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

Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX)

Pediatric radiology - 1 May 1999

Savarirayan R

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 Anticoagulants
Share to Arylsulfatases
Share to Chondrodysplasia Punctata
Share to Fetal Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gestational Age

Share to Maternal Exposure

Share to Warfarin

Share to X Chromosome

Source

Identifiers

PMID: 10382206
DOI: 10.1007/s002470050598

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX)PMID 10382206Read ↗

Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome)Semantic proximity Read ↗

A novel EBP c.224T>A mutation supports the existence of a male-specific disorder independent of CDPX2.Semantic proximity Read ↗

Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctataSemantic proximity Read ↗

A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies.Semantic proximity Read ↗

X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findings.Semantic proximity Read ↗

[Analysis of clinical manifestation and genetic mutation in a child with X-linked chondrodysplasia punctata 2].Semantic proximity Read ↗

ATR-X syndrome: genetics, clinical spectrum, and management.Semantic proximity Read ↗

Brachytelephalangic chondrodysplasia punctata: a case series to further delineate the phenotype.Semantic proximity Read ↗

Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency.Semantic proximity Read ↗

Clinical and genetic analysis of a Korean patient with X-linked chondrodysplasia punctata: identification of a novel splicing mutation in the ARSE gene.Semantic proximity Read ↗

Syndactyly: phenotypes, genetics and current classification.Semantic proximity Read ↗

Major review: Exfoliation syndrome; advances in disease genetics, molecular biology, and epidemiologySemantic proximity Read ↗

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