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

[Exclusion of candidate genes in a family with amelogenesis imperfecta].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology - 1 Jun 2007

Wang Xi-Jun, Ji Ping, Guo Hong-Mei, Yi Xin-Zhu

Abstract excerpt

OBJECTIVE: To localize the gene (s) responsible for autosomal dominant hypocalcified amelogenesis imperfecta in a Chinese family. METHODS: A Chinese family which was diagnosed as autosomal dominant hypocalcified amelogenesis imperfecta (AD) was studied. Venous blood from nineteen family members was collected and genomic DNA was extracted from the blood. Eight short tandem repeats (STRs) spanning five hereditary...

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 Dental Enamel Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Pedigree

Source

Identifiers

PMID: 17629198

Genes

AMBN
ENAM
KLK4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

[Exclusion of candidate genes in a family with amelogenesis imperfecta].PMID 17629198Read ↗

Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.Semantic proximity Read ↗

Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.Semantic proximity Read ↗

Molecular characterization of amelogenesis imperfecta in Chinese patients.Semantic proximity Read ↗

Candidate-gene exclusion in a family with inherited non-syndromic dental disorders.Semantic proximity Read ↗

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.Semantic proximity Read ↗

A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3.Semantic proximity Read ↗

Mutational analysis of candidate genes in 24 amelogenesis imperfecta families.Semantic proximity Read ↗

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.Semantic proximity Read ↗

[Genetic, clinical and molecular analysis of a family affected by amelogenesis imperfecta].Semantic proximity Read ↗

Autosomal-dominant Hypoplastic Form of Amelogenesis Imperfecta Caused by an Enamelin Gene Mutation at the Exon-Intron BoundarySemantic proximity Read ↗

Target gene analyses of 39 amelogenesis imperfecta kindreds.Semantic proximity Read ↗

ENAM mutations with incomplete penetrance.Semantic proximity Read ↗

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