Birth Defects Research, Volume 110, Issue 7, Pages 547-617

The Table of Contents for Volume 110, Issue 7 of the journal Birth Defects Research is now available.

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Table of Contents

Editorial

Comparative organ system development: An update (pages 551-552)

Jim Ridings

Original Research Articles

Improved safety margin for embryotoxicity in rats for the new endoperoxide artefenomel (OZ439) as compared to artesunate (pages 553-578)

Robert L. Clark, Tammye L. Edwards, Monica Longo, Joseph Kinney, Don K. Walker, Jon Rhodes, Sally A. Clode, Thomas Rückle, Timothy Wells, Nicole Andenmatten, and Anna Christine Huber

Metformin in the first trimester and risks for specific birth defects in the National Birth Defects Prevention Study (pages 579-586)

Stephanie Dukhovny, Carla M. Van Bennekom, David R. Gagnon, Sonia Hernandez Diaz, Samantha E. Parker, Marlene Anderka, Martha M. Werler, and Allen A. Mitchell

Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene (pages 587-597)

Valerie Weitensteiner, Rong Zhang, Julia Bungenberg, Matthias Marks, Jan Gehlen, Damian J. Ralser, Alina C. Hilger, Amit Sharma, Johannes Schumacher, Ulrich Gembruch, Waltraut M. Merz, Albert Becker, Janine Altmüller, Holger Thiele, Bernhard G. Herrmann, Benjamin Odermatt, Michael Ludwig, and Heiko Reutter

Case Report

A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern (pages 598-602)

Suzanne Chartier, Caroline Alby, Lucile Boutaud, Sophie Thomas, Nadia Elkhartoufi, Jelena Martinovic, Josseline Kaplan, Alexandra Benachi, Didier Lacombe, Pascale Sonigo, Séverine Drunat, Michel Vekemans, Joël Agenor, Férechté Encha Razavi, and Tania Attie‐Bitach

Brief Reports

Maternal occupational cadmium exposure and nonsyndromic orofacial clefts (pages 603-609)

Jonathan Suhl, Paul A. Romitti, Yanyan Cao, Carissa M. Rocheleau, Trudy L. Burns, Kristin Conway, Preetha Rajaraman, AJ Agopian, Patricia Stewart, and the National Birth Defects Prevention Study

Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia (pages 610-617)

Nori Matsunami, Hari Shanmugam, Lisa Baird, Jeff Stevens, Janice L. Byrne, Douglas C. Barnhart, Carrie Rau, Marcia L. Feldkamp, Bradley A. Yoder, Mark F. Leppert, H. Joseph Yost, and Luca Brunelli

 

Teratology Society members who have a subscription to BDR may access the full articles via the Teratology website using your member login information. Members may access past issues of BDRA, BDRB, BDRC and Teratology via the Associated Titles links on the BDR website.

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