<p>Genome-wide array CGH identified a deletion of approximately 3.5 Mb in individual 1194 (chr4:111,994,000–115,504,000) (red bar). The deletion is located telomeric to the <i>PITX2</i> gene on chromosome 4. The positions of conserved elements (CE) in the deleted region, as identified by Volkmann et al., 2011 [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0153757#pone.0153757.ref047" target="_blank">47</a>] are marked by orange ellipses. Genes transcribed on the forward strand are in blue and those transcribed on the reverse strand are in green, also indicated by arrows. Genomic coordinates are shown on the x-axis and are based on the Human Genome Assembly hg18.</p
<p>All <i>FOXL2</i> encompassing deletions were initially identified using MLPA. The regulatory dele...
<p>The Hox 9-11 paralog regions of the Hoxa (<b>A</b>), Hoxb (<b>B</b>), Hoxc (<b>C</b>), and Hoxd (...
We have sequenced 1949 kb from the terminal Giemsa light band of human chromosome 16p, enabling us t...
Telomerase, a ribonucleoprotein enzyme that maintains telomere length, is crucial for cellular immor...
<p>Overview of the <i>FOXL2</i> region (chr3:135099979–142458004; UCSC, Human Genome Browser, hg19) ...
<p>Arrow heads indicating direction of transcription on reverse strand. Methylation assay locations ...
<p>(A) Schematic representation of ia2 deletion in chromosome 1 (in red). All the STS and genes mapp...
<p>A) Identification of a hemizygous Xq22.1 deletion with a 370 K SNP microarray (Illumina): Y-axes ...
<p>Several annotated genes and ESTs are present, the two deletions are indicated by black arrows (pa...
Conserved genomic sequences disrupted in humans may underlie uniquely human phenotypic traits. We id...
The genome contains the code of life: conservation of DNA sequence ensures proper stereotypical patt...
Background. Isolated growth hormone deficiency (IGHD) and multiple pituitary hormone deficiency (MPH...
<p>Top panel represents chromosome 2p16.1p14 showing the seven male subjects in our study together w...
Conserved genomic sequences disrupted in humans may underlie uniquely human phenotypic traits. We id...
Extensive sequencing in the HoxD complex of several vertebrate species has revealed a set of conserv...
<p>All <i>FOXL2</i> encompassing deletions were initially identified using MLPA. The regulatory dele...
<p>The Hox 9-11 paralog regions of the Hoxa (<b>A</b>), Hoxb (<b>B</b>), Hoxc (<b>C</b>), and Hoxd (...
We have sequenced 1949 kb from the terminal Giemsa light band of human chromosome 16p, enabling us t...
Telomerase, a ribonucleoprotein enzyme that maintains telomere length, is crucial for cellular immor...
<p>Overview of the <i>FOXL2</i> region (chr3:135099979–142458004; UCSC, Human Genome Browser, hg19) ...
<p>Arrow heads indicating direction of transcription on reverse strand. Methylation assay locations ...
<p>(A) Schematic representation of ia2 deletion in chromosome 1 (in red). All the STS and genes mapp...
<p>A) Identification of a hemizygous Xq22.1 deletion with a 370 K SNP microarray (Illumina): Y-axes ...
<p>Several annotated genes and ESTs are present, the two deletions are indicated by black arrows (pa...
Conserved genomic sequences disrupted in humans may underlie uniquely human phenotypic traits. We id...
The genome contains the code of life: conservation of DNA sequence ensures proper stereotypical patt...
Background. Isolated growth hormone deficiency (IGHD) and multiple pituitary hormone deficiency (MPH...
<p>Top panel represents chromosome 2p16.1p14 showing the seven male subjects in our study together w...
Conserved genomic sequences disrupted in humans may underlie uniquely human phenotypic traits. We id...
Extensive sequencing in the HoxD complex of several vertebrate species has revealed a set of conserv...
<p>All <i>FOXL2</i> encompassing deletions were initially identified using MLPA. The regulatory dele...
<p>The Hox 9-11 paralog regions of the Hoxa (<b>A</b>), Hoxb (<b>B</b>), Hoxc (<b>C</b>), and Hoxd (...
We have sequenced 1949 kb from the terminal Giemsa light band of human chromosome 16p, enabling us t...