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

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families.

Developmental dynamics : an official publication of the American Association of Anatomists - 1 Sept 2021

Zu Bailing, Wang Zhigang, Xu Yunlan, You Guoling, Fu Qihua

Abstract excerpt

BACKGROUND: Polydactyly and syndactyly are the most common hereditary limb malformations. Molecular genetic testing is of great significance for hereditary limb malformations, which can establish prognosis and recurrence risk of surgical intervention. METHODS: The present study aimed to identify the genetic etiologies of a three-generation family with postaxial polydactyly and a four-generation family with...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Homeodomain Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to INDEL Mutation

Share to Mutation

Share to Pedigree

Share to Peptides

Share to Syndactyly

Share to Transcription Factors

Source

Identifiers

PMID: 33533119
DOI: 10.1002/dvdy.310

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families.PMID 33533119Read ↗

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family.Semantic proximity Read ↗

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.Semantic proximity Read ↗

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.Semantic proximity Read ↗

Novel mutations of the HOXD13 gene in hand and foot malformations.Semantic proximity Read ↗

Genetic overview of postaxial polydactyly: Updated classificationSemantic proximity Read ↗

Complex postaxial polydactyly types A and B with camptodactyly, hypoplastic third toe, zygodactyly and other digit anomalies caused by a novel GLI3 mutation.Semantic proximity Read ↗

Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactylySemantic proximity Read ↗

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.Semantic proximity Read ↗

Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing.Semantic proximity Read ↗

Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.Semantic proximity Read ↗

Polydactyly: Clinical and molecular manifestationsSemantic proximity Read ↗

Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.Semantic proximity Read ↗

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