Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques.

Author:

Qumsiyeh M B,Tomasi A,Taslimi M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Centric fission in man and other mammals;Imai, H.T.,1988

2. Phenotypekaryotype correlations in dup( 18q): report of a case and review;Am Med Genet,1985

3. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases;Reynolds, J.F.; Daniel, A.; Kelly, T.A.;Anm 7 Med Genet,1987

4. Determining the origin of human X isochromosome by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences;Callen, D.F.; Mulley, J.C.; Baker, E.G.; Sutherland, G.R.;Hum Genet,1987

5. The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in 9 cases by in situ hybridization;Callen, D.F.; Freemantle, C.J.; Ringenbergs, M.L.;Am JtHum Genet,1990

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