Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis-Reference-Cited by-同舟云学术

Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis

Published:2016-12 Issue:6 Volume:55 Page:863-866
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Libotte Francesco,Bizzoco Domenico,Gabrielli Ivan,Mesoraca Alvaro,Cignini Pietro,Vitale Salvatore Giovanni,Marilli Ilaria,Gulino Ferdinando Antonio,Rapisarda Agnese Maria Chiara,Giorlandino Claudio

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference17 articles.

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3. Pallister–Killian syndrome;Izumi;Am J Med Gen C Semin Med Genet,2014

4. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister–Killian syndrome phenotype;Vermeesch;Eur J Med Genet,2005

5. The use of interphase for prenatal diagnosis of Pallister–Killian syndrome;Mowery-Rushton;Prenat Diagn,1997

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