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  2. Details for: Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.
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Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2. [electronic resource]

By:
  • van den Boogaard, M L
Contributor(s):
  • Thijssen, P E
  • Aytekin, C
  • Licciardi, F
  • Kıykım, A A
  • Spossito, L
  • Dalm, V A S H
  • Driessen, G J
  • Kersseboom, R
  • de Vries, F
  • van Ostaijen-Ten Dam, M M
  • Ikinciogullari, A
  • Dogu, F
  • Oleastro, M
  • Bailardo, E
  • Daxinger, L
  • Nain, E
  • Baris, S
  • van Tol, M J D
  • Weemaes, C
  • van der Maarel, S M
Producer: 20180516Description: 380-387 p. digitalISSN:
  • 1399-0004
Subject(s):
  • Adolescent
  • Adult
  • Animals
  • Centromere -- genetics
  • Child
  • Child, Preschool
  • DNA (Cytosine-5-)-Methyltransferases -- genetics
  • DNA Helicases -- genetics
  • DNA Methylation -- genetics
  • Face -- abnormalities
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Immunologic Deficiency Syndromes -- genetics
  • Male
  • Mice
  • Mutation, Missense
  • Nuclear Proteins -- genetics
  • Repressor Proteins -- genetics
  • Sexism
  • Young Adult
  • DNA Methyltransferase 3B
Online resources:
  • Available from publisher's website
In: Clinical genetics vol. 92
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Publication Type: Journal Article

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Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.

APA

van den Boogaard M. L., Thijssen P. E., Aytekin C., Licciardi F., Kıykım A. A., Spossito L., Dalm V. A. S. H., Driessen G. J., Kersseboom R., de Vries F., van Ostaijen-Ten Dam M. M., Ikinciogullari A., Dogu F., Oleastro M., Bailardo E., Daxinger L., Nain E., Baris S., van Tol M. J. D., Weemaes C. & van der Maarel S. M. (20180516). Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2. : Clinical genetics.

Chicago

van den Boogaard M L, Thijssen P E, Aytekin C, Licciardi F, Kıykım A A, Spossito L, Dalm V A S H, Driessen G J, Kersseboom R, de Vries F, van Ostaijen-Ten Dam M M, Ikinciogullari A, Dogu F, Oleastro M, Bailardo E, Daxinger L, Nain E, Baris S, van Tol M J D, Weemaes C and van der Maarel S M. 20180516. Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2. : Clinical genetics.

Harvard

van den Boogaard M. L., Thijssen P. E., Aytekin C., Licciardi F., Kıykım A. A., Spossito L., Dalm V. A. S. H., Driessen G. J., Kersseboom R., de Vries F., van Ostaijen-Ten Dam M. M., Ikinciogullari A., Dogu F., Oleastro M., Bailardo E., Daxinger L., Nain E., Baris S., van Tol M. J. D., Weemaes C. and van der Maarel S. M. (20180516). Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2. : Clinical genetics.

MLA

van den Boogaard M L, Thijssen P E, Aytekin C, Licciardi F, Kıykım A A, Spossito L, Dalm V A S H, Driessen G J, Kersseboom R, de Vries F, van Ostaijen-Ten Dam M M, Ikinciogullari A, Dogu F, Oleastro M, Bailardo E, Daxinger L, Nain E, Baris S, van Tol M J D, Weemaes C and van der Maarel S M. Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2. : Clinical genetics. 20180516.

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