Delay in diagnosis of homocystinuria: retrospective study of consecutive patients

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Title:	Delay in diagnosis of homocystinuria: retrospective study of consecutive patients
Author(s):	Cruysberg, J.R.M. ; Boers, G.H.J. ; Trijbels, J.M.F. ; Deutman, A.F.
Publication year:	1996
Source:	Bmj. British Medical Journal (Compact Ed.), vol. 313, (1996), pp. 1037-1040
ISSN:	0959-535X
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/141861
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Subject:	Dislocated lenses and congenital cataract Enzymatic and molecular genetic defects causing hyperhomocysteinemia Hyperhomocysteinemia: diagnosis and treatment of mild abnormalities. Hyperhomocysteinemia: diagnosis and treatment (till October 1, 1996) Ectopia lentis en vroegtijdig cataract Enzymatische en moleculair genetische defecten als oorzaak voor hyperhomocysteinemia Hyperhomocysteinemie: diagnose en behandeling van milde vormen Hyperhomocysteinemie: diagnostiek en behandeling (tot 1 oktober 1996)
Organization:	Ophthalmology Internal Medicine Paediatrics
Journal title:	Bmj. British Medical Journal (Compact Ed.)
Volume:	vol. 313
Page start:	p. 1037
Page end:	p. 1040