Effort required to contact primary care providers after newborn screening identifies sickle cell trait

Por Christopher, Stephanie A., Collins, Jenelle L., Farrell, Michael H.
Publicado em 2012

A Qualitative Secondary Evaluation of Statewide Follow-Up Interviews for Abnormal Newborn Screening Results for Cystic Fibrosis and Sickle Cell Hemoglobinopathy

Por La Pean, Alison, Collins, Jenelle L., Christopher, Stephanie A., Eskra, Kerry L., Roedl, Sara, Tluczek, Audrey, Farrell, Michael H.
Publicado em 2012

Factors that Influence Parents’ Experience with Results Disclosure after Newborn Screening Identifies Genetic Carrier Status for Cystic Fibrosis or Sickle Cell Hemoglobinopathy

Por Collins, Jenelle L., La Pean, Alison, O’Tool, Faith, Eskra, Kerry L., Roedl, Sara J., Tluczek, Audrey, Farrell, Michael H.
Publicado em 2012

Improving Communication between Doctors and Parents after Newborn Screening

Por Farrell, Michael H., Christopher, Stephanie A., Tluczek, Audrey, Kennedy-Parker, Karen, La Pean, Alison, Eskra, Kerry, Collins, Jenelle, Hoffman, Gary, Panepinto, Julie, Farrell, Philip M.
Publicado em 2011

A method to assess the organizing behaviors used in physicians’ counseling of standardized parents after newborn genetic screening

Por Christopher, Stephanie A., Ahmad, Nadia Y., Bradford, Lisa, Collins, Jenelle L., Eskra, Kerry, La Pean Kirschner, Alison, O’Tool, Faith O., Roedl, Sara J., Farrell, Michael H.
Publicado em 2012