Laurence, J.C. , and Moon, R.C.: Four cases of "retinitis pigmentosa" occurring in the same family and accompanied by general imperfections of development . Ophthalmol. Rev.2: 32, 1866.
2.
Bardet, G.: Sur un syndrome d'obesite congenital avec polydactylie et retinite pigmentaire: contribution a l'etude des formes cliniques de l'obesite hypophysaire . These de Paris No. 470, 1920.
3.
Biedl, A.: Ein Geschwisterpaar mit adiposogenitaler dystrophie. Dtsch. Med. Wochenschr.48: 1630, 1922.
4.
Nadymi, B., Flanagan, M.J., and Christian, J.R.: Laurence-Moon-Biedl syndrome associated with multiple genitourinary tract anomalies. Am. J. Dis. Child.117: 352, 356, 1969.
5.
Klein, D., and Ammann, F.: The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland . J. Neurol. Sci.9: 479, 1969.
6.
Rao, K.S.: The Laurence-Moon-Bardet-Biedl syndrome: report of two cases. Indian Med. Gaz.85: 542, 1950.
7.
Bauman, M.L. , and Hogan, G.R.: Laurence-Moon-Biedl syndrome. Report of two unrelated children less than three years of age. Am. J. Dis. Child.126: 119, 1973.
8.
Cockayne, E.A. , Krestin, D., and Sorsley, A.: Obesity, hypogenitalism, mental retardation, polydactyly, and retinal pigmentation. Q. J. Med.4: 93, 1935.