Lymphocyte cultures from five patients with Werner's syndrome (WS) and five healthy controls revealed significantly slower proliferation kinetics in four out of five patients. Higher frequencies of chromosome aberration and aneuploidy were also present with evidence of variegated translocation mosaicism in one of the patients. the study revealed no differences in sister chromatid exchange frequencies.ESCOLA PAULISTA MED,DISCIPLINA GENET,RUA BOTUCATU 740,BR-04023062 São Paulo,BRAZILESCOLA PAULISTA MED,DISCIPLINA GENET,RUA BOTUCATU 740,BR-04023062 São Paulo,BRAZILWeb of Scienc
Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations...
Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations...
markably, centenarian studies revealed WRN and LMNA polymorphic variants among those who have escape...
Werner syndrome is a rare, autosomal, recessive condition that is frequently studied as a model of s...
Werner’s syndrome (WS) and Bloom’s syndrome (BS) are rare autosomal genetic diseases that predispose...
Werner's syndrome is commonly regarded as a model for the study of premature aging. There are, howev...
Werner’s syndrome (WS) is an autosomal recessive disorder displaying many features consistent with a...
A case of Werner's Syndrome in a 47-year-old man, with typical features of pangeria associated with ...
We have determined the mitotic stability of micro- and mini-satellite DNA sequences in SV40-immortal...
Werner syndrome (WS) is an autosomal recessive progeroid disorder caused by mutations in the WRN gen...
The International Registry of Werner syndrome ( www.wernersyndrome.org ) has been providing molecula...
Werner's syndrome (WS) is a rare autosomal recessive human disorder and the patients exhibit many sy...
Werner syndrome (WS) is a premature aging syndrome caused by mutations of the WRN gene. Here, we dem...
Werner syndrome (WS) is a premature aging syndrome caused by mutations of the WRN gene. Here, we dem...
Werner syndrome (WS) is an autosomal recessive disorder characterized by the early onset of several ...
Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations...
Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations...
markably, centenarian studies revealed WRN and LMNA polymorphic variants among those who have escape...
Werner syndrome is a rare, autosomal, recessive condition that is frequently studied as a model of s...
Werner’s syndrome (WS) and Bloom’s syndrome (BS) are rare autosomal genetic diseases that predispose...
Werner's syndrome is commonly regarded as a model for the study of premature aging. There are, howev...
Werner’s syndrome (WS) is an autosomal recessive disorder displaying many features consistent with a...
A case of Werner's Syndrome in a 47-year-old man, with typical features of pangeria associated with ...
We have determined the mitotic stability of micro- and mini-satellite DNA sequences in SV40-immortal...
Werner syndrome (WS) is an autosomal recessive progeroid disorder caused by mutations in the WRN gen...
The International Registry of Werner syndrome ( www.wernersyndrome.org ) has been providing molecula...
Werner's syndrome (WS) is a rare autosomal recessive human disorder and the patients exhibit many sy...
Werner syndrome (WS) is a premature aging syndrome caused by mutations of the WRN gene. Here, we dem...
Werner syndrome (WS) is a premature aging syndrome caused by mutations of the WRN gene. Here, we dem...
Werner syndrome (WS) is an autosomal recessive disorder characterized by the early onset of several ...
Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations...
Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by null mutations...
markably, centenarian studies revealed WRN and LMNA polymorphic variants among those who have escape...