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Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Survival of children with rare structural congenital anomalies: a multi-registry cohort study

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_dd08c0e1b5574f08bdb9c7543519f4b7

Survival of children with rare structural congenital anomalies: a multi-registry cohort study

About this item

Full title

Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Publisher

England: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2022-03, Vol.17 (1), p.142-142, Article 142

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Congenital anomalies are the leading cause of perinatal, neonatal and infant mortality in developed countries. Large long-term follow-up studies investigating survival beyond the first year of life in children with rare congenital anomalies are costly and sufficiently large standardized cohorts are difficult to obtain due to the rarity of some anom...

Alternative Titles

Full title

Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_dd08c0e1b5574f08bdb9c7543519f4b7

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_dd08c0e1b5574f08bdb9c7543519f4b7

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/s13023-022-02292-y

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