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

SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1).

Human molecular genetics - 1 May 1994

Lench N J, Brook A H, Winter G B

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 Amelogenesis Imperfecta
Share to Amelogenin
Share to Dental Enamel Proteins
Share to DNA Mutational Analysis

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

Share to DNA, Single-Stranded

Share to Nucleic Acid Conformation

Share to Sequence Deletion

Source

Identifiers

PMID: 8081371
DOI: 10.1093/hmg/3.5.827

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1).PMID 8081371Read ↗

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).Semantic proximity Read ↗

Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1).Semantic proximity Read ↗

DNA diagnosis of X-linked amelogenesis imperfecta (AIH1).Semantic proximity Read ↗

A novel AMELX mutation causes hypoplastic amelogenesis imperfecta.Semantic proximity Read ↗

Amplification failure of the amelogenin gene (AMELX) caused by a primer binding site mutation.Semantic proximity Read ↗

PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta.Semantic proximity Read ↗

An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the LiteratureSemantic proximity Read ↗

Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta.Semantic proximity Read ↗

Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4.Semantic proximity Read ↗

Detection of a Novel Mutation in X-linked Amelogenesis ImperfectaSemantic proximity Read ↗

Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.Semantic proximity Read ↗

Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome.Semantic proximity Read ↗

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