The Resource Translocational applications of cardiovascular genomics : opportunities and challenges, Aroon Hingorani, (electronic resource)

Translocational applications of cardiovascular genomics : opportunities and challenges, Aroon Hingorani, (electronic resource)

Label
Translocational applications of cardiovascular genomics : opportunities and challenges
Title
Translocational applications of cardiovascular genomics
Title remainder
opportunities and challenges
Statement of responsibility
Aroon Hingorani
Title variation
Mendelian randomisation to explore causality
Creator
Speaker
Subject
Language
eng
Member of
Cataloging source
UkLU-K
Characteristic
representational
Series statement
Genetics of cardiovascular disease : genetic interactions in a multifactorial disease,
Label
Translocational applications of cardiovascular genomics : opportunities and challenges, Aroon Hingorani, (electronic resource)
Publication
Note
  • Animated audio-visual presentation with synchronized narration
  • Title from title frames
http://library.link/vocab/branchCode
  • net
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Configuration of playback channels
monaural
Content category
two-dimensional moving image
Content type code
tdi
Content type MARC source
rdaconent
Contents
Contents: Ischaemic heart disease -- Valvular heart disease -- Heart muscle disease -- Monogenic form of common disorder -- Single gene disorders and cardiovascular disease -- Mutation both necessary and sufficient to lead to disease -- Genetic basis of the common form of CHD -- Polygenic form of common disorder -- Complex disorders -- Study design -- Candidate genes or whole genome -- Genome-wide association studies -- A new dawn for genetics of complex disorders and traits -- Relationship between allele frequency and effect size -- Genetic architecture of common disease -- Translation of genomic discoveries -- Potential advantages of genetic tests -- Predictive genetic screening for CHD -- Low penetrance polymorphisms -- Multiple risk alleles -- Why genetic testing might perform poorly as a discriminatory test -- Genotype and prediction of CHD -- Using genotype to gain insight into the causes of CHD -- Unique properties of genotype
Control code
HST2178_1_2
Dimensions
unknown
Extent
1 online resource (1 streaming video file (33 min.)
File format
one file format
Governing access note
Access restricted to subscribers
Media category
  • video
  • computer
Media MARC source
  • rdamedia
  • rdamedia
Media type code
  • v
  • c
Medium for sound
other
Other physical details
color, sound)
Publisher number
2178
http://library.link/vocab/recordID
.b37239193
Sound
sound
Sound on medium or separate
sound on medium
Specific material designation
  • remote
  • other
System control number
  • HST217812
  • (UkLU-K)000947309
System details
  • Mode of access: World Wide Web
  • System requirements: Browser compatibility: updated Mozilla Firefox, Google Chrome, Safari or Internet Explorer 8+. Browser settings: enable JavaScript, enable cookies from the Henry Stewart Talks site. Required Desktop Browser plugins & viewers: Updated Adobe Flash Player & Adobe Acrobat Reader. Mobile device & operating system versions: Android v4.0+, iPhone 4+ (iOS v6.x+), iPad 2+ (iOS v6.x+), BlackBerry OS v7.0+, Windows Phone v6.5.1+
Video recording format
other

Library Locations

    • Deakin University Library - Geelong Waurn Ponds CampusBorrow it
      75 Pigdons Road, Waurn Ponds, Victoria, 3216, AU
      -38.195656 144.304955
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