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

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.

Journal of medical genetics - 1 May 2001

Vincent A, Billingsley G, Priston M, Williams-Lyn D, Sutherland J, Glaser T, Oliver E, Walter M A, Heathcote G, Levin A, Héon E

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 Aryl Hydrocarbon Hydroxylases
Share to Canada
Share to Cytochrome P-450 CYP1B1
Share to Cytochrome P-450 Enzyme System

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glaucoma

Share to Indians, North American

Share to Infant

Share to Infant, Newborn

Source

Open in PubMed Open full text

Identifiers

PMID: 11403040
DOI: 10.1136/jmg.38.5.324
PMCID: PMC1734880

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.PMID 11403040Read ↗

Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family.Semantic proximity Read ↗

Geographical Variability in CYP1B1 Mutations in Primary Congenital GlaucomaSemantic proximity Read ↗

Gene symbol: CYP1B1.Semantic proximity Read ↗

Gene symbol: CYP1B1.Semantic proximity Read ↗

Gene symbol: CYP1B1.Semantic proximity Read ↗

Gene symbol: CYP1B1.Semantic proximity Read ↗

Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients.Semantic proximity Read ↗

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.Semantic proximity Read ↗

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.Semantic proximity Read ↗

Clinical variability of mutations in the ABCB11 gene: a case report.Semantic proximity Read ↗

Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations.Semantic proximity Read ↗

Characterization of the biochemical and structural phenotypes of four CYP1B1 mutations observed in individuals with primary congenital glaucoma.Semantic proximity Read ↗

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