Mónica Alejandra Rosales‐Reynoso
Datos Biográficos
| ID | 8660906 |
|---|---|
| NOMBRE | Mónica Alejandra Rosales‐Reynoso |
| NOMBRES | Mónica Alejandra |
| APELLIDO | Rosales‐Reynoso |
| FIRMA | REYNOSO M A R |
| AFILIACIONES | Mexican Social Security Institute |
| ORCID | 0000-0003-0387-4996 |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 1 |
| TOTAL DE CITAS | 0 |
| OBRAS COMO AUTOR | 1 |
| OBRAS COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2008 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2008 |
| ÍNDICE H | 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…
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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 obra) · Allele frequency (1 obra) · Autism Spectrum Disorder Research (1 obra) · Biology (1 obra) · Demography (1 obra) · FMR1 (1 obra) · Gene (1 obra) · Genetics (1 obra) · Genetics and Neurodevelopmental Disorders (1 obra) · Genomic variations and chromosomal abnormalities (1 obra)