National Institutes of Health
Nih News Release: Marfan Syndrome Research
Article describes characteristics of Marfan Syndrome and reviews research project involving mice with mutant fibrillin gene.
University of Utah
University of Utah: Learn Genetics: Space Doctor
Enter the Extraterrestrial Gene Therapy Lab to test your knowledge of gene therapy when you treat three ailing aliens who have genetic disorders.
US National Library of Medicine
Medline Plus: Cri Du Chat Syndrome
This site has information on causes, symptoms, treatment, support groups, expectations and prognosis related to Cri-du-Chat, a genetic syndrome. Information is objectively presented and fairly thorough. Information is provided by A.D.A.M.
National Institutes of Health
Genes and Disease: Marfan Syndrome
Site specifies genetic cause of Marfan Syndrome as well as gene locus. Also includes disease characteristics and information regarding treatment of cardiovascular symptoms.
University of Arizona
The Biology Project: Human Biology: New Methods for Karyotyping
Read about the findings from the scientific group from the National Center for Human Genome Research, which published a modification to traditional karyotyping that permits rapid identification of chromosomal alterations.
University of Washington
University of Washington Pku Clinic: What Is Pku?
This is a brief article that talks about the causes and effects of phenylketonuria (PKU). Read about how a "normal" person's system converts phenylalanine into tyrosine and how those with phenylketonuria cannot carryout this process.
PBS
Pbs: Our Genes/our Choices: The Probabilities of Problems: A Look at Inheritance
Learn how the genes inherited from two parents can be recombined in their offspring in this simulation activity. In addition, investigate the probabilities of passing on inherited genetic disorders.
University of Michigan
University of Michigan Health System: Your Child: Xxx Syndrome (Trisomy X)
Fact page describes the genetic disorder Triple X Syndrome or Trisomy X. Includes explanation of the genetics involved as well as treatment of the disorder.
University of Arizona
Ua: Diagnosis of Klinefelter's Syndrome
Brief tutorial dealing with Klinefelter's diagnosis. Provides illustration of nondisjunction and Klinefelter's karyotype. Information provided regarding other sex chromosome aneuploidies.
Wikimedia
Wikipedia: Klinefelter's Syndrome
Wikipedia entry for Klinefelter's Syndrome in both mammals and adults. Links are also given for additional information on related subjects.
WebMD
Medicine Net: Genetic Disorder Information on Achondroplasia
Authored by doctors, read this comprehensive overview of Achondroplasia including description, causes, symptoms, diagnosis, treatment, prognosis, prevention, genetic implications to dwarfism.
Other
Sickle Cell Anemia Association: Sickle Cell Anemia
The Sickle Cell Anemia Association invites you to "visit often to get the latest news and available information" on sickle cell anemia. Visit the FAQ section for quick facts and answers to basic questions.
Other
Klinefelter Organisation: About Ks
Excellent review of basic genetics and a description of Klinefelter's Syndrome.
Science Daily
Science Daily: Iowa Researchers Rare, Accelerated Aging Condition
Article summarizes recent University of Iowa research. Progeria patients show deficiencies in certain antioxidant enzymes. Author provides information about possible application of gene therapy in future progeria research and treatment
National Health Museum
Access Excellence: Inheritance of Hemophilia
This site explains the X-linked inheritance of Hemophilia and includes a diagram.
Other
All Things Kabuki: Kabuki Syndrome
This site contains thorough information on Kabuki Syndrome, a rare genetic chromosomal disorder. The table of contents begins with facts about Kabuki Syndrome and contains excellent information on Kabuki. Also available in Italiano.
Curated OER
Kids Health: Turner Syndrome
Turner Syndrome affects about 1 in every 2000 females. This can cause many of the changes that take place during puberty to not develop. This article focuses on the effects of Turner Syndrome and how people live with the disorder. Links...
National Institutes of Health
U.s. National Library of Medicine: Genetic Conditions: Huntington Disease
This resource provides a summary of the disease effects on the body and the genetics behind its inheritance. There are several links to other useful sites.
National Institutes of Health
U.s. National Library of Medicine: Genetics Home Reference: Triple X Syndrome
Fact page describes Triple X Syndrome or Trisomy X. Includes explanation of the genetics involved and treatment of the disorder.
CK-12 Foundation
Ck 12: Life Science: Chromosomal Disorders
[Free Registration/Login may be required to access all resource tools.] Some children are born with genetic defects that are not carried by a single gene. Instead, an error in a larger part of the chromosome or even in an entire...
Other
Dr. Greene's House Calls: Trisomy 13
Doctor describes Trisomy 13 in layperson's terms. Explanations of chromosome 13 function, abnormalities resulting from trisomy, history of syndrome, and prenatal testing.
WebMD
Web Md: Klinefelter's Syndrome
This site from WebMD Health is a very informative approach to klinefelter's syndrome. It has a fairly in-depth topic overview, then discusses symptoms, exams, treatment, home care and other places to get help.
University of Utah
University of Utah: learn.genetics: Finding a Gene on the Chromosome Map
Play the role of a scientist and piece together the genetic puzzle to determine the gene responsible for a disorder.