Results 1 -
7
of
7
for
Partial deletion of the short arm of chromosome 1
- ... generation. A child may inherit a copy of chromosome 11 this is missing a piece of the short arm, which causes WAGR syndrome. 11p deletion syndrome 11p partial monosomy syndrome WAGR complex WAGR contiguous gene syndrome ...
- ... Cri-du-chat syndrome occurs in an estimated 1 in 20,000 to 50,000 newborns. This condition is found in people of all ethnic backgrounds. Cri-du-chat syndrome is caused by a deletion of the end of the short (p) arm of chromosome 5. This chromosomal change is written as 5p-. ...
- ... of Wolf-Hirschhorn syndrome is estimated to be 1 in 50,000 births. However, it is likely ... of the short (p) arm of chromosome 4. This chromosomal change is sometimes written as ...
- ... so the true prevalence may be closer to 1 in 15,000 individuals. In most people with Smith-Magenis syndrome, the condition results from the deletion of a small piece of chromosome 17 in each cell. This deletion occurs on the short (p) arm of the chromosome at a position designated p11. ...
- ... individuals have an unusually small head size (microcephaly). Deletions from the q arm of chromosome 18 occur in an estimated 1 in 55,000 newborns worldwide. Most of these ...
- ... 8 syndrome is caused by a rearrangement of chromosome 8 that results in a deletion of a piece of the short (p) arm and a duplication of a piece of the ...
- ... with Jacobsen syndrome. Jacobsen ... the deletion occurs at the end of the long arm of the chromosome. Less commonly, the deletion occurs ...