Practice variation of genetic counselor engagement in the cystic fibrosis newborn screen-positive diagnostic resolution process.

Langfelder-Schwind, Elinor; Raraigh, Karen S; Parad, Richard B

Langfelder-Schwind, Elinor; Raraigh, Karen S; Parad, Richard B.

Affiliation

Langfelder-Schwind E; The Cystic Fibrosis Center, Mount Sinai Beth Israel, Department of Pulmonary, Critical Care, and Sleep Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Raraigh KS; Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Parad RB; Department of Pediatric Newborn Medicine, Brigham and Women's Hospital, Boston, MA, USA.

J Genet Couns ; 28(6): 1178-1188, 2019 12.

Article in En | MEDLINE | ID: mdl-31550062

Subject(s)

Counselors; Cystic Fibrosis/genetics; Genetic Counseling/methods; Neonatal Screening/methods; Cystic Fibrosis Transmembrane Conductance Regulator/genetics; Genetic Testing; Health Services Accessibility; Humans; Infant, Newborn; Quality of Life; Surveys and Questionnaires

Key words

CRMS/CFSPID; cystic fibrosis; genetic counseling; genetic counselors; multidisciplinary care; newborn screening; public health; service delivery models; workforce

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neonatal Screening / Cystic Fibrosis / Counselors / Genetic Counseling Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Newborn Language: En Journal: J Genet Couns Journal subject: GENETICA MEDICA Year: 2019 Type: Article Affiliation country: United States

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