Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome

• Autorzy: Tumiene B. , Ciuladaite Z. , Preiksaitiene E. , Mameniskiene R. , Utkus A. , Kucinskas V.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2017
• Tom: 58
• Numer: 4
• Opis fizyczny: p.467-474,fig.,ref.

Twórcy

autor

Tumiene B.

• Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Santariskiu 2, 08661, Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania

autor

Ciuladaite Z.

• Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Santariskiu 2, 08661, Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania

autor

Preiksaitiene E.

• Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Santariskiu 2, 08661, Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania

autor

Mameniskiene R.

• Clinic of Neurology and Neurosurgery, Vilnius University, Vilnius, Lithuania

autor

Utkus A.

• Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Santariskiu 2, 08661, Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania

autor

Kucinskas V.

• Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Santariskiu 2, 08661, Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania

Identyfikatory

DOI

10.1007/s13353-017-0408-3