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Interpreting Family Histories and Identifying Patients Part 3: Chromosome Anomalies

Interpreting Family Histories and Identifying Patients Part 3: Chromosome Anomalies

Interpreting Family Histories and Identifying Patients Part 3: Chromosome Anomalies

Peter Farndon
Peter Farndon
on behalf of Health Education England

$12.70 $ 12.70 $ 12.70

$ 12.70 $ 12.70 $ 12.70
$ 12.70 $ 12.70 $ 12.70
Normal Price: $12.70 $12.70

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Launch date: 12 Apr 2018
Expiry Date:

Last updated: 29 Apr 2018

Reference: 187961

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Description

This session is one of three sessions that consider the main classes of genetic conditions. Here we cover chromosome anomalies.

Objectives

By the end of this session you will be able to:
• Recognise the types of clinical features that are often associated with changes in the number or structure of chromosomes
• Interpret a family history/family tree for patterns which might suggest an inherited chromosome anomaly
• Describe how genetic probability is estimated for chromosome anomalies
Peter Farndon

Author Information Play Video Bio

Peter Farndon
on behalf of Health Education England

Peter Farndon, Professor of Clinical Genetics and Consultant Clinical Geneticist in Birmingham, has been involved with the practical application of genetics for patients for nearly 25 years. He has had a long standing interest in genetic education, and in 2004 set up the NHS National Genetics Education and Development Centre, leading the team as the Centre’s director. He is a guardian for the RCGP “Genetics in Primary Care” curriculum statement.

His main research interest is in an inherited condition which predisposes to congenital anomalies and skin cancer. He is chair of the UK Genetic Testing Network and is a past President of the Clinical Genetics Society.

Current Accreditations

This course has been certified by or provided by the following Certified Organization/s:

  • Health Education England
  • 0.50 Units -
    Exam Pass Rate: 60

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