http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
A practical guide to the clinical assessment and investigation of obesity -- Human leptin and leptin receptor deficiency -- Pro-opiomelanocortin deficiency -- Prohormone convertase 1 -- Human melanocortin 4 receptor deficiency -- Albrights hereditary osteodystrophy, pseudoparathyroidism and other GNAS-associated syndromes -- The clinical and molecular genetics of Alström syndrome -- The clinical, molecular and functional genetics of Bardet-Biedl syndrome -- The Börjeson-Forssman-Lehmann syndrome -- Cohen syndrome -- Prader-Willi syndrome -- Syndromes with obesity.
edited by Philip L. Beales, I. Sadaf Farooqi, Stephen O'Rahilly.
Includes bibliographical references and index.
Oxford monographs on medical genetics ; no. 56
Oxford monographs on medical genetics ; 56