A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: Recommendations of the United States Secretary for Health and Human Services Advisory Committee on Heritable Disorders in Newborns and Children
- 1 February 2010
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 12 (2), 77-80
- https://doi.org/10.1097/gim.0b013e3181cb78fa
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Pharmacogenetics of Anti-Inflammatory Treatment in Children with Asthma: Rationale and Design of the PACMAN CohortPharmacogenomics, 2009
- Supporting Family Adaptation to Presymptomatic and "Untreatable" Conditions in an Era of Expanded Newborn ScreeningJournal of Pediatric Psychology, 2008
- Linking Family History in Obstetric and Pediatric Care: Assessing Risk for Genetic Disease and Birth DefectsPEDIATRICS, 2007
- Translational Research: Moving Discovery to PracticeClinical Pharmacology & Therapeutics, 2007
- Executive SummaryGenetics in Medicine, 2006
- ACOG Committee Opinion #325Obstetrics & Gynecology, 2005
- The Family History — More Important Than EverNew England Journal of Medicine, 2004
- Primary Care: Is There Enough Time for Prevention?American Journal of Public Health, 2003
- Personalized medicine: revolutionizing drug discovery and patient careTrends in Biotechnology, 2001
- Doppler Systolic-Diastolic Ratios in Pregnancies Complicated by SyphilisObstetrics & Gynecology, 1991