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Oxford handbook of genetics [E-book]

By: Language: English Series: Oxford medical handbooksPublication details: Oxford : Oxford University Press, 2010Description: 1 online resource (xxix, 449 p.)ISBN:
  • 9780199598922
  • 9780199545360
Subject(s): NLM classification:
  • QZ 39
Online resources: Summary: (electronic resource)Summary: This handbook provides accessible information on specific genetic diseases, and possible genetic components of major diseases, for the primary health care team and junior doctor in training. It assists with why, when, and where to refer patients, and affected families, to get the best advice about genetic disease.
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Item type Home library Class number Status Date due Barcode
Electronic book BEH-MHT Library Service On website Available STOCKYLOQ0
Electronic book CEME Library (NELFT) On website Available
Electronic book Croydon Health Services Library On website Available
Electronic book David Adams Library (Royal Marsden) On website Available
Electronic book Ferriman information and Library Service (North Middlesex) On website Available
Electronic book Lewisham and Greenwich NHS Trust Library On website Available
Electronic book Newham Library (Barts Health) Online Available
Electronic book Oxleas NHS Foundation Trust Knowledge Services On website Available
Electronic book PRUH Education Centre Library On website Available
Electronic book Royal London Library (Barts Health) Online Available
Electronic book South London and Maudsley Trust Library On website Available
Electronic book St Bartholomew's Library (Barts Health) Online Available
Electronic book Stenhouse Library On website Available
Electronic book Whipps Cross Library (Barts Health) Online Available
Electronic book Whittington Health Library On website eBook (Browse shelf(Opens below)) Available

Includes index.

(electronic resource)

This handbook provides accessible information on specific genetic diseases, and possible genetic components of major diseases, for the primary health care team and junior doctor in training. It assists with why, when, and where to refer patients, and affected families, to get the best advice about genetic disease.

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