Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother, RG Shah… - Journal of Experimental …, 2020 - rupress.org
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome.
A Helfricht, PE Thijssen, MB Rother… - The Journal of …, 2020 - europepmc.org
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
[HTML][HTML] Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother, RG Shah… - Journal of Experimental …, 2020 - rupress.org
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
[PDF][PDF] Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother, RG Shah… - J. Exp …, 2020 - pdfs.semanticscholar.org
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
[PDF][PDF] Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother, RG Shah, L Du… - J. Exp. Med, 2020 - core.ac.uk
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother… - The Journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
[PDF][PDF] Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother, RG Shah, L Du… - J. Exp …, 2020 - scienceopen.com
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, P Thijssen, MB Rother, RG Shah… - The Journal of …, 2020 - repub.eur.nl
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, P Thijssen, M Rother, R Shah… - Journal of Experimental …, 2020 - hal.science
The autosomal recessive immunodeficiency, centromeric instability, and facial anomalies
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
(ICF) syndrome is a genetically heterogeneous disorder. Despite the identification of the …
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
A Helfricht, PE Thijssen, MB Rother, RG Shah… - Journal of Experimental …, 2020 - cir.nii.ac.jp
抄録< jats: p> The autosomal recessive immunodeficiency, centromeric instability, and facial
anomalies (ICF) syndrome is a genetically heterogeneous disorder. Despite the …
anomalies (ICF) syndrome is a genetically heterogeneous disorder. Despite the …