We describe a family with direct transmission of a duplication of 8p12-->8p21.1. The phenotype of affected realtives included mild mental retardation but no minor anomalies. The duplication was identified by means of GTG-banding and fluorescence in situ hybridization with a probe specific for 8p12 generated by microdissection and degenerate oligonucleotide primed-polymerase chain reaction. Assay of glutathione reductase, which has been localised to 8p21.1, was significantly increased when compared with controls with normal chromosomal constitution. To the best of our knowledge, a proximal direct duplication of 8p restricted to subbands p12-->p21.1 has not been reported so far. The reported aberration is compared with other partial dup...
The 8p23.1 deletion syndrome is established but not an equivalent duplication syndrome. Here, we rep...
Duplications of chromosome region 15q11q13 often occur as a supernumerary chromosome 15. Less freque...
A mentally retarded male with dysmorphic features was found to have a de novo 46,XY,inv dup(8) (p.23...
We describe a family with direct transmission of a duplication of 8p12-->8p21.1. The phenotype of...
We report a family in which six individuals were carriers of a translocation between chromosomes 8 a...
Ten patients with inverted duplication of 8p (inv dup 8p) were studied with cytogenetic, biochemical...
We report on a girl with a de novo inverted duplication of chromosome 8 (q21.2-q22.3) associated wit...
Duplications of distal 8p with and without significant clinical phenotypes have been reported and ar...
We report on the clinical and cytogenetic findings in 7 cases of inverted duplication of region 8p11...
We report on a mother and her two sons who had a direct duplication of chro-mosome region 8p22-8p23....
The 8p23.1 duplication syndrome (8p23.1 DS) is a recurrent genomic condition with an estimated preva...
We report on clinical and cytogenetic data on 5 children and 2 adults with a de novo inverted duplic...
Inversion duplications of the short arm of chromosome 8 (8p) with common morphology have been descr...
Submicroscopic copy-number variations make a considerable contribution to the genetic etiology of hu...
Submicroscopic copy-number variations make a considerable contribution to the genetic etiology of hu...
The 8p23.1 deletion syndrome is established but not an equivalent duplication syndrome. Here, we rep...
Duplications of chromosome region 15q11q13 often occur as a supernumerary chromosome 15. Less freque...
A mentally retarded male with dysmorphic features was found to have a de novo 46,XY,inv dup(8) (p.23...
We describe a family with direct transmission of a duplication of 8p12-->8p21.1. The phenotype of...
We report a family in which six individuals were carriers of a translocation between chromosomes 8 a...
Ten patients with inverted duplication of 8p (inv dup 8p) were studied with cytogenetic, biochemical...
We report on a girl with a de novo inverted duplication of chromosome 8 (q21.2-q22.3) associated wit...
Duplications of distal 8p with and without significant clinical phenotypes have been reported and ar...
We report on the clinical and cytogenetic findings in 7 cases of inverted duplication of region 8p11...
We report on a mother and her two sons who had a direct duplication of chro-mosome region 8p22-8p23....
The 8p23.1 duplication syndrome (8p23.1 DS) is a recurrent genomic condition with an estimated preva...
We report on clinical and cytogenetic data on 5 children and 2 adults with a de novo inverted duplic...
Inversion duplications of the short arm of chromosome 8 (8p) with common morphology have been descr...
Submicroscopic copy-number variations make a considerable contribution to the genetic etiology of hu...
Submicroscopic copy-number variations make a considerable contribution to the genetic etiology of hu...
The 8p23.1 deletion syndrome is established but not an equivalent duplication syndrome. Here, we rep...
Duplications of chromosome region 15q11q13 often occur as a supernumerary chromosome 15. Less freque...
A mentally retarded male with dysmorphic features was found to have a de novo 46,XY,inv dup(8) (p.23...