PROBE FOR DETECTION OF THE FRAGILE X SYNDROME

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EP 0 441 821 A1

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(43)	Date of publication:
	21.08.1991 Bulletin 1991/34

(21)	Application number: 89912003.0

(22)	Date of filing: 01.11.1989

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International Patent Classification (IPC):

G01N 33/ 53^{( . )}
A61K 51/ 00^{( . )}
C07K 16/ 18^{( . )}
C12N 15/ 09^{( . )}
C12Q 1/ 68^{( . )}
G01N 33/ 68^{( . )}

A61K 49/ 00^{( . )}
C07K 14/ 47^{( . )}
C12N 5/ 10^{( . )}
C12P 21/ 08^{( . )}
G01N 33/ 577^{( . )}
C12R 1/ 91^{( . )}

(86)	International application number:
	PCT/GB1989/001303

(87)	International publication number:
	WO 1990/005194 (17.05.1990 Gazette 1990/11)

(84)	Designated Contracting States:
	AT BE CH DE FR GB IT LI LU NL SE

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Priority:

01.11.1988 GB 19880025530

(71)	Applicant: MEDICAL RESEARCH COUNCIL
	London W1N 4AL (GB)

(72)	Inventors:
	DAVIES, Kay, Elizabeth Molecular Genetics Group Hospital Headington Oxford OX3 9DU (GB) BELL, Martin Molecular Genetics Group Hospital Headington Oxford OX3 9DU (GB) PATTERSON, M. Stanford University Medical Centre Stanford, CA 94305-5306 (US)

(74)	Representative: Cresswell, Thomas Anthony, et al
	J.A. KEMP & CO. 14 South Square Gray's Inn London WC1R 5LX London WC1R 5LX (GB)

(54)	PROBE FOR DETECTION OF THE FRAGILE X SYNDROME