The Table of Contents for Volume 112, Issue 19 of the journal Birth Defects Research Special Issue: Orofacial Clefts is now available. This special issue is edited by Drs. Michiko Watanabe and Chengji J. Zhou and is freely available HERE for two months. After that time, BDRP who have a subscription to BDR may access the full articles via the BDRP website using your member login information, by clicking HERE.
Individuals without a subscription may peruse the current and past issue tables of contents, abstracts, and any freely available papers and special issues, by visiting the journal on the Wiley website, by clicking HERE.
EDITORIAL
Introduction to the special issue on orofacial clefts
Michiko Watanabe, Chengji J. Zhou
First Published: 30 October 2020
REVIEW ARTICLES
Cellular and developmental basis of orofacial clefts
Yu Ji, Michael A. Garland, Bo Sun, Shuwen Zhang, Kurt Reynolds, Moira McMahon, Ratheya Rajakumar, Mohammad S. Islam, Yue Liu, YiPing Chen, Chengji J. Zhou
First Published: 29 July 2020
Genetics and signaling mechanisms of orofacial clefts
Kurt Reynolds, Shuwen Zhang, Bo Sun, Michael A. Garland, Yu Ji, Chengji J. Zhou
First Published: 15 July 2020
Role of epigenetics and miRNAs in orofacial clefts
Michael A. Garland, Bo Sun, Shuwen Zhang, Kurt Reynolds, Yu Ji, Chengji J. Zhou
First Published: 14 September 2020
Environmental mechanisms of orofacial clefts
Michael A. Garland, Kurt Reynolds, Chengji J. Zhou
First Published: 30 October 2020
Folate intake, markers of folate status and oral clefts: An updated set of systematic reviews and meta‐analyses
Yulai Zhou, Vigigah Sinnathamby, Yamei Yu, Lindsey Sikora, Candice Y. Johnson, Peter Mossey, Julian Little
First Published: 29 October 2020
CASE REPORTS
Neural crest derivatives and neuroendocrine cells in the gut of anencephalic and fetuses without congenital defects
Samuel Bencomo‐Loeppky, Jorge Arturo García‐Rizk, Hugo Alberto Cervantes‐Flores, Margarita Levario‐Carrillo, Ricardo Fierro Murga, Sandra Alicia Reza‐López, Martha Loya‐Loya, Dora Virginia Chávez‐Corral
First Published: 11 September 2020
Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes
Katherine Abell, Leandra Tolusso, Nicki Smith, Robert Hopkin, Marissa Vawter‐Lee, Mounira Habli, Stefanie Riddle, Maria A. Calvo‐Garcia, Qiaoning Guan, Karin Bierbrauer, Vivian Hwa, Howard M. Saal
First Published: 15 September 2020
Prenatal and foetal autopsy findings in glutaric aciduria type II
Adriano Martinez‐Aracil, Rebeca Ruiz‐Onandi, Alvaro Perez‐Rodriguez, Amaia Sagasta, Isabel Llano‐Rivas, Guiomar Perez de Nanclares
First Published: 22 September 2020
