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Developmental delay with hypotrophy associated with homozygous functionally relevant REV3L variant.
Halas, Agnieszka; Fijak-Moskal, Jolanta; Kuberska, Renata; Murcia Pienkowski, Victor; Kaniak-Golik, Aneta; Pollak, Agnieszka; Poznanski, Jaroslaw; Rydzanicz, Malgorzata; Bik-Multanowski, Miroslaw; Sledziewska-Gojska, Ewa; Ploski, Rafal.
Afiliación
  • Halas A; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106, Warsaw, Poland.
  • Fijak-Moskal J; Department of Medical Genetics, Jagiellonian University Medical College, 30-663, Krakow, Poland.
  • Kuberska R; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106, Warsaw, Poland.
  • Murcia Pienkowski V; Department of Medical Genetics, Medical University of Warsaw, 02-106, Warsaw, Poland.
  • Kaniak-Golik A; Ardigen, Podole 76, 30-394, Krakow, Poland.
  • Pollak A; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106, Warsaw, Poland.
  • Poznanski J; Department of Medical Genetics, Medical University of Warsaw, 02-106, Warsaw, Poland.
  • Rydzanicz M; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106, Warsaw, Poland.
  • Bik-Multanowski M; Department of Medical Genetics, Medical University of Warsaw, 02-106, Warsaw, Poland.
  • Sledziewska-Gojska E; Department of Medical Genetics, Jagiellonian University Medical College, 30-663, Krakow, Poland.
  • Ploski R; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02-106, Warsaw, Poland. esg@IBB.waw.pl.
J Mol Med (Berl) ; 99(3): 415-423, 2021 03.
Article en En | MEDLINE | ID: mdl-33474647

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Síndromes Neoplásicos Hereditarios / Discapacidades del Desarrollo / Mutación Puntual / Mutación Missense / Proteínas de Unión al ADN / ADN Polimerasa Dirigida por ADN / Neoplasias Primarias Múltiples / Nevo Pigmentado Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Mol Med (Berl) Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Síndromes Neoplásicos Hereditarios / Discapacidades del Desarrollo / Mutación Puntual / Mutación Missense / Proteínas de Unión al ADN / ADN Polimerasa Dirigida por ADN / Neoplasias Primarias Múltiples / Nevo Pigmentado Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Mol Med (Berl) Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2021 Tipo del documento: Article