Literature DB >> 12919145

ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome.

C Bacchelli, L C Wilson, J A Cook, R M Winter, F R Goodman.   

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Year:  2003        PMID： 12919145     DOI： 10.1034/j.1399-0004.2003.00139.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

Review 1.  Wnt signaling in cartilage development and diseases: lessons from animal studies.

Authors:  Yu Usami; Aruni T Gunawardena; Masahiro Iwamoto; Motomi Enomoto-Iwamoto
Journal:  Lab Invest       Date:  2015-12-07       Impact factor: 5.662

2.  A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.

Authors:  Jiaqi Shao; Yue Liu; Shuyang Zhao; Weisheng Sun; Jie Zhan; Lihua Cao
Journal:  BMC Pediatr       Date:  2022-09-05       Impact factor: 2.567

3.  Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population.

Authors:  Litao Qin; Guiyu Lou; Liangjie Guo; Yuwei Zhang; Hongdan Wang; Li Wang; Qiaofang Hou; Hongyan Liu; Xichuan Li; Shixiu Liao
Journal:  Sci Rep       Date:  2018-08-24       Impact factor: 4.379

4.  Interdigital Hyperplasia in Holstein Cattle Is Associated With a Missense Mutation in the Signal Peptide Region of the Tyrosine-Protein Kinase Transmembrane Receptor Gene.

Authors:  Xuying Zhang; Hermann H Swalve; René Pijl; Frank Rosner; Monika Wensch-Dorendorf; Bertram Brenig
Journal:  Front Genet       Date:  2019-11-13       Impact factor: 4.599
  4 in total

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