PBX‐WNT‐P63‐IRF6 pathway in nonsyndromic cleft lip and palate-Reference-Cited by-同舟云学术

PBX‐WNT‐P63‐IRF6 pathway in nonsyndromic cleft lip and palate

Published:2019-12-11 Issue:3 Volume:112 Page:234-244
ISSN:2472-1727
Container-title:Birth Defects Research
language:en
Short-container-title:Birth Defects Research

Author:

Maili Lorena¹^ORCID,Letra Ariadne²³^ORCID,Silva Renato³⁴,Buchanan Edward P.⁵,Mulliken John B.⁶,Greives Matthew R.⁷,Teichgraeber John F.⁷,Blackwell Steven J.⁸,Ummer Rohit³,Weber Ryan³,Chiquet Brett³⁹,Blanton Susan H.¹⁰,Hecht Jacqueline T.¹³

Affiliation:

1. Department of PediatricsUniversity of Texas Health Science Center McGovern Medical School at Houston Houston Texas

2. Department of Diagnostic and Biomedical SciencesUniversity of Texas Health Science Center School of Dentistry at Houston Houston Texas

3. Center for Craniofacial ResearchUniversity of Texas Health Science Center School of Dentistry at Houston Houston Texas

4. Department of EndodonticsUniversity of Texas Health Science Center School of Dentistry at Houston Houston Texas

5. Department of Plastic SurgeryTexas Children's Hospital Houston Texas

6. Boston Children's Hospital Boston Massachusetts

7. Department of Pediatric SurgeryUniversity of Texas Health Science Center McGovern Medical School at Houston Houston Texas

8. Shriners Hospital for Children Houston Houston Texas

9. Department of Pediatric DentistryUniversity of Texas Health Science Center School of Dentistry at Houston Houston Texas

10. Dr. John T. MacDonald Foundation Department of Human GeneticsJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine Miami Florida

Funder

National Institutes of Health

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bdr2.1630

Reference76 articles.

1. Fine Tuning of Craniofacial Morphology by Distant-Acting Enhancers

2. Haploview: analysis and visualization of LD and haplotype maps

3. Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts