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Judit Balog

Showing results (31-40 of 38) with videos related to

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Plos Genetics|July 14, 2009
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD)Weihua Zeng, Jessica C de Greef, Yen-Yun Chen, et al.
Journal of Medical Genetics|November 3, 2019
Intronic <i>SMCHD1</i> variants in FSHD: testing the potential for CRISPR-Cas9 genome editingRemko Goossens, Marlinde L van den Boogaard, Richard J L F Lemmers, et al.
Journal of Medical Genetics|March 23, 2018
Monosomy 18p is a risk factor for facioscapulohumeral dystrophyJudit Balog, Remko Goossens, Richard J L F Lemmers, et al.
Human Molecular Genetics|September 27, 2014
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, et al.
Brain : a Journal of Neurology|September 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophyRichard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, et al.
American Journal of Human Genetics|May 21, 2011
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2Jessica C de Greef, Jun Wang, Judit Balog, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral DystrophyMarlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Plos Genetics|July 14, 2009
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD)Weihua Zeng, Jessica C de Greef, Yen-Yun Chen, et al.
Journal of Medical Genetics|November 3, 2019
Intronic <i>SMCHD1</i> variants in FSHD: testing the potential for CRISPR-Cas9 genome editingRemko Goossens, Marlinde L van den Boogaard, Richard J L F Lemmers, et al.
Journal of Medical Genetics|March 23, 2018
Monosomy 18p is a risk factor for facioscapulohumeral dystrophyJudit Balog, Remko Goossens, Richard J L F Lemmers, et al.
Human Molecular Genetics|September 27, 2014
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2Richard J L F Lemmers, Jelle J Goeman, Patrick J van der Vliet, et al.
Brain : a Journal of Neurology|September 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophyRichard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, et al.
American Journal of Human Genetics|May 21, 2011
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2Jessica C de Greef, Jun Wang, Judit Balog, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral DystrophyMarlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Pageof 4