Add to ORKGDNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis, and immune functio
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
The recessive autosomal disorder known as ICF syndrome(1-3) (for immunodeficiency, centromere instab...
Introduction and Results Immunodeficiency, centromeric instability and facial anomalies syndrome (IC...
ICF syndrome is a rare autosomal recessive disease characterized by variable immunodeficiency, centr...
The correct establishment and maintenance of DNA methylation patterns are critical for mammalian dev...
Item does not contain fulltextICF (immunodeficiency, centromeric region instability and facial anoma...
Immunodeficiency, centromeric region instability, cacial anomalies (IcF; OMIM #242860) syndrome, due...
ICF syndrome (immunodeficiency, centromere instability and facial anomalies) is a recessive human ge...
International audienceICF syndrome is a rare autosomal recessive disorder that is characterized by I...
Deficiency in DNA methyltransferase DNMT3B causes a recessive human disorder characterized by immuno...
Immunodeficiency, centromeric instability and facial anomalies type I (ICF1) syndrome is a rare gene...
DNA methyltransferase 3B (DNMT3B) is the major DNMT that methylates mammalian genomes during early d...
International audienceImmunodeficiency, Centromeric Instability, Facial Anomalies (ICF) syndrome is ...
Immunodeficiency, Centromeric region instability, Facial anomalies (ICF; OMIM #242860) syndrome, due...
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
The recessive autosomal disorder known as ICF syndrome(1-3) (for immunodeficiency, centromere instab...
Introduction and Results Immunodeficiency, centromeric instability and facial anomalies syndrome (IC...
ICF syndrome is a rare autosomal recessive disease characterized by variable immunodeficiency, centr...
The correct establishment and maintenance of DNA methylation patterns are critical for mammalian dev...
Item does not contain fulltextICF (immunodeficiency, centromeric region instability and facial anoma...
Immunodeficiency, centromeric region instability, cacial anomalies (IcF; OMIM #242860) syndrome, due...
ICF syndrome (immunodeficiency, centromere instability and facial anomalies) is a recessive human ge...
International audienceICF syndrome is a rare autosomal recessive disorder that is characterized by I...
Deficiency in DNA methyltransferase DNMT3B causes a recessive human disorder characterized by immuno...
Immunodeficiency, centromeric instability and facial anomalies type I (ICF1) syndrome is a rare gene...
DNA methyltransferase 3B (DNMT3B) is the major DNMT that methylates mammalian genomes during early d...
International audienceImmunodeficiency, Centromeric Instability, Facial Anomalies (ICF) syndrome is ...
Immunodeficiency, Centromeric region instability, Facial anomalies (ICF; OMIM #242860) syndrome, due...
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
The recessive autosomal disorder known as ICF syndrome(1-3) (for immunodeficiency, centromere instab...
Introduction and Results Immunodeficiency, centromeric instability and facial anomalies syndrome (IC...