Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome-Reference-Cited by-同舟云学术

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Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome

Published:2020-09-21 Issue:12 Volume:185 Page:3576-3583
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Schwartz David D.¹^ORCID,Fein Rachel H.¹^ORCID,Carvalho Claudia M. B.²^ORCID,Sutton V. Reid²^ORCID,Mazzeu Juliana F.³^ORCID,Axelrad Marni E.¹^ORCID

Affiliation:

1. Section of Psychology, Department of Pediatrics Baylor College of Medicine Houston Texas USA

2. Department of Molecular and Human Genetics Baylor College of Medicine Houston Texas USA

3. Faculty of Medicine Universidade de Brasília Brasília Brazil

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61854

Reference35 articles.

1. Extremity anomalies associated with Robinow syndrome

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

3. Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

4. Robinow syndrome: report of two patients and review of literature;Butler M. G.;Clinical Genetics,2008

Cited by 6 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. Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndrome;Disease Models & Mechanisms;2024-06-01

2. Dishevelled localization and function are differentially regulated by structurally distinct sterols;2024-05-15

3. Mechanistic studies in Drosophila and chicken give new insights into functions of DVL1 in dominant Robinow syndrome;Disease Models & Mechanisms;2023-04-01

4. Nuclear Dishevelled: An enigmatic role in governing cell fate and Wnt signaling;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2022-10

5. Phenotypic and mutational spectrum of ROR2 ‐related Robinow syndrome;Human Mutation;2022-05-10

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