NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypes-Reference-Cited by-同舟云学术

NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypes

Author:

McNiven Vanda¹,Ito Yoko A.²,Hartley Taila²,Kernohan Kristin²,Miller Elka³,Armour Christine M.²⁴,

Affiliation:

1. Division of Clinical and Metabolic Genetics; The Hospital for Sick Children; Toronto Ontario Canada

2. Children's Hospital of Eastern Ontario Research Institute; University of Ottawa; Ottawa Ontario Canada

3. Department of Medical Imaging; Children's Hospital of Eastern Ontario, University of Ottawa; Ottawa Ontario Canada

4. Regional Genetics Unit; Children's Hospital of Eastern Ontario; Ottawa Ontario Canada

Funder

Children's Hospital of Eastern Ontario Foundation

Genome Quebec

Ontario Research Fund

Ontario Genomics Institute

Canadian Institutes of Health Research

Genome Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference23 articles.

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1. Nidogen in development and disease;Frontiers in Cell and Developmental Biology;2024-03-14