<--- Back to Details
First PageDocument Content
Genetic genealogy / Newborn screening / Propionic acidemia / Methylmalonic acidemia / Isovaleric acidemia / Maple syrup urine disease / Glutaric aciduria type 1 / Biotinidase deficiency / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Health / Rare diseases / Medicine
Date: 2011-07-21 16:18:35
Genetic genealogy
Newborn screening
Propionic acidemia
Methylmalonic acidemia
Isovaleric acidemia
Maple syrup urine disease
Glutaric aciduria type 1
Biotinidase deficiency
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Health
Rare diseases
Medicine

Agency of Human Services  Division of Maternal and Child Health  Children with Special Health Needs  Vermont Newborn Screening Program REFUSAL TO CONSENT to REPEAT NEWBORN SCREENING 

Add to Reading List

Source URL: healthvermont.gov

Download Document from Source Website

File Size: 77,24 KB

Share Document on Facebook

Similar Documents

TRACK 1: BEGINNING DNA RESEARCH presented by Andy Hochreiter 1-1: DNA: WHERE DO I START? Definition • Genetic genealogy is the application of genetics to traditional genealogy. Genetic genealogy uses

DocID: 1uKp7 - View Document

Introduction to Genetic Genealogy Barbara Rae-Venter, J.D., Ph.D. www.GenealogyConsult.com "Put a scientist to work on your genealogy"

DocID: 1tTDP - View Document

Free Genetic Genealogy (DNA) Seminar with a Guest Speaker from Family Tree DNA sponsored by the (LSCAPG) and the

DocID: 1sKX5 - View Document

Survey: 2017 Call for Presentations CALL FOR PRESENTATIONS 2017 SCGS Jamboree, Genetic Genealogy Conference, Workshops and Jamboree Extension Series Webinars Speaker Portal Dear Colleague:

DocID: 1sK0L - View Document

Genetic Genealogy Journey Genetic Genealogy Standards Debbie Parker Wayne, CG, CGLSM Advanced genealogical researchers have long recognized the need for standards to allow us to judge our work and the work of others. So

DocID: 1sG11 - View Document