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Chromosomal Disorders:     more detail

Cytogenetic & Molecular Analysis of Chromosomal Rearrangements Associated With Neuropsychiatric Disorders (Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, 1091) by Dmitry Tentler, 2001-12 Chromosomal abnormalities: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Michelle, MS, CGC Bosworth, 2005 New Chromosomal Syndromes (Chromosomes in biology and medicine) by Yunis, 1977-06 Sex differentiation and chromosomal abnormalities (Birth defects original article series) Musculoskeletal Disorders: Icd-10 Chapter Xvii: Congenital Malformations, Deformations and Chromosomal Abnormalities Chromosomal deletion more common in prison population.(Forensic Psychiatry): An article from: Clinical Psychiatry News by Joyce Frieden, 2005-03-01 Chromosomal abnormalities: An entry from Thomson Gale's <i>Gale Encyclopedia of Science, 3rd ed.</i> by Antonio Farina, Brenda Wilmoth Lerner, et all 2004 Data Book of Chromosomal Test in Vitro by Motoi Ishidate, 1988-04

lists with details

81. CHROMOSOMAL And TERATOLOGIC DISORDERS
    chromosomal and TERATOLOGIC disorders. There are seven major disorders listedin this category. A brief description of each is given in the ensuing text  
    http://www.worldortho.com/database/etext/chromosomal.html

82. Buy The Research Report "The Complete Directory For Pediatric Buy The Research R
    Human Karyotypes Exhibiting Various Abnormalities Normal Male Karyotype Normal Female Karyotype Example of a Down Syndrome Karyotype Example of a Klinefelter Syndrome Karyotype Example of a Turner Syndrome Karyotype  
    http://redirect-west.inktomi.com/click?u=http://www.findmarketresearch.com/marke

83. References
    Karyotyping and chromosomal diseases. Basrur, PK, Kanagawa, H. and Gilman,JPW, 1970. An update of chromosomal abnormalities in mares.  
    http://www.vgl.ucdavis.edu/~lvmillon/refs8.html
    
    Extractions: [This collection of references on genetics of horses is not comprehensive, but should provide good starting material for people looking for information about genetics of horses.] Basrur, P.K., Kanagawa, H. and Gilman, J.P.W., 1970. Further studies on the cell populations of an intersex horse. Journal of Comparative Medicine 34:294-298. Blue, M.G., 1981. A cytogenetical study of prenatal loss in the mare. Theriogenology 15:295-309. Bowling, A.T. and Millon, L., 1988. Centric fission in the karyotype of a mother-daughter pair of donkeys (Equus asinus). Cytogenetics and Cell Genetics 47:152-154. Bowling, A.T. and Millon, L., 1990. Two autosomal trisomies in the horse: 64,XX,-26+t(26q26q) and 65,XX,+30. Genome 33:679-682. Bowling, A.T., Millon, L. and Hughes, J.P., 1987. An update of chromosomal abnormalities in mares. Journal of Reproduction and Fertility, Suppl. 35:149-155. Buckland, R.A., Fletcher, J.M. and Chandley, A.C., 1976. Characterization of the domestic horse

84. Florida State University College Of Medicine Digital Library
    Access document; Nontraditional Inheritance Access document; ChromosomalDisorders Access document; Mitochondrial DNA Abnormalities  
    http://fsumed-dl.slis.ua.edu/clinical/genetics/general.htm
    
    Extractions: Clinical Resources by Topic: Genetic Disorders General Genetic Disorders Clinical Resources Clinical Guidelines Clinical Trials News Miscellaneous Resources See also: Regulation of Gene Expression: Access document Cloning and Sequencing DNA: Access document DNA Sequencing: Access document Status of DNA Sequencing: Access document Ethical Issues: Access document Transmission of Genetic Disease: Access document Genotype and Phenotype: Access document Alleles, Genotypes, and Haplotypes:

85. Exploring Genes & Genetic Disorders
    churning out an unprecedented volume of data on human chromosomes and the tens ofthousands of genes residing on them, many associated with genetic disorders.  
    http://www.ornl.gov/hgmis/posters/chromosome/
    
    Extractions: The U.S. Department of Energy Biological and Environmental Research program funds this site. DOWNLOAD: Gene Gateway Handout (PDF) S cientists, enabled by the Human Genome Project , are churning out an unprecedented volume of data on human chromosomes and the tens of thousands of genes residing on them, many associated with genetic disorders. These data, and many Web sites on human genetic disorders, are freely accessible on the Internet. Listed below are guides and tutorials that provide a gateway for the novice or layperson to find and use this growing wealth of information. Information furnished by resources described in this guide should not be used as a substitute for consultation with a physician. Questions or concerns regarding a medical condition should be discussed with a professional, such as a physician, genetic counselor, or medical geneticist. For more information on genetic health professionals, see the HGPI Genetic Counseling page and the Genetic Health Professionals section of the Genetic Disorder Guide Human Genome Landmarks wall poster depicting the 24 human chromosomes and some g enes associated with disorders and traits. To order a free copy

86. What Causes Language Disorders
    n Recessive patterns of inheritance. n Affected gene unknown. Prevention of ChromosomalDisorders. w Genetic counseling. w Family planning. w Prenatal diagnosis.  
    http://www.southalabama.edu/speechandhearing/431causes.htm

87. Sex Chromosomal Aneuploidies (SCA) - Lucile Packard Children's Hospital
    Sex chromosomal Aneuploidies (SCA). What are Sex chromosomal Aneuploidies?Sex chromosome aneuploidies (SCA) describe those conditions  
    http://www.lpch.org/clinicalSpecialtiesServices/COE/BrainBehavior/Psychiatry/sca
    
    Extractions: Trisomy 21 (Down Syndrome) What are Sex Chromosomal Aneuploidies? Sex chromosome aneuploidies (SCA) describe those conditions in which there is some variation among the normal euploidic sex chromosomes in male (XY) or female (XX) individuals. These variations are most often caused by non-disjunction of the 23rd sex chromosome pair during meiosis. Found in 1 in 400 live newborns, SCA are even more common than Down syndrome or fragile X syndrome. While SCA can include a variety of abnormalities of the sex chromosomes, by far the most commonly occurring SCA involve the deletion (45,X or partial X monosomy) or addition (47,XXY, 47,XYY, 47,XXX) of an X or Y chromosome. Of these conditions, only Turner syndrome, caused by the loss of all or part of an X chromosome, results in an easily identifiable physical phenotype. Subtle language, neuromotor, and learning difficulties have been identified in most forms of SCA, however. The neurodevelopmental effects of the 47XXY (Klinefelter syndrome) and 47XXX karyotypes are also investigated in light of these phenotypic features. Why do we study SCA?

88. Topica Email List Directory
    Click Here! List Directory, Lists Help. Category  
    http://www.topica.com/dir/?cid=2952

89. Topica Email List Directory
    Click Here! List Directory,  
    http://www.topica.com/lists/mosaictrisomy8/?cid=2952

90. Links
    Chromosome Deletion and Epilepsy Links. Parentto-Parent Support Groups,Chromosome Disorder and Random Associated Links, Email Groups.  
    http://chromosome3.virtualave.net/chromeplinks.htm
    
    Extractions: Parent-to-Parent Support Groups Chromosome Disorder and Random Associated Links Email Groups MUMS Parent to Parent Network Chromosomal Deletion Outreach (CDO) UNIQUE: Rare Chromosomal Disorders Support Group Parent to Parent New Zealand ... Alliance of Genetic Support Groups Diagnosis-Matching Internet Bulletin Boards Special Child Parent-to-Parent Matching Bulletin Board Family Village Parent to Parent Web Boards ParentSoup Kids with Special Needs Board Developmental Disabilities Forum ... Medscape Pharmacotherapy Home Page Epilepsy Links Epilepsy in Young Children Epilepsy in Young Children Egroup Parents' Epilepsy Support Group Parents' Epilepsy Support Group Yahoo site ... ParentsPlace Epilepsy Board CaringParents - This list is for adults to discuss the issue of children coping with illness (their own illness, or someone they care about). To subscribe send an e-mail message to: listserv@maelstrom.stjohns.edu

91. Human Diseases
    This is a small and incomplete list of pages related to specific genetic and inheriteddiseases Support groups for families of those affected are included  
    http://www.hgmp.mrc.ac.uk/GenomeWeb/diseases.html
    
    Extractions: This is a small and incomplete list of pages related to specific genetic and inherited diseases Support groups for families of those affected are included where they are known. Notice to members of the public searching for information on inherited diseases: The HGMP-RC provides a service to researchers working on the Human Genome Project, but we are not the most appropriate people to ask about specific genetic diseases. We advise you to find a national support group for the disease and contact them. They will be in touch with people who are directly working on the causes and cures of this disease and will usually have a regular newsletter that you can subscribe to. Your family medical practitioner or your local public library would be a good place to start in contacting the support groups. You should also search the OMIM and GDB databases. Places to start searching

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