Works matching IS 24721727 AND DT 2018 AND VI 110 AND IP 7

Results: 9

Issue Information.

Published in:: Birth Defects Research, 2018, v. 110, n. 7, p. 547, doi. 10.1002/bdr2.1232
Publication type:: Article

Exome sequencing in syndromic brain malformations identifies novel mutations in <italic>ACTB</italic>, and <italic>SLC9A6</italic>, and suggests <italic>BAZ1A</italic> as a new candidate gene.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 587, doi. 10.1002/bdr2.1200

By:

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

Publication type:

Article

Improved safety margin for embryotoxicity in rats for the new endoperoxide artefenomel (OZ439) as compared to artesunate.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 553, doi. 10.1002/bdr2.1170

By:

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

Publication type:

Article

Cover Image.

Published in:: Birth Defects Research, 2018, v. 110, n. 7, p. 1, doi. 10.1002/bdr2.1231
Publication type:: Article

Metformin in the first trimester and risks for specific birth defects in the National Birth Defects Prevention Study.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 579, doi. 10.1002/bdr2.1199

By:

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

Publication type:

Article

Maternal occupational cadmium exposure and nonsyndromic orofacial clefts.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 603, doi. 10.1002/bdr2.1202

By:

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

Publication type:

Article

Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 610, doi. 10.1002/bdr2.1223

By:

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

Publication type:

Article

A neuropathological study of novel <italic>RTTN</italic> gene mutations causing a familial microcephaly with simplified gyral pattern.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 598, doi. 10.1002/bdr2.1204

By:

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

Publication type:

Article

Comparative organ system development: An update.

Published in:

Birth Defects Research, 2018, v. 110, n. 7, p. 551, doi. 10.1002/bdr2.1091

By:

Ridings, Jim

Publication type:

Article