Development and progress of the National Congenital Anomaly and Rare Disease Registration Service

Sarah Stevens; Nicola Miller; Jeremy Rashbass

doi:10.1136/archdischild-2017-312833

Development and progress of the National Congenital Anomaly and Rare Disease Registration Service

Sarah Stevens^*, Nicola Miller, Jeremy Rashbass

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

Original language	English
Pages (from-to)	215-218
Number of pages	4
Journal	Archives of Disease in Childhood
Volume	103
Issue number	3
DOIs	https://doi.org/10.1136/archdischild-2017-312833
Publication status	Published - Mar 2018

Keywords

congenital abnorm
data collection
disease registration
public health
rare disease

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1136/archdischild-2017-312833

Cite this

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title = "Development and progress of the National Congenital Anomaly and Rare Disease Registration Service",

keywords = "congenital abnorm, data collection, disease registration, public health, rare disease",

author = "Sarah Stevens and Nicola Miller and Jeremy Rashbass",

year = "2018",

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language = "English",

volume = "103",

pages = "215--218",

journal = "Archives of Disease in Childhood",

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T1 - Development and progress of the National Congenital Anomaly and Rare Disease Registration Service

AU - Stevens, Sarah

AU - Miller, Nicola

AU - Rashbass, Jeremy

PY - 2018/3

Y1 - 2018/3

KW - congenital abnorm

KW - data collection

KW - disease registration

KW - public health

KW - rare disease

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DO - 10.1136/archdischild-2017-312833

M3 - Article

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AN - SCOPUS:85042920854

SN - 0003-9888

VL - 103

SP - 215

EP - 218

JO - Archives of Disease in Childhood

JF - Archives of Disease in Childhood

IS - 3

ER -

Development and progress of the National Congenital Anomaly and Rare Disease Registration Service

Keywords

UN SDGs

Access to Document

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