Showing posts with label Genetics. Show all posts
Showing posts with label Genetics. Show all posts
05 July 2015

Noonan syndrome ppts and 500 published articles

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What is Noonan syndrome? Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial ch...
16 November 2014

Hypoplasia Ppts and Published articles

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Hypoplasia is underdevelopment or incomplete development of a tissue or organ Optic Nerve Hypoplasia   Julie Greenlee Angela Howe http://www...
22 September 2012

Wolf-Hirschhorn syndrome

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Wolf Hischhorn Chromosome Abnormality Andrew Waters https://sharepoint.cisat.jmu. edu DNA strand, mRNA strand http://www.unity.edu Disease ...
27 July 2012

Noonan syndrome

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Noonan syndrome is a disease that can be passed down through families (inherited). It causes abnormal development in many parts of the body....
15 July 2012

Dyskeratosis congenita

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Dyskeratosis congenita (DC) Philip J Mason http://www.siteman.wustl.edu/ Dyskeratosis congenita Clinical features http://web.campbell.edu/ ...
29 June 2012

Aarskog syndrome

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Aarskog syndrome or Aarskog–Scott syndrome Aarskog syndrome is an inherited disease that affects a person's height, muscles, skeleton, g...
31 May 2012

Apoptosis

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Apoptosis: An overview Sanjeev Sharma*, Aarti Bhardwaj$, Shalini Jain# and Hariom Yadav Apoptosis: An overview .ppt MOLECULAR BIOLOGY OF APO...
28 March 2012

Uniparental disomy Ppt and free 50 published articles

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Uniparental disomy (UPD) occurs when a person receives two copies of a chromosome, or part of a chromosome, from one parent and no copies fr...
29 February 2012

Prenatal Genetic Counseling and Evaluation Ppt

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Prenatal Diagnosis Objectives PrenDxNOTES02.ppt Genetic Counseling Jon  Weil TAGC.ppt Genetic Counseling  for Neurogenetic Condition...
28 February 2012

Fusion proteins Ppt

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Fusion proteins or chimeric proteins are proteins created through the joining of two or more genes which originally coded for separate p...
04 February 2012

Duchenne muscular dystrophy -DMD Ppts and Latest 50 Published artilces

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Duchenne muscular dystrophy is an inherited disorder that involves rapidly worsening muscle weakness. Duchenne muscular dystrophy (DMD) is a...
27 September 2009

Prenatal Testing And Screening

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Prenatal Testing And Screening By:Adel D. Gilbert, MS, CGC Genetic Medicine Education Coordinator Institute of Genetic Medicine Johns Hopkin...
20 May 2009

ADHD and Mental Retardation

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ADHD and Mental Retardation By:Daniel M. Bagner, M.S. Mental Retardation * Sub average intelligence (IQ * Associated adaptive defici...

Genetic Diseases

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Genetic Diseases Presentation by:Amrik Sahota Dept Path & Lab Med UMDNJ - RWJMS What’s the Nature of This Talk? * Review * Previ...

Variations in Chromosome Number and Arrangement

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Variations in Chromosome Number and Arrangement * Chromosomal mutations or aberrations o Abnormal chromosomal number ...

Reasons for Referral to Genetics

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Reasons for Referral to Genetics Prenatal or preconceptional patient who is or will be: * Age 35 years or older at the time of delivery ...

Rates of Autism in Fragile X syndrome

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Rates of Autism in Fragile X syndrome (FXS) FXS OVERVIEW * Fragile X syndrome (FXS), also called Martin-Bell syndrome, is the most commo...

Fragile X Syndrome

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Fragile X Syndrome By: Mary Beth Oliver, Megan Lawrence, Kayla Sink An inherited disorder caused by a defective gene on the X-chromosome an...

Fragile X syndrome

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Fragile X syndrome Defenition: A genetic disorder which can cause cognitive impairment and a number of other physical and behavioural charac...
02 May 2009

Male-Female Binary and Sex Determination

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Male-Female Binary and Sex Determination Gender/Sex/Sexuality Diversity Usual Sex Chromosomes XXXXY Chromosomes More than one X = Barr Bodie...