Add to ORKGGenomic imprinting is the parental-allelespecific expression of genes. Beckwith-Wiedemann syndrome (BWS), a congenital overgrowth syndrome with increased risk of childhood tumors, is one of the well-known diseases caused by imprinted genes. The imprinted genes causing BWS are discussed in this review
Genomic imprinting is a remarkable phenomenon through which certain genes show monoallelic expressio...
Beckwith–Wiedemann syndrome (BWS) is a complex imprinting disorder involving fetal overgrowth and pl...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
Genomic imprinting is the parental-allelespecific expression of genes. Beckwith-Wiedemann syndrome (...
This chapter provides a thorough overview of Beckwith-Wiedemann syndrome, which is considered to be ...
Genomic imprinting refers to the parent-of-origin specific monoallelic expression of a gene. Imprin...
Beckwith-Wiedemann Syndrome (BWS) results from mutations or epigenetic events involving imprinted ge...
Beckwith-Wiedemann syndrome (BWS) is the commonest overgrowth cancer predisposition disorder and rep...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
The Beckwith–Wiedemann syndrome (BWS) is geneti-cally linked to chromosome 11p15.5, and a variety of...
The overgrowth disorder Beckwith-Wiedemann syndrome (BWS) is associated with dysregulation of imprin...
A large cluster of imprinted genes is located on the mouse distal chromosome 7. This cluster is well...
The imprinted expression of the IGF2 and H19 genes is controlled by the Imprinting Centre 1 (IC1) at...
Genomic imprinting is an epigenetic phenomenon restricting gene expression in a manner dependent on ...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
Genomic imprinting is a remarkable phenomenon through which certain genes show monoallelic expressio...
Beckwith–Wiedemann syndrome (BWS) is a complex imprinting disorder involving fetal overgrowth and pl...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
Genomic imprinting is the parental-allelespecific expression of genes. Beckwith-Wiedemann syndrome (...
This chapter provides a thorough overview of Beckwith-Wiedemann syndrome, which is considered to be ...
Genomic imprinting refers to the parent-of-origin specific monoallelic expression of a gene. Imprin...
Beckwith-Wiedemann Syndrome (BWS) results from mutations or epigenetic events involving imprinted ge...
Beckwith-Wiedemann syndrome (BWS) is the commonest overgrowth cancer predisposition disorder and rep...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
The Beckwith–Wiedemann syndrome (BWS) is geneti-cally linked to chromosome 11p15.5, and a variety of...
The overgrowth disorder Beckwith-Wiedemann syndrome (BWS) is associated with dysregulation of imprin...
A large cluster of imprinted genes is located on the mouse distal chromosome 7. This cluster is well...
The imprinted expression of the IGF2 and H19 genes is controlled by the Imprinting Centre 1 (IC1) at...
Genomic imprinting is an epigenetic phenomenon restricting gene expression in a manner dependent on ...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
Genomic imprinting is a remarkable phenomenon through which certain genes show monoallelic expressio...
Beckwith–Wiedemann syndrome (BWS) is a complex imprinting disorder involving fetal overgrowth and pl...
The parent of origin-dependent expression of the IGF2 and H19 genes is controlled by the imprinting ...
