Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where the gene is implicated
<div><p>Nijmegen breakage syndrome (NBS) with <i>NBS1</i> germ-line mutation is a human autosomal re...
Nijmegen Breakage Syndrome (NBS) is associated with cancer predisposition, premature aging, immune d...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where t...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by increas...
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
The human genetic disorder, Nijmegen breakage syn-drome (NBS), is characterized by radiosensitivity,...
Abstract: Biallelic mutations in the NBS1 gene are responsible for the Nijmegen breakage syndrome (N...
The Nijmegen breakage syndrome (NBS) is a genetic disorder. caused by mutations in NBN gene and char...
Nijmegen breakage syndrome is a recessive genetic disorder, characterized by elevated sensitivity to...
<div><p>Nijmegen breakage syndrome (NBS) with <i>NBS1</i> germ-line mutation is a human autosomal re...
Nijmegen Breakage Syndrome (NBS) is associated with cancer predisposition, premature aging, immune d...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where t...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by increas...
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
The human genetic disorder, Nijmegen breakage syn-drome (NBS), is characterized by radiosensitivity,...
Abstract: Biallelic mutations in the NBS1 gene are responsible for the Nijmegen breakage syndrome (N...
The Nijmegen breakage syndrome (NBS) is a genetic disorder. caused by mutations in NBN gene and char...
Nijmegen breakage syndrome is a recessive genetic disorder, characterized by elevated sensitivity to...
<div><p>Nijmegen breakage syndrome (NBS) with <i>NBS1</i> germ-line mutation is a human autosomal re...
Nijmegen Breakage Syndrome (NBS) is associated with cancer predisposition, premature aging, immune d...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
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