| P2093 | author name string | Brenda J Wilson | |
| | Pranesh Chakraborty | |
| | Beth K Potter | |
| | Tim Ramsay | |
| | Christina Honeywell | |
| | Jennifer Milburn | |
| | Kimberly Gall | |
| | Makda H Araia | |
| P2860 | cites work | Informing parents about newborn screening | Q57194106 |
| | Informing parents about expanded newborn screening: influences on provider involvement | Q57646040 |
| | Serving the family from birth to the medical home. Newborn screening: a blueprint for the future - a call for a national agenda on state newborn screening programs | Q74187288 |
| | Factors affecting mothers' knowledge of genetic screening | Q79943789 |
| | Incorporating newborn screening into prenatal care | Q80028062 |
| | Recommendations for effective newborn screening communication: results of focus groups with parents, providers, and experts | Q83876561 |
| | Expanded newborn screening for biochemical disorders: the effect of a false-positive result | Q83895393 |
| | Newborn screening: toward a uniform screening panel and system | Q28246824 |
| | Newborn screening: an appeal for improved parent education | Q34165932 |
| | Addressing the vaccine confidence gap. | Q34191703 |
| | Research ethics. Research practice and participant preferences: the growing gulf. | Q34603471 |
| | State laws regarding the retention and use of residual newborn screening blood samples | Q34725754 |
| | Newborn screening education on the internet: a content analysis of North American newborn screening program websites | Q35263937 |
| | Public attitudes regarding the use of residual newborn screening specimens for research | Q35715208 |
| | Talking with parents before newborn screening | Q36275992 |
| | Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study. | Q36288211 |
| | A review of the psychosocial effects of false-positive results on parents and current communication practices in newborn screening | Q36569422 |
| | Informed choice and public health screening for children: the case of blood spot screening | Q37331854 |
| | Citizens' values regarding research with stored samples from newborn screening in Canada | Q39663893 |
| | Information and informed consent for neonatal screening: opinions and preferences of parents | Q40180415 |
| | Completeness and complexity of information available to parents from newborn-screening programs | Q40425937 |
| | New mothers' awareness of newborn screening, and their attitudes to the retention and use of screening samples for research purposes | Q46526984 |
| | Committee Opinion No. 481: Newborn screening | Q56777779 |
| | Why do patients want information if not to take part in decision making? | Q56778545 |
| | Newborn blood collections. Science gold mine, ethical minefield | Q56782240 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 963-970 | |
| P577 | publication date | 2012-08-16 | |
| P1433 | published in | Genetics in Medicine | Q15765508 |
| P1476 | title | Factors associated with knowledge of and satisfaction with newborn screening education: a survey of mothers | |
| P478 | volume | 14 | |