Researchers at Baylor College of Medicine, the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital, Baylor Genetics and collaborating institutions provided a ...

The average IQ is around 100 points. However, for people who may develop a psychotic illness, such as those with a microdeletion of chromosome 22, the average drops to 70-80 points.

Study: PARK2 Microdeletion or Duplications Have Been Implicated in Different Neurological Disorders Including Early Onset Parkinson Diseas e. Image Credit: MattLphotography / Shutterstock About ...

We're overjoyed to share that our sweet girl, Aurora, has tested negative for the rare condition known as microdeletion 1q21.1," Blanchard wrote in a statement on social media.

We're overjoyed to share that our sweet girl, Aurora, has tested negative for the rare condition known as microdeletion 1q21.1," Blanchard wrote in a statement on social media.

According to MedlinePlus, microdeletion 1Q21.1 is “a chromosomal change in which a small piece of chromosome 1 is deleted in each cell” and can lead to “delayed development” in children ...

Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. The American Journal of Human Genetics, 2018; 102 (2): 296 DOI: 10.1016/j.ajhg.2018.01.005 ...

When a microdeletion occurs in an individual’s DNA, the individual is considered to have a type of genetic disorder called a microdeletion syndrome. The different kinds of genomic disorders, including ...

Correspondence Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome Published November 10, 2011 N Engl J Med 2011;365: 1847 - 1848 DOI: 10.1056/NEJMc1106975 ...

Williams–Beuren syndrome, a multisystem disorder caused by the deletion of a chromosome region of 1.5 million to 1.8 million base pairs containing 26 to 28 genes, is a disorder of microdeletion ...

The 17q21.31 microdeletion syndrome is characterised by intellectual disability, epilepsy, distinctive facial dysmorphism, and congenital anomalies. To date, all individuals reported with this ...

Article Published: 27 May 2009 A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients Hartmut Engels, Eva Wohlleber, Alexander ...