Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Caudal Regression Syndrome—A Review Focusing on Genetic Associations

19 Mar 2020

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital Anomalies and Fetal Surgery
Share to Congenital gastrointestinal and neural anomalies
Share to Urological Disorders and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32200015
DOI: 10.1016/j.wneu.2020.03.057

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Caudal Regression Syndrome—A Review Focusing on Genetic AssociationsPMID 32200015Read ↗

Caudal duplication syndrome: a literature review and reappraisal of its pathoembryogenesisSemantic proximity Read ↗

Sacral agenesis: A pilot whole exome sequencing and copy number studySemantic proximity Read ↗

Sacral agenesis: a pilot whole exome sequencing and copy number study.Semantic proximity Read ↗

Endocrine and behavioural features of Lowe syndrome and their potential molecular mechanisms.Semantic proximity Read ↗

Stepwise Developmental Regression Associated With Novel CACNA1A MutationSemantic proximity Read ↗

Selection Signatures Reveal Candidate Genes for the Cornish Rex Breed-Specific Phenotype.Semantic proximity Read ↗

Conceptual developments in the causes of Cockayne syndromeSemantic proximity Read ↗

Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.Semantic proximity Read ↗

HLXB9 homeobox gene and caudal regression syndrome.Semantic proximity Read ↗

Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome.Semantic proximity Read ↗

The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.Semantic proximity Read ↗

Genetic control of caudal development.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.