Considering specific clinical features as evidence of pathogenic copy number variants

• Autorzy: Preiksaitiene E. , Molyte A. , Kasnauskiene J. , Ciuladaite Z. , Utkus A. , Patsalis P. C. , Kucinskas V.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2014
• Tom: 55
• Numer: 2
• Opis fizyczny: p.189-196,fig.,ref.

Twórcy

autor

Preiksaitiene E.

• Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661 Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santariskiu Clinics, Vilnius, Lithuania

autor

Molyte A.

• Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661 Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santariskiu Clinics, Vilnius, Lithuania

autor

Kasnauskiene J.

• Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661 Vilnius, Lithuania

autor

Ciuladaite Z.

• Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661 Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santariskiu Clinics, Vilnius, Lithuania

autor

Utkus A.

• Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661 Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santariskiu Clinics, Vilnius, Lithuania

autor

Patsalis P. C.

• Translational Genetics Team, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus

autor

Kucinskas V.

• Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Santariskiu st. 2, 08661 Vilnius, Lithuania
• Centre for Medical Genetics, Vilnius University Hospital Santariskiu Clinics, Vilnius, Lithuania

Uwagi

Rekord w opracowaniu

Identyfikatory

DOI

10.1007/s13353-014-0197-x