Novel 1q22-q23.1 duplication in a patient with lambdoid and metopic craniosynostosis, muscular hypotonia, and psychomotor retardation

• Autorzy: Sowinska-Seidler A. , Olech E.M. , Socha M. , Larysz D. , Jamsheer A.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2018
• Tom: 59
• Numer: 3
• Opis fizyczny: p.281–289,fig.,ref.

Twórcy

autor

Sowinska-Seidler A.

• Department of Medical Genetics, Poznan University of Medical Sciences, Rokietnicka 8 Street, 60-806 Poznan, Poland

autor

Olech E.M.

• Department of Medical Genetics, Poznan University of Medical Sciences, Rokietnicka 8 Street, 60-806 Poznan, Poland

autor

Socha M.

• Department of Medical Genetics, Poznan University of Medical Sciences, Rokietnicka 8 Street, 60-806 Poznan, Poland

autor

Larysz D.

• Department of Radiotherapy, The Maria Skłodowska Curie Memorial Cancer Centre and Institute of Oncology, Gliwice Branch, 44-101 Gliwice, Poland

autor

Jamsheer A.

• Department of Medical Genetics, Poznan University of Medical Sciences, Rokietnicka 8 Street, 60-806 Poznan, Poland

Identyfikatory

DOI

10.1007/s13353-018-0447-4