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  • The Honeybush Miracle.
    Perhaps a little eclipsed by the world-wide success of Rooibos, another natural South African health tea, Honeybush; is finally getting the attention it deserves.

    Honeybush tea ( botanical name: Cyclopia intermedia ) grows along mountain slopes in the Cedarberg and Langkloof area, and has a naturally sweet, almost honey-like taste. Its brewing colour is a pinky red. South Africa produces only 200 tons of Honeybush tea per year. Not much when compared to the annual Rooibos tea crop of around 4000 tons. This lesser known tea has, however, apparently plenty to offer.

    Just like the ever popu ...
    Author: Janet Holmes
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    Today's Featured Articles:

  • Slaying The Green Eyed Monster

    He hasn't called in hours. You call and get the roommate: "Oh, sorry ....he got in really late last night and is still asleep!"

    Your mind starts racing: "What did he do last night?" Your heart starts to pound. You feel sick to your stomach.. Uh, oh... you're jealous. You feel like you can't live with yourself one more minute until you find out what is going on ... suddenly, the potential threat to the relationship becomes the most important thing in the world ... more important than eating, working or concentrating on tasks at hand. More important than ... living life itself.

    Ac ...
    Author: Sam Stevens
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  • LED Photo Rejuvenation/Intense Pulsed Light/Infra-Red Light Affects Skin Rejuvenation

    LED Photo Rejuvenation,Intense Pulsed Light or Infra-Red Light and it’s Affects on Skin Rejuvenation

    In order for your skin to continue to exist, it has to constantly reproduce new cells to take the place of the ones that are being shed.

    People need certain wavelengths of light similar to the way plants need sunlight to thrive. Your skin has the ability to absorb light and use it as a source of energy to stimulate cellular regeneration.

    LED Photo Rejuvenation or Intense Pulsed Light (P.R./IPL) is infra-red light which stimulates the cell activity; this increases Collagen a ...
    Author: Nancy LaTouche
    CLICK HERE TO READ THE REST OF THIS ARTICLE

    Want to read more of our articles?  Check out the Archive.

    Article Archive: Pages 1 2 3 4 5 6 7 8 9 10 11 12 13

     

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    Genetics News:

    Ring Chromosome 20 Syndrome With Intractable Epilepsy
    Ring chromosome 20 syndrome is characterized by mild to moderate learning disability*, behavioural disorders, epilepsy, and various dysmorphic features.


    Rubinstein-Taybi Syndrome
    Rubinstein-Taybi syndrome is characterized by distinctive facial features, mental retardation, and broad great toes and thumbs. Research has found a genetic error on chromosome 16 in about 20% of individuals with the syndrome....


    Angelman Syndrome
    Angelman syndrome, caused by a genetic defect on chromosome 15, includes developmental delay, near absence of speech, and facial abnormalities. The most striking characteristic of someone with Angelman syndrome, though, is the appearance of being happy most of the time,...


    Angelman Syndrome
    Angelman syndrome (pronounced "angleman"), caused by a genetic defect on chromosome 15, includes developmental delay, near absence of speech, and facial abnormalities. The most striking characteristic of someone with Angelman syndrome, though, is the appearance of being happy most of...


    Bowel-bypass syndrome without bowel bypass. Bowel-associated dermatosis-arthritis syndrome
    JL Jorizzo, P Apisararax, P Subrt, AA Hebert, … - Arch I Med, 1983 - ncbi.nlm.nih.gov ... Bowel-associated dermatosis-arthritis syndrome. ... We propose the expanded term,bowel-associated dermatosis-arthritis syndrome, to incorporate these new cases. ...::


     

     
     


  • New Hope for Chronic Fatigue and Fibromyalgia Sufferers

    There are numerous theories with regard to the causes of chronic fatigue and fibromyalgia, many of which may be indeed touching on the truth or at least touching on an aggravator or contributor to these afflictions. Diseases in general have been growing in epidemic proportion over at least the past 20 years, especially in the United States, where our increasingly toxic environment and lifestyles have drifted further and further away from what is natural in the name of progress, technology, and profit. Chronic fatigue and fibromyalgia are no exception, the two often being experienced togethe ...
    Author: Deb Bromley
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    Here are a few more sites I've chosen if you'd like to read more and do more research:

  • Genetic and Rare Diseases Information Center - Office of Rare Diseases
    ... Chromosome 3, Trisomy 3q2 Chromosome 4 ring syndrome Chromosome 4 short arm deletion Chromosome 4 ... ... 4, partial trisomy distal 4q Chromosome 4, Trisomy 4p Chromosome 4, trisomy 4q Chromosome 4 ...


  • http://www.genetichealthvic.net.au/pages/links.html
    ... 11Q Network Chromosome 18 Home Page Chromosome 22 Central Coffin-Lowry Syndrome Foundation ... ... Syndrome Association Williams Syndrome Foundation Wolf-Hirshhorn (4p-)Parent Contact Group WAGR ...


  • President Abraham Lincoln: Health & Medical History
    ... regurgitation or Marfan syndrome. Third, Lincoln was ... House, as was the embalming [4p]. Odds & Ends [Top] In ... has been traced to a gene on chromosome 11. Lincoln was not one of ...


  • Basic genetics for the clinical neurologist -- Placzek and Warner 73 (Supple...
    ... If a recessive allele is present on the X chromosome in a domain that is not present on the Y ... ... and Becker muscular dystrophy and fragile X syndrome. Mitochondria are inherited matrilineally ...


  • Abstract index
    ... of 1p34-36 in three cases with myelodysplastic syndrome and characterisation by FISH K.A. Rack , S ... ... S. Bizic 2.90 Dicentric chromosome 9 in an ALL case who had t(4p;9p) G. Durakbasi , C. Ucar ...


  • 1996 Centromere/Telomere Meeting Abstracts
    ... individual with Li-Fraumeni Syndrome. ALT was also detected in ... of the FSHD region on human chromosome 4qter: Sequence homology ... with the subtelomeric region of 4p Jane E Hewitt 1, Morag C ...


  • Wolf-Hirschhorn syndrome
    ... nih.gov ... This ancillary meeting, entitled "Recent Research on Chromosome 4p Syndromes andGenes," reviewed the history of the Wolf-Hirschhorn syndrome (WHS), the ...... The detection of subtelomeric ...


  • Wolf Hirschhorn Syndrome - Quest Diagnostics Patient Health Library
    ... 4, Partial Deletion 4p Partial Deletion of the Short Arm of Chromosome 4 Chromosome 4, Partial Monosomy 4p 4p- Syndrome, Partial Disorder Subdivisions None General Discussion Wolf-Hirschhorn ...


  • ABNORMALITIES IN CHROMOSOME STRUCTURE
    ... This can be terminal (close to the end of the chromosome on the long arm or the short arm), or it can ... ... of an individual) include Wolf-Hirschhorn syndrome (4p-), and cri-du-chat syndrome (5p-). They ...


  • Endotext.com - Obesity, Ch 8 Bibliography
    ... A, Robinson H, Turner G 1991 New X-linked syndrome of mental retardation, gynecomastia, and ... ... quantitative-trait locus for obesity on chromosome 4p in Mexican Americans. Am J Hum Genet. 74 ...


  • http://www.openwindow.com/ftp/genles.fls
    ... lung, breast and other cancers A72=chromosome 17p Q73= Congenital%Wolf-Hirschorn syndrome A73=syndrome: prominent forehead and nasal root^genetics: deletion 4p Q74= Congenital%Cri-du-chat syndrome ...


  • Wolf-Hirschhorn Syndrome
    You are here: About>Health & Fitness>Rare / Orphan Diseases> Information by Disease Type> Chromosome Disorders> Wolf-Hirschhorn Syndrome Health & Fitness Rare Diseases Essentials Rare ...


  • Genetic Bank - E. O. Ospedali Galliera
    ... SUPERnumerary marker chromosome 5 supernumerary marker ... marker YOUNG-SIMPSON SYNDROME _ By Genotype gene PS1 : R ... 21p) 46,XX,del(2q37) 46,XX,del(4p)(p15.2-->(pter) 46,XX,del(7q ...


  • Chromosome 4p- syndrome
    ... Espanol Enter the name or the first few letters of the article: Or click on the first letter of the article: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Chromosome 4p- syndrome Chromosome 4p ...


  • TheFetus.net - Case of the week #162-Fabrice Cuillier, MD
    ... by Cuillier 46XX/47XY + 22 mosaicism-HTML 4p- syndrome -HTML Absence of fibula type II -HTML ... ... Chondrodysplasia punctata, rhizomelic-HTML Chromosome 15 ring, 46XX,r(15)-HTML Cleft lip ...


  • MUMS: List of Disorders - Chromosomes
    ... p23.1-) Translocation (1) Chromosome 4p+;9q- Unbalanced Translocation (1) Chromosome 4p- & Chromosome 21 Translocation (1) * Chromosome 4p- & Triple X (1) Chromosome 4p- (Wolf-Hirschhorn Syndrome) (33 ...


  • : The AMEDEO Literature Guide
    ... EEG patterns in Wolf-Hirschhorn (4p-) syndrome. Brain Dev 2005;27 ... available AICARDI J Aicardi syndrome. Brain Dev 2005;27:164-71 ... clinical phenotypes of chromosome disorders associated with ...


  • Institut für Humangenetik der Universität Erlangen - Nürnberg
    ... A (2002) Partial deletion of 4p and 4q in a fetus with ring ... large family supporting the chromosome 15q13-22 locus. Mol ... and Nijmegen breakage syndrome homozygotes and ...


  • Genetic Conditions & Support Groups | The Association of Genetic Support...
    ... 18 Registry & Research Society (Aust), The Chromosome Disorders - rare Cleft Pals, The Cleft ... ... Aldrich syndrome Wolf-Hirschhorn syndrome Wolf-Hirschhorn 4p- Syndrome Support Group Wolff ...


  • Noah's Never Ending Rainbow - A National Trisomy Organization
    ... syndrome, Trisomy 18, Trisomy 13, 11q, Trisomy 9, 4p-, cri-du-chat , deletions, inversions ... ... ring, sex-chromosome anomalies , mosaicisms, fragile-x syndrome, other trisomy ...


  • Craniofacial Center | Dallas, Texas
    ... in a gene FGFR3 on chromosome 4p. Currently, no one knows what causes this mutation to occur. Typically, both the mother and father of a child born with Crouzon syndrome have normal genes, and ...


  • chromosome groups
    ... an American website, has been set up for families of individuals with chromosome 2q abnormalities. Wolf-Hirschhorn (4p-) Syndrome, a German page - with English text too and links to other (European ...


  • ORPHANET® : Base de données sur les maladies rares et les m&eacut...
    ... stature Thrombocytopenia chromosome breakage Thrombocytopenia ... A syndrome Triple H (HHH) syndrome Triploidy Trismus ... 3q Trisomy 3q13 2 q25 Trisomy 4p Trisomy 4q Trisomy 4q21 Trisomy ...


  • Syndrome, chromosome 4p- definition - Medical Dictionary definitions of popu...
    About Us | Privacy Policy MedicineNet Home > MedTerms medical dictionary A-Z List > Syndrome, chromosome 4p- search help Printer-Friendly Format | Email to a Friend Definition of Syndrome ...


  • http://www.medschool.umaryland.edu/BTBank/ListofDisorders.htm
    ... Disorder, 46, XX, 5q+ 1 Chromosomal Disorder, 4p-Syndrome 1 Chromosomal Disorder, Balanced Translocation 6,11 1 Chromosomal Disorder, Chromosome 21 Rearrangement 1 Chromosomal Disorder, Deletion ...


  • The DNA sequence of the human X chromosome : Nature
    ... the VCX gene. Also, some instances of Hunter syndrome (OMIM 309900), red-green colour blindness ... ... of approximately 20 Mb at the end of chicken chromosome 4p (Fig. 3a). In contrast, most of the short ...


  • Medical Transcription Resources and Medical Books at BooksForMTs - Medical T...
    http://www.booksformts.com/medterms_sTEXT.html


  • Central Manchester & Manchester Childrens University Hospital
    ... dystrophies Wolf Hirschhorn (4p-) syndrome Cri du Chat (5p ... syndrome Rubenstein Taybi syndrome The diagnostic potential of ... of prenatal diagnosis of chromosome abnormality. In cases with ...


  • Neurosciences u676 - welcome
    ... phenotype with a subtelomeric 4p trisomy. Am J Med Genet A. 2004 ... A. New autosomal recessive syndrome with short stature and facio ... and identifies linkage to chromosome 19q13Circulation. 2004 May ...


  • Cacophobia -
    ... trisomy Chromosome 3 Chromosome 3 duplication syndrome Chromosome 3, monosomy 3p Chromosome 3 ... ... 4, partial trisomy distal 4q Chromosome 4, Trisomy 4p Chromosome 4, trisomy 4q Chromosome 4 ...


  • http://www.esoterik-kraemer.de/27273-Chromosome10pterminaldeletionsyndrome/
    ... syndrome (WHS) is due to a deletion in the terminal ... 4p-supportgroup.org More useful Links Chromosome 10p Terminal Deletion Syndrome Chromosome 10p Terminal Deletion Syndrome Chromosome 10p ...


  • Why Are Antioxidants Important To Me?

    Did you know that when we breath oxygen, it interacts with certain molecules in our bodies to create free radicals and that these free radicals damage important cellular structures such as DNA and cell membranes? Well, it is true and this damage may cause cells to function poorly and mutate. Free radical damage may lead to disease and aging.

    We are exposed to huge amounts of free radicals from pollution, and pesticides. Every time you breathe, you take in millions of free radical molecules created by cigarette smoke, radiation, and automobile emissions. Every time you eat, you consume ...
    Author: Scarlet S. Paolicchi
    CLICK HERE TO READ THE REST OF THIS ARTICLE

     

  • Benefits of Green Tea
    Tea and Cancer Prevention
    Tea drinking is an ancient tradition dating back 5,000 years in China and India. Long regarded in those cultures as an aid to good health, researchers now are studying tea for possible use in the prevention and treatment of a variety of cancers. Investigators are especially interested in the antioxidants-called catechins-found in tea.

    1. What are antioxidants?

    The human body constantly produces unstable molecules called oxidants, also commonly referred to as free radicals. To become stable, oxidants steal electrons from other molecules and, in the p ...
    Author:
    Robert Rogers
    CLICK HERE TO READ THE REST OF THIS ARTICLE

     

     

     

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