Gary Neil Cramer offers NewBornGene ID from Syncier BioTech

NewBornGene ID ™ - This is a non-invasive genetic mutation test that can identify if someone is a carrier of multiple prevalent hereditary diseases that can be passed down unknowingly to children.

Diseases like Cystic Fibrosis, Tay-Sachs, Sickle Cell,Bloom Syndrome and many more; the test is for couples who are considering their first child, before,conception, or additional children. Women are tested and ifpositive the male is then tested. The samples for both tests arecollected through a simplemouthwash rinse. The Carrier Screening test that identifiesthose individuals who are carriers of the mutated recessive genes (theyare asymptomatic) isindicated for ALL patients between 18 and 45 wanting to have children either now or in the future. The test screens for 4,500 recessive mutations to identify only the 62 diseases that affect the greatest population (i.e.Cystic Fibrosis, Sickle Cell Anemia, SMA, Tay-Sachs, etc).

For more information please call Gary Neil Cramer at 360-909-0723.