New developments in the fragile X syndrome.

Author:

Moore D. W.

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference10 articles.

1. Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium;Sutherland, G.R.;Science,1977

2. X Linked mental retardation and the fragile X syndrome: a clinical approach;Frvns, J.P.,1989

3. Identification of a gene FMR-1 containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X svndrome;Verkerk, A.J.; Pieretti, M.; Sutcliffe, J.S.; Fu, Y.-H.; Kuhl, D.P.; Pizzuti, A.;Cell,1991

4. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome;Oberle, I.; Rousseau, F.; Heitz, D.; Kretz, C.; Derys, D.; Hanauer, A.;Science,1991

5. Fragile X genotype characterised by an unstable region of DNA;Yu, S.; Pritchard, E.; Kramer, E.; Lynch, M.; Nancernow, J.; Baker, E.;Science,1991

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1. Perioperative Management of the Mentally and Physically Impaired Patient;Oral and Maxillofacial Surgery Clinics of North America;1999-11

2. Screening for Fragile X Syndrome: Information Needs for Health Planners;Journal of Medical Screening;1997-06

3. Carirer diagnosis of the fragile X syndrome—A challenge in antenatal clinics;American Journal of Obstetrics and Gynecology;1995-04

4. Fragile X (Martin-Bell) syndrome;Special Care in Dentistry;1994-01

5. The Fragile-X Syndrome and Adoption;Adoption & Fostering;1993-10

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