Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 23 for Partial deletion of the short arm of chromosome 1
  1. Chromosome 1 
    ... 1. 1p36 deletion syndrome is caused by a deletion of genetic material from a specific region in the short (p) arm of chromosome 1. The signs and symptoms of this disorder include ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  2. WAGR syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/wagr-syndrome - Genetics
  3. Cri-du-chat 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-. ...
    https://medlineplus.gov/genetics/condition/cri-du-chat-syndrome - Genetics
  4. Wolf-Hirschhorn syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/wolf-hirschhorn-syndrome - Genetics
  5. Smith-Magenis syndrome 
    ... 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. ...
    https://medlineplus.gov/genetics/condition/smith-magenis-syndrome - Genetics
  6. Chromosome 19 
    ... of genes varies. Chromosome 19 likely contains about 1,500 genes that provide instructions ... deletion of a small piece of the short (p) arm of chromosome 19 in each cell. Major features ...
    https://medlineplus.gov/genetics/chromosome/19 - Genetics
  7. Chromosome 20 
    ... in controlling the growth and division of cells. ... of the chromosome in each cell (partial trisomy 20p or 20q) or a missing segment ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics
  8. Chromosome 16 
    ... genes are missing as a result of this deletion in the short arm of chromosome 16. The deleted region includes the CREBBP gene, ... chromosome 16 include an extra segment of the short (p) or long (q) arm of the chromosome in each cell (partial trisomy 16p or 16q) and a missing segment ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  9. Chromosome 11 
    ... WAGR syndrome (described below) is caused by a deletion of genetic material from the short arm of chromosome 11 at a position designated 11p13. Occasionally, a ...
    https://medlineplus.gov/genetics/chromosome/11 - Genetics
  10. Chromosome 5 
    ... cat's cry) syndrome is caused by a deletion of the end of the short (p) arm of chromosome 5. This chromosomal change is written as 5p- ( ... severe intellectual disability and developmental delays than smaller ... short arm of chromosome 5 that are associated with particular features of ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
previous · 1 · 2 · 3 · next