Introduction and Results Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal recessive disease, characterized by severe hypomethylation in pericentromeric regions of chromosomes (1, 16 and 9), marked immunodeficiency and facial anomalies. The majority of ICF patients present mutations in the DNMT3B gene, affecting the DN
Background: ICF syndrome (standing for Immunodeficiency, Centromere instability and Facial anomalies...
Immunodeficiency, centromeric instability and facial anomalies type I (ICF1) syndrome is a rare gene...
Immunodeficiency with centromeric instability and facial anomalies (ICF) syndrome is a primary immun...
<div><p>Introduction and Results</p><p>Immunodeficiency, centromeric instability and facial anomalie...
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
International audienceBACKGROUND: Immunodeficiency Centromeric Instability and Facial anomalies (ICF...
ICF syndrome is a rare autosomal recessive disease characterized by variable immunodeficiency, centr...
SummaryImmunodeficiency in association with centromere instability of chromosomes 1, 9, and 16 and f...
The recessive autosomal disorder known as ICF syndrome(1-3) (for immunodeficiency, centromere instab...
Item does not contain fulltextBACKGROUND: Immunodeficiency, centromeric instability and facial dysmo...
Abstract The Immunodeficiency, Centromeric region instability, Facial anomalies syndrome (ICF) is a ...
International audienceImmunodeficiency, Centromeric Instability, Facial Anomalies (ICF) syndrome is ...
The life-threatening Immunodeficiency, Centromeric Instability and Facial Anomalies (ICF) syndrome i...
The ICF syndrome is a rare, autosomal recessive disorder, often fatal in childhood, and characterize...
Immunodeficiency, Centromeric Instability, Facial Anomalies (ICF) syndrome is a rare autosomal reces...
Background: ICF syndrome (standing for Immunodeficiency, Centromere instability and Facial anomalies...
Immunodeficiency, centromeric instability and facial anomalies type I (ICF1) syndrome is a rare gene...
Immunodeficiency with centromeric instability and facial anomalies (ICF) syndrome is a primary immun...
<div><p>Introduction and Results</p><p>Immunodeficiency, centromeric instability and facial anomalie...
Immunodeficiency, centromeric instability and facial anomalies syndrome (ICF) is a rare autosomal re...
International audienceBACKGROUND: Immunodeficiency Centromeric Instability and Facial anomalies (ICF...
ICF syndrome is a rare autosomal recessive disease characterized by variable immunodeficiency, centr...
SummaryImmunodeficiency in association with centromere instability of chromosomes 1, 9, and 16 and f...
The recessive autosomal disorder known as ICF syndrome(1-3) (for immunodeficiency, centromere instab...
Item does not contain fulltextBACKGROUND: Immunodeficiency, centromeric instability and facial dysmo...
Abstract The Immunodeficiency, Centromeric region instability, Facial anomalies syndrome (ICF) is a ...
International audienceImmunodeficiency, Centromeric Instability, Facial Anomalies (ICF) syndrome is ...
The life-threatening Immunodeficiency, Centromeric Instability and Facial Anomalies (ICF) syndrome i...
The ICF syndrome is a rare, autosomal recessive disorder, often fatal in childhood, and characterize...
Immunodeficiency, Centromeric Instability, Facial Anomalies (ICF) syndrome is a rare autosomal reces...
Background: ICF syndrome (standing for Immunodeficiency, Centromere instability and Facial anomalies...
Immunodeficiency, centromeric instability and facial anomalies type I (ICF1) syndrome is a rare gene...
Immunodeficiency with centromeric instability and facial anomalies (ICF) syndrome is a primary immun...