# Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/recessive-robinow-syndrome-allelic-to-dominant-brachydactyly-type-b-is-caused-by/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Ali R. Afzal,Anna Rajab,Christiane Fenske,Michael Oldridge,Navaratnam Elanko,E. Ternes-Pereira,Beyhan Tüysüz,Victoria A. Murday,Michael A. Patton,Andrew O.M. Wilkie,Steven Jeffery |
| Citations | 306 |
| DOI | 10.1038/78107 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W1485743594 |
| PMID | 10932186 |
| Type | article |
| Year | 2000 |

## Paper authors

- [Beyhan Tüysüz](https://scholariq.org/researchers/beyhan-tuysuz/)

## Paper primary topic

- [Wnt/β-catenin signaling in development and cancer](https://scholariq.org/topics/wnt-catenin-signaling-in-development-and-cancer/)

## Paper topics

- [Wnt/β-catenin signaling in development and cancer](https://scholariq.org/topics/wnt-catenin-signaling-in-development-and-cancer/)
- [Kruppel-like factors research](https://scholariq.org/topics/kruppel-like-factors-research/)
- [Developmental Biology and Gene Regulation](https://scholariq.org/topics/developmental-biology-and-gene-regulation/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.