Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.-Reference-Cited by-同舟云学术

Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.

Published:1995-01-01 Issue:1 Volume:32 Page:68-71
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Horn D,Majewski F,Hildebrandt B,Korner H

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Tetrasomy 12p (Pallister-Killian syndrome);Schinzel, A.;Jf Med Genet,1991

2. Pallister-Killian syndrome in older children and adolescents;Horneff, G.; Majewski, F.; Hildebrand, B.; Voit, T.; Lenard, H.G.;Pediatr Neurol,1993

3. Mosaic tetrasomy 12p;Gilgenkrantz, S.; Droulle, P.; Schweitzer, M.;Clin Genet,1985

4. Pallister-Killian syndrome diagnosed by chorionic villus sampling;Sharland, M.; Hill, L.; Patel, R.; Patton, M.;Prenat Diagn,1991

5. Prenatal diagnosis of tetrasomy 47, XY,+i (12p) confirmed by in situ hybridization;Shivashankar, L.; Whitney, E.; Colmorgen, G.;Prenat Diagn,1988

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