Pavel Romero‐Espinoza
Biographic Data
| ID | 8660907 |
|---|---|
| NAME | Pavel Romero‐Espinoza |
| GIVEN NAMES | Pavel |
| FAMILY NAME | Romero‐Espinoza |
| SIGNATURE | ESPINOZA P R |
| AFFILIATIONS | Mexican Social Security Institute |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2008 |
| LATEST PUBLICATION YEAR | 2008 |
| H-INDEX | 0 |
Genetic variation of the FMR1 gene among four Mexican populations
Fragile X syndrome is the most common cause of inherited mental retardation; it is caused by expansion of CGG repeats in the first exon of the FMR1 gene. The number of CGG repeats varies between 6 and 50 triplets in normal individuals; the most common alleles have 29 or 30 repeats. Allelic patterns in the global populations are similar; however; some reports show statistical differences among several populations. In Mexico, except by a single rep…
No prominent works on this page.
Genetic variation of the FMR1 gene among four Mexican populations
Fragile X syndrome is the most common cause of inherited mental retardation; it is caused by expansion of CGG repeats in the first exon of the FMR1 gene. The number of CGG repeats varies between 6 and 50 triplets in normal individuals; the most common alleles have 29 or 30 repeats. Allelic patterns in the global populations are similar; however; some reports show statistical differences among several populations. In Mexico, except by a single rep…
Allele (1 work) · Allele frequency (1 work) · Autism Spectrum Disorder Research (1 work) · Biology (1 work) · Demography (1 work) · FMR1 (1 work) · Gene (1 work) · Genetics (1 work) · Genetics and Neurodevelopmental Disorders (1 work) · Genomic variations and chromosomal abnormalities (1 work)