Crossref
journal-article
Elsevier BV
The Lancet (78)
References
22
Referenced
55
10.1056/NEJM198609043151002
/ N Engl J Med / Preventive screening for the fragile X syndrome by Turner (1986)10.1016/0092-8674(91)90397-H
/ Cell / Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome by Verkerk (1991)10.1126/science.252.5009.1179
/ Science / The fragile X genotype is characterised by an unstable region of DNA by Yu (1991)10.1126/science.252.5009.1097
/ Science / Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome by Oberle (1991)- D. Heitz, F. Rousseau, PCR amplification across the fragile-X mutation, Am J Med Genet (Proceedings of 5th X Linked Mental Retardation Conference, Strasbourg (in press)).
10.1002/ajmg.1320380219
/ Am J Med Genet / Clinical screening score for the fragile X (Martin-Bell) syndrome by Laing (1991)10.1002/ajmg.1320140413
/ Am J Med Genet / The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers by Fishburn (1983)10.1056/NEJM198009183031202
/ N Engl J Med / Heterozygous expression of X-linked mental retardation and the marker X: fra (X) (q27) by Turner (1980)10.1111/j.1469-1809.1984.tb00830.x
/ Hum Genet / The marker X syndrome: a cytogenetic and genetic analysis by Sherman (1984)10.1002/ajmg.1320300164
/ Am J Med Genet / Investigation of the segregation of the fragile X mutation in daughters of obligate carrier women by Sherman (1988)- Mw Partington, H. Robinson, S. Laing, G. Turner, Mortality in the fragile X syndrome, Am J Med Genet ((in press)).
10.1002/ajmg.1320300134
/ Am J Med Genet / Prenatal diagnosis of the fragile X—the Australasian experience by Purvis-Smith (1988)10.1002/ajmg.1320300153
/ Am J Med Genet / A family with the Coffin Lowry syndrome revisited; localisation of CLS to Xp21-pter by Partington (1988)10.1002/ajmg.1320290322
/ Am J Med Genet / Rett syndrome in monozygotic twins by Partington (1988)10.1002/ajmg.1320340402
/ Am J Med Genet / Borjeson-Forssman-Lehmann syndrome: clinical manifestations and gene localization to Xq26-27 by Turner (1989)10.1002/ajmg.1320300125
/ Am J Med Genet / A new syndrome with mental retardation, short stature and an Xq duplication by Thode (1988)10.1002/ajmg.1320300127
/ Am J Med Genet / X-linked mental retardation with dystonic movements of the hands by Partington (1988)10.1111/j.1399-0004.1990.tb03385.x
/ Clin Genet / A new syndrome of familial short stature, small hands, valvular heart disease and a characteristic facies by Collins (1990)10.1002/ajmg.1320400405
/ Am J Med Genet / A new X linked syndrome of mental retardation, gynaecomastica and obesity is linked to DXS255 by Wilson (1991)10.1002/ajmg.1320300151
/ Am J Med Genet / A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14 by Suthers (1988)10.1136/jmg.28.6.372
/ J Med Genet / Localisation of the MRX3 gene for non-specific X-linked mental retardation by Gedeon (1991)- B. Modell, The need for a science of community genetics-lecture, Genetic Services Provision: an International perspective (8th International Congress of Human Genetics, Washington, 1991).
Dates
Type | When |
---|---|
Created | 21 years, 11 months ago (Sept. 22, 2003, 5:55 p.m.) |
Deposited | 4 years, 10 months ago (Oct. 13, 2020, 8:48 a.m.) |
Indexed | 1 day, 10 hours ago (Sept. 2, 2025, 6:36 a.m.) |
Issued | 33 years, 4 months ago (May 1, 1992) |
Published | 33 years, 4 months ago (May 1, 1992) |
Published Print | 33 years, 4 months ago (May 1, 1992) |
@article{Turner_1992, title={Population screening for fragile X}, volume={339}, ISSN={0140-6736}, url={http://dx.doi.org/10.1016/0140-6736(92)91142-u}, DOI={10.1016/0140-6736(92)91142-u}, number={8803}, journal={The Lancet}, publisher={Elsevier BV}, author={Turner, G and Robinson, H and Laing, S and Goddard, A and van den Berk, M and Sherman, S and Colley, A and Partington, M}, year={1992}, month=may, pages={1210–1213} }