The deletion in this present family is smaller than a deletion previously described in a multigenerational family that lacks any clinical phenotype. This report shows that a 5p14 deletion does not ...

necker.fr Weill-Marchesani syndrome ... of chromosome 19p13.3-p13.2 in a large AD WMS family and show that, despite clinical homogeneity, AD and AR WMS are genetically heterogeneous entities. Because ...

Oct. 17, 2024 — Researchers have cracked the code of plant-to-fungi communication in a new study. Using baker's yeast, the researchers discovered that the plant hormone strigolactone (SL ...

Here, to our knowledge, we present the first known case of a patient with TAR syndrome who developed Philadelphia-chromosome positive (Ph+) AML, which accounts for only about 1% of newly diagnosed AML ...

We present a report of the parental ages (n = 865) and parental origin of meiotic nondisjunction (n = 236) that are likely to show a predisposition in the etiology of Down syndrome (DS).

Genetics is the branch of science concerned with genes, heredity, and variation in living organisms. It seeks to understand the process of trait inheritance from parents to offspring, including ...

Asperger's syndrome refers to a high-functioning form of autism. Although it was once classified as its own condition, Asperger’s is no longer an official diagnosis in the Diagnostic and ...

Editor’s note: looks like GM has changed its mind about removing the LT trim from the 2025 Chevy Colorado, with a new Colorado LT on the way. As highlighted in sixth episode of the Chevy Society ...

This gene encodes alpha tubulin and is highly similar to mouse and rat Tuba1 gene. Northern blotting studies have shown that the gene expression is predominantly found in morphologically ...

Tourette syndrome is a neurological (nervous system) tic disorder. It causes people to make sudden movements or sounds they can’t control. These are called tics. For example, someone with ...

Most children with Rett syndrome have a mutation on the X chromosome, usually in a gene called MECP2. MECP2 is present in more than 95% of Rett cases. It isn't clear what exactly this gene does or ...

However, most people with Dandy-Walker syndrome can lead happy, healthy lives with the help of educational, occupational, and physical therapies. Zamora EA, Ahmad T. Dandy Walker malformation.