AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been identified and sequenced. The protein product of this gene forms a complex with hMre11 and hRad50 – proteins that are involved in repairing double-strand breaks in DNA
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
ow nloaded from 2 The human genetic disorder, Nijmegen Breakage Syndrome (NBS), is characterised by ...
Nijmegen breakage syndrome (NBS) results from the absence of the NBS1 protein, responsible for detec...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
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...
The human genetic disorder, Nijmegen breakage syn-drome (NBS), is characterized by radiosensitivity,...
Nijmegen breakage syndrome is a recessive genetic disorder, characterized by elevated sensitivity to...
The present report deals with the functional relationships among protein complexes which, when mutat...
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
The Nijmegen breakage syndrome (NBS) is a genetic disorder. caused by mutations in NBN gene and char...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
ow nloaded from 2 The human genetic disorder, Nijmegen Breakage Syndrome (NBS), is characterised by ...
Nijmegen breakage syndrome (NBS) results from the absence of the NBS1 protein, responsible for detec...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
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...
The human genetic disorder, Nijmegen breakage syn-drome (NBS), is characterized by radiosensitivity,...
Nijmegen breakage syndrome is a recessive genetic disorder, characterized by elevated sensitivity to...
The present report deals with the functional relationships among protein complexes which, when mutat...
Alterations of the NBS1 gene are responsible for Nijmegen breakage syndrome (NBS), which is characte...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
The Nijmegen breakage syndrome (NBS) is a genetic disorder. caused by mutations in NBN gene and char...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
ow nloaded from 2 The human genetic disorder, Nijmegen Breakage Syndrome (NBS), is characterised by ...
Nijmegen breakage syndrome (NBS) results from the absence of the NBS1 protein, responsible for detec...
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