Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes’ clinical diagnostics

• Autorzy: Kutkowska-Kazmierczak A. , Niepokoj K. , Wertheim-Tysarowska K. , Giza A. , Mordasewicz-Goliszewska M. , Bal J. , Obersztyn E.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2015
• Tom: 56
• Numer: 3
• Opis fizyczny: p.329–337,fig.,ref.

Twórcy

autor

Kutkowska-Kazmierczak A.

• Department of Medical Genetics, The Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland

autor

Niepokoj K.

• Department of Medical Genetics, The Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland

autor

Wertheim-Tysarowska K.

• Department of Medical Genetics, The Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland

autor

Giza A.

• Department of Medical Genetics, The Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland

autor

Mordasewicz-Goliszewska M.

• One Day Pediatric Department, The Institute of Mother and Child, Warsaw, Poland

autor

Bal J.

• Department of Medical Genetics, The Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland

autor

Obersztyn E.

• Department of Medical Genetics, The Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland

Identyfikatory

DOI

10.1007/s13353-014-0266-1