An osteosclerotic form of Robinow syndrome-Reference-Cited by-同舟云学术

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An osteosclerotic form of Robinow syndrome

Published:2014-07-14 Issue:10 Volume:164 Page:2638-2642
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bunn Kieran J.¹,Lai Angeline²,Al-Ani Azza³,Farella Mauro³,Craw Susan⁴,Robertson Stephen P.¹

Affiliation:

1. Department of Women's and Children's Health; Dunedin School of Medicine; University of Otago; Dunedin New Zealand

2. Genetics Service; Department of Paediatrics; KK Women's and Children's Hospital; Singapore

3. Department of Oral Sciences; School of Dentistry; University of Otago; Dunedin New Zealand

4. Department of Radiology; Dunedin Hospital; Dunedin New Zealand

Funder

Curekids

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36677/fullpdf

Reference18 articles.

1. Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22;Afzal;Hum Genet,2000a

2. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2;Afzal;Nat Genet,2000b

3. Robinow syndrome without mesomelic ‘brachymelia’: A report of five cases;Bain;J Med Genet,1986

4. WNT signaling in bone homeostasis and disease: From human mutations to treatments;Baron;Nat Med,2013

5. Craniofacial and intraoral phenotype of Robinow syndrome forms;Beiraghi;Clin Genet,2011

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chondrocyte Polarity During Endochondral Ossification Requires Protein–Protein Interactions Between Prickle1 and Dishevelled2/3;Journal of Bone and Mineral Research;2021-09-28

2. Clinical and molecular characterization of four patients with Robinow syndrome from different families;American Journal of Medical Genetics Part A;2021-01-26

3. Craniofacial phenotypes associated with Robinow syndrome;American Journal of Medical Genetics Part A;2020-11-25

4. Extremity anomalies associated with Robinow syndrome;American Journal of Medical Genetics Part A;2020-09-25

5. Characterization of the Robinow syndrome skeletal phenotype, bone micro‐architecture, and genotype–phenotype correlations with the osteosclerotic form;American Journal of Medical Genetics Part A;2020-09-05

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