Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
Fanconi anemia (FA), an autosomal recessive chromosomal instability syndrome, is characterized clini...
The Nijmegen Breakage Syndrome (NBS) is a rare autosomal recessive disorder associated with microce...
Biallelic mutations in the NBN gene are responsible for the Nijmegen breakage syndrome (NBS), a rare...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where t...
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
The Nijmegen Breakage Syndrome (NBS) is a rare chromosomal instability disorder clinically character...
Nijmegen breakage syndrome is a rare autosomal congenital disorder. It originates from mutations in ...
Contains fulltext : 70531.pdf (publisher's version ) (Closed access)Nijmegen break...
Nijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by microcephaly, i...
Genetic heterogeneity in Nijmegen breakage syndrome (NBS) is highlighted by patients showing clinica...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
Fanconi anemia (FA), an autosomal recessive chromosomal instability syndrome, is characterized clini...
The Nijmegen Breakage Syndrome (NBS) is a rare autosomal recessive disorder associated with microce...
Biallelic mutations in the NBN gene are responsible for the Nijmegen breakage syndrome (NBS), a rare...
Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved
Review on NBS1 (Nijmegen breakage syndrome 1), with data on DNA, on the protein encoded, and where t...
SummaryNijmegen breakage syndrome (NBS) is a rare autosomal recessive disorder characterized by micr...
AbstractNijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome ...
AbstractThe gene mutated in Nijmegen breakage syndrome, a chromosome instability disorder, has been ...
The Nijmegen Breakage Syndrome (NBS) is a rare chromosomal instability disorder clinically character...
Nijmegen breakage syndrome is a rare autosomal congenital disorder. It originates from mutations in ...
Contains fulltext : 70531.pdf (publisher's version ) (Closed access)Nijmegen break...
Nijmegen breakage syndrome (NBS) is an autosomal recessive disorder characterized by microcephaly, i...
Genetic heterogeneity in Nijmegen breakage syndrome (NBS) is highlighted by patients showing clinica...
Nijmegen breakage syndrome (NBS) is an autosomal recessive chromosomal instability syndrome characte...
In this work we have studied cells derived from five Italian patients characterised by growth delay,...
Fanconi anemia (FA), an autosomal recessive chromosomal instability syndrome, is characterized clini...
The Nijmegen Breakage Syndrome (NBS) is a rare autosomal recessive disorder associated with microce...
Biallelic mutations in the NBN gene are responsible for the Nijmegen breakage syndrome (NBS), a rare...
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