Genetic disorder

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21FAQ:  G6S diagnostic testing Q: What is G6S, and why should I test for it? Caprine Mucopolysaccharideosis-IIID is a lysosomal storage disorder, caused by a genetic mutation (a point mutation)

FAQ: G6S diagnostic testing Q: What is G6S, and why should I test for it? Caprine Mucopolysaccharideosis-IIID is a lysosomal storage disorder, caused by a genetic mutation (a point mutation)

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Source URL: tvmdl.tamu.edu

Language: English - Date: 2015-06-23 16:22:51
    22MY Y STORY Alyssa Clason I have Prader Willi Syndrome, a genetic disorder where I am always hungry and tend to overeat. In 2012 I went to Pittsburgh Children’s Institute Prader Willi Center for a 12-week program in whi

    MY Y STORY Alyssa Clason I have Prader Willi Syndrome, a genetic disorder where I am always hungry and tend to overeat. In 2012 I went to Pittsburgh Children’s Institute Prader Willi Center for a 12-week program in whi

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    Source URL: www.sidney-ymca.org

    - Date: 2014-12-10 08:55:05
      23“Harvey was born with a genetic metabolic condition called peroxome biogenesis disorder. And no, I’d never heard of it either until the doctors broke the news to my wife Lyn and I. Once we’d got past all the fancy

      “Harvey was born with a genetic metabolic condition called peroxome biogenesis disorder. And no, I’d never heard of it either until the doctors broke the news to my wife Lyn and I. Once we’d got past all the fancy

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      Source URL: www.claire-house.org.uk

      Language: English - Date: 2015-04-30 09:23:16
      24MUCOPOLYSACCHARIDOSES  Rare Diseases Unit of the Finnish Association of People with Physical Disabilities  Support for this guide was provided by Genzyme.

      MUCOPOLYSACCHARIDOSES Rare Diseases Unit of the Finnish Association of People with Physical Disabilities Support for this guide was provided by Genzyme.

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      Source URL: www.invalidiliitto.fi

      Language: English - Date: 2015-07-19 05:13:47
      25Investigating the Genetic Basis of Immune-Mediated Hemolytic Anemia in Dogs Owner Consent Form Purpose of Study Immune-mediated hemolytic anemia (IMHA) is common disorder of the immune system in dogs. The immune system a

      Investigating the Genetic Basis of Immune-Mediated Hemolytic Anemia in Dogs Owner Consent Form Purpose of Study Immune-mediated hemolytic anemia (IMHA) is common disorder of the immune system in dogs. The immune system a

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      Source URL: www.ncstatevets.org

      Language: English - Date: 2014-01-13 15:21:27
        26Health Supervision for Children With Down Syndrome Marilyn J. Bull and the Committee on Genetics Pediatrics 2011;128;393; originally published online July 25, 2011; DOI: pedsThe online version of this

        Health Supervision for Children With Down Syndrome Marilyn J. Bull and the Committee on Genetics Pediatrics 2011;128;393; originally published online July 25, 2011; DOI: pedsThe online version of this

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        Source URL: www.dsagc.com

        Language: English - Date: 2014-01-14 15:17:48
        27Newsletter  September 2012 SYSCILIA Newsletter 7 – September 2012 Midterm Review

        Newsletter September 2012 SYSCILIA Newsletter 7 – September 2012 Midterm Review

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        Source URL: syscilia.org

        Language: English - Date: 2012-10-15 08:29:34
        28Human Genetics: Pedigrees  Ch. 14 Name _____________________________ Period _____ COOK Pedigree charts help scientists understand the genetic patterns of diseases. It is important to be able to interpret

        Human Genetics: Pedigrees Ch. 14 Name _____________________________ Period _____ COOK Pedigree charts help scientists understand the genetic patterns of diseases. It is important to be able to interpret

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        Source URL: flashesbiology.weebly.com

        Language: English - Date: 2015-02-16 10:31:44
        29GENETIC TESTING IN INSURANCE AND EMPLOYMENT: A New Form of Discrimination Developments in genetics mean that there will be increasing numbers of tests to detect

        GENETIC TESTING IN INSURANCE AND EMPLOYMENT: A New Form of Discrimination Developments in genetics mean that there will be increasing numbers of tests to detect

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        Source URL: genewatch.org

        Language: English - Date: 2007-05-15 08:10:03
        30Rare diseases / Medical genetics / Cystic fibrosis / Genetic disorder / Disease / Orphan drug / Race and health / Health / Medicine / Epidemiology

        The Rare Disease Taskforce: Key priorities of the National rare Disease Plan. Presentation to the joint Oireachtas Committee on Health. Philip Watt: Chairperson Rare Disease Taskforce; Chairperson MRCG and CEO of Cystic

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        Source URL: www.oireachtas.ie

        Language: English - Date: 2014-07-30 06:18:37