A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.

Author:

Ghaffari S R,Boyd E,Tolmie J L,Crow Y J,Trainer A H,Connor J M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference34 articles.

1. Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease;Lamb, J.; Harris, P.C.; Lindenbaum, R.H.;Lancet,1989

2. Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5;Overhauser, J.; Bengtsson, U.; McMahon, J.,1989

3. Cryptic translocations and telomere integrity;Minireview, Ledbetter D.H.;AmJHum Genet,1992

4. Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms;Wilkie, A.O.M.;Am_J Hum Genet,1993

5. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation;Flint, J.; Wilkie, A.O.M.; Buckle, V.J.; Winter, R.M.; Holland, A.J.; McDermid, H.E.;Nat Genet,1995

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