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pro vyhledávání: '"Claudia Mertel"'
Autor:
Jasmin Beygo, Claudia Mertel, Sabine Kaya, Gabriele Gillessen-Kaesbach, Thomas Eggermann, Bernhard Horsthemke, Karin Buiting
Publikováno v:
Epigenetics, Vol 13, Iss 8, Pp 822-828 (2018)
Temple syndrome (TS14) is a rare imprinting disorder caused by genetic and epigenetic alterations on chromosome 14q32. A subset of these patients shows an imprinting defect (ID) where the paternal allele harbors a maternal epigenotype thus silencing
Externí odkaz:
https://doaj.org/article/2dedb7cd87464bab982259b254e89412
Autor:
Gabriele Gillessen-Kaesbach, Thomas Eggermann, Bernhard Horsthemke, Claudia Mertel, Jasmin Beygo, Sabine Kaya, Karin Buiting
Publikováno v:
Epigenetics. 13:822-828
Temple syndrome (TS14) is a rare imprinting disorder caused by genetic and epigenetic alterations on chromosome 14q32. A subset of these patients shows an imprinting defect (ID) where the paternal allele harbors a maternal epigenotype thus silencing