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Article

Brachydactyly type B1: report of a family with de novo ROR2 mutation.

Clinical genetics - 1 Dec 2006

Hamamy H, Saleh N, Oldridge M, Al-Hadidy A, Ajlouni K

Abstract excerpt

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Topics

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Share to Foot Deformities, Congenital
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Receptor Tyrosine Kinase-like Orphan Receptors

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Source

Identifiers

PMID: 17101003
DOI: 10.1111/j.1399-0004.2006.00719.x

Genes

ROR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Brachydactyly type B1: report of a family with de novo ROR2 mutation.PMID 17101003Read ↗

A new mutation in the gene ROR2 causes brachydactyly type B1.Semantic proximity Read ↗

[Genetic analysis of a Chinese pedigree affected with Brachydactyly type B1 due to a novel variant of ROR2 gene].Semantic proximity Read ↗

A nonsense mutation in the gene ROR2 underlying autosomal dominant brachydactyly type B.Semantic proximity Read ↗

Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.Semantic proximity Read ↗

[Identification of a recurrent mutation in the ROR2 gene in a Chinese family with brachydactyly type B].Semantic proximity Read ↗

One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.Semantic proximity Read ↗

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.Semantic proximity Read ↗

BMPR1B gene in brachydactyly type 2-A family with de novo R486W mutation and a disease phenotype.Semantic proximity Read ↗

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.Semantic proximity Read ↗

ROR-Family Receptor Tyrosine Kinases.Semantic proximity Read ↗

Brachydactyly A1: new relatives for old families?Semantic proximity Read ↗

Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.Semantic proximity Read ↗

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