Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations

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概要

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2011-03-01

著者

Hadzsiev Kinga
Department Of Medical Genetics And Child Development University Of Pecs
Kosztolanyi Gyorgy
Department Of Medical Genetics And Child Development University Of Pecs
Melegh Bela
Department of Medical Genetics and Child Development
Hadzsiev Kinga
Department Of Medical Genetics Faculty Of Medicine University Of Pecs
POLGAR Noemi
Department of Medical Genetics, Faculty of Medicine, University of Pecs
BENE Judit
Department of Medical Genetics, Faculty of Medicine, University of Pecs
KOMLOSI Katalin
Department of Medical Genetics, Faculty of Medicine, University of Pecs
KARTESZI Judit
Department of Medical Genetics, Faculty of Medicine, University of Pecs
HOLLODY Katalin
Department of Pediatrics, University of Pecs
RENIERI Alessandra
Department of Molecular Biology, Medical Genetics Unit, University of Siena
Bene Judit
Department Of Medical Genetics Faculty Of Medicine University Of Pecs
Polgar Noemi
Department Of Medical Genetics Faculty Of Medicine University Of Pecs
Karteszi Judit
Department Of Medical Genetics Faculty Of Medicine University Of Pecs
Hollody Katalin
Department Of Pediatrics University Of Pecs
Komlosi Katalin
Department Of Medical Genetics Faculty Of Medicine University Of Pecs
Renieri Alessandra
Department Of Molecular Biology Medical Genetics Unit University Of Siena
Melegh Bela
Department Of Medical Genetics Faculty Of Medicine University Of Pecs

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