. Sorry, credit cards are not accepted at this time.

96. PacNoRGG Publications
As of July 2002, we are no longer distributing hard copies of publications. English(6 pages, 150 KB) Spanish (6 pages, 175 KB) Could it Be genetic?
http://mchneighborhood.ichp.edu/pacnorgg/Publications.htm

PacNoRGG Home
Providence Midwifery Brochures The following are educational materials developed by and made available through the Pacific Northwest Regional Genetics Group (PacNoRGG). Publications can be viewed, printed, or downloaded to your computer using the software Adobe Acrobat. Acrobat is available free of charge from the Adobe Acrobat web site, http://www.adobe.com/prodindex/acrobat/readstep.html
As of July 2002, we are no longer distributing hard copies of publications.
Chromosome Rearrangements Discovered Through Prenatal Diagnosis

Provides families with information about unusual chromosome abnormalities detected by prenatal diagnosis. Discusses inversions, translocations and markers.
English
(6 pages, 150 KB)
Spanish
(6 pages, 175 KB)
Could it Be Genetic?
Outlines indications for referral for pediatric and adult genetic counseling.
English
(2 pages, 75 KB)

97. Genetic Algorithms Publications
genetic Algorithm publications. Confused abouthow to view an article? Click here. Go to
http://www.pitt.edu/~aesmith/genetic.html
Genetic Algorithm Publications
Confused about how to view an article? Click here
Go to:
Journal Articles

98. Apr_Subject
Submission to the Royal Commission on genetic Modification Date of publicationNovember 2000 This is a submission from the Ministry of Health to the Royal
http://www.moh.govt.nz/moh.nsf/0/83d2c9ea036a1179cc2569ec0007069e?OpenDocument

99. Apr_Subject
A Survey of Phenotypic and genetic Methods Used to Identify and DifferentiateThermotolerant Campylobacter spp. strains A Report
http://www.moh.govt.nz/moh.nsf/0/f5e48506f7409b3ecc256af7007cc431?OpenDocument

100. ONS Publications - Position Statements
Cancer Predisposition genetic Testing and Risk Assessment Counseling.The ability to identify individuals who are at increased risk
http://www.ons.org/publications/positions/CancerPredisposition.shtml
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Cancer Predisposition Genetic Testing and Risk Assessment Counseling
The ability to identify individuals who are at increased risk for developing cancer because of an inherited altered (mutated) cancer predisposition gene is possible through cancer predisposition genetic testing. However, while providing the capability to target those individuals who might benefit from specific strategies for medical management of high-risk individuals, genetic testing also raises ethical, legal, and social issues associated with revealing one's genetic makeup. It Is the Position of ONS That
  • Risk assessment counseling and cancer predisposition genetic testing are components of comprehensive cancer care. All healthcare providers offering these services to patients and family members must have educational preparation in both human genetic principles and oncology. Cancer predisposition genetic testing requires informed consent and must include pre- and post-test counseling and follow-up by qualified individuals (e.g., advanced practice oncology nurses or oncologists with specialized education in hereditary cancer genetics, certified genetic counselors with specialized training in oncology).

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