'Single gene disorders' diaporamas de présentation

Medical Genetics

Medical Genetics. Instructor: Prof. Dr. Fadel A. Sharif. Contact. Medical Laboratory Sciences University Clinic-Genetics Diagnosis lab fsharif@iugaza.edu. Course Syllabus. - Text: Thompson & Thompson Genetics in Medicine, 7 th Ed., Nussbaum, McInnes, Willard, 2007. Saunders (Required)

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? ????? ? Medical Genetics

? ????? ? Medical Genetics. ??? E-mail: zhangxianning@zju.edu.cn Tel? 13105819271; 88208367 Office: A709, Research Building 2011/02. Nussbaum RL, et al. ??? , ? . Thompson & Thompson Genetics in Medicine, 7th ed. ?????????????? , 2009. Suggested Readings.

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Medical Genetics

Medical Genetics. Fadel A. Sharif. Contact details. Medical Laboratory Sciences Genetics Diagnosis lab fsharif@iugaza.edu. Grades First and Second Hour Exams 40% Final exam 60%. Topics. 1: Patterns of Single-Gene Inheritance 2: Genetic Variation in Individuals

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Therapy of Genetic Disorders MGL-14 May. 6 th 2015

Therapy of Genetic Disorders MGL-14 May. 6 th 2015. Mohammed El-Khateeb. GENE THERAPY. Replacement Therapy Gene transfer Gene manipulation Cloning Stem cell. GENE. Gene Product. Metabolic Functional Structural Effect Effect Effect.

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HUMAN GENETICS

HUMAN GENETICS. Genetic disorders- common cause of diseases, prolonged handicap and death in human. 1% newborns have monogenic diseases like CF, SCD etc. 0.5% have chr . disorders like Down Synd. 1-3% have multifactorial disorders like CHD,

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GENETICS an Introduction

GENETICS an Introduction. SDK. Lecture Road Map. Introduction of the course Details of teaching tools Lectures Group activities and Seminars Evaluation Plan Genetics introduction and clinical examples. Genetic Course.

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Holoproesencephaly

Holoproesencephaly. Holoprosencephaly. First described in 1963 Failure of proper formation of the midline structures of the forebrain is the common feature of the many variant forms. Occurs in about 1/10,000 liveborn infants but is much more frequent in prenatal studies. Etiology of HPE.

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Single Gene Disorders: Molecular Pathology, Prevalence and Diagnosis

Single Gene Disorders: Molecular Pathology, Prevalence and Diagnosis. Dr Maha Al- Sulaimani Department of Biochemistry College of Sciences. Single Gene Disorders.

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The Unique Network Supporting families affected by Rare Chromosome Disorders

The Unique Network Supporting families affected by Rare Chromosome Disorders . Why we are here today. To tell you a little bit about the charity Unique, and how we joined What challenges families affected by a rare chromosome face How Unique helps families

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Biotechnology

Biotechnology. Goal 3.04: Genomics, Human Genome Project, and Applications of Biotechnology. Biotechnology. Using living organisms to perform a process, or modify an existing product/ Practical Applications: Genetic/Paternity Testing Medical (Gene Therapy, Pharmaceuticals)

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A Simple Question

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Genetic Disorders

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Smith- Lemli - Opitz syndrome

Smith- Lemli - Opitz syndrome . By Fiona Schaeffer . You need to know for this Power Point:. This Bullet point means take note of this This bullet point means you do not need to take note of this.

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The Clinic for Special Children

The Clinic for Special Children. Where compassion, care, and bioinformatics result in cutting edge translational medicine .

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