MYT1 role in the microtia‐craniofacial microsomia spectrum-Reference-Cited by-同舟云学术

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MYT1 role in the microtia‐craniofacial microsomia spectrum

Published:2020-09 Issue:10 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Luquetti Daniela V.¹²^ORCID,Heike Carrie L.¹²,Zarante Ignacio³⁴,Timms Andrew E.²,Gustafson Jonas²,Pachajoa Harry⁵,Porras‐Hurtado Gloria L.⁶,Ayala‐Ramirez Paola³,Duenas‐Roque Milagros M.⁷,Jimenez Natalia⁸,Ibanez Lina M.⁸,Hurtado‐Villa Paula⁸

Affiliation:

1. University of Washington School of Medicine Seattle WA USA

2. Seattle Children's Research Institute Seattle WA USA

3. Human Genomics Institute Pontificia Universidad Javeriana Bogotá Colombia

4. Hospital Universitario San Ignacio Bogotá Colombia

5. Universidad Icesi Cali Colombia

6. Clinica Comfamiliar Risaralda Pereira Colombia

7. Hospital Edgardo Rebagliati Martins Lima Peru

8. Pontificia Universidad Javeriana Cali Colombia

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute of Dental and Craniofacial Research

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1401

Reference15 articles.

1. Oculo-auriculo-vertebral spectrum: a review of the literature and genetic update

2. A novel de novo mutation in MYT1, the unique OAVS gene identified so far

3. Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein treacle

4. Genome-wide occupancy links Hoxa2 to Wnt–β-catenin signaling in mouse embryonic development

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1. Application of genome and exome sequencing to study craniofacial conditions–A primer;Seminars in Orthodontics;2024-09

2. Syndrome de Goldenhar : étiologie, symptômes et croissance;Revue d'Orthopédie Dento-Faciale;2024-06

3. Bioinformatics Analysis of Hub Genes in Craniofacial Microsomia Combined With Congenital Heart Disease;Journal of Craniofacial Surgery;2024-05-09

4. Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997–2019;American Journal of Medical Genetics Part A;2024-03-30

5. Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum;2024-02-07

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