Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features

Author:

Estop A M,Mowery-Rushton P A,Cieply K M,Kochmar S J,Sherer C R,Clemens M,Surti U,McPherson E

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. 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.;Am Hum Genet,1989

2. Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4;Altherr, M.R.; Bengtsson, U.; Elder, F.F.B.;Am _7 Hum Genet,1991

3. Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization;Kuwano, A.; Ledbetter, S.A.; Dobyns, W.B.; Emanuel, B.S.; Ledbetter, D.H.;Am Hum Genet,1991

4. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization;Mewar, R.; Kline, A.D.; Jackson, L.; Overhauser, J.;Am J Med Genet,1992

5. Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring;Alvarado, M.; Bass, H.N.; Caldwell, S.;Am J Dis Child,1993

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