Isolated hypoplasia of abdominal wall muscles associated with fetal ascites
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - January 1, 2016 Category: Genetics & Stem Cells Authors: Laura Travan, Samuele Naviglio, Gabriele Cont, Pierpaolo Brovedani, Riccardo Davanzo, Sergio Demarini Tags: Case Report Source Type: research
Homeobox family Hoxc localization during murine palate formation
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - December 31, 2015 Category: Genetics & Stem Cells Authors: Azumi Hirata, Kentaro Katayama, Takehito Tsuji, Hideto Imura, Nagato Natsume, Toshio Sugahara, Tetsuo Kunieda, Hiroaki Nakamura, Yoshinori Otsuki Tags: Original Article Source Type: research
A 5‐HT2A/2C receptor agonist, 1‐(2,5‐dimethoxy‐4‐iodophenyl)‐2‐aminopropane, mitigates developmental neurotoxicity of ethanol to serotonergic neurons
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - December 30, 2015 Category: Genetics & Stem Cells Authors: Tsukasa Ishiguro, Hiromi Sakata‐Haga, Yoshihiro Fukui Tags: Original Article Source Type: research
Interkinetic nuclear migration in the mouse embryonic ureteric epithelium: possible implication for congenital anomalies of the kidney and urinary tract (CAKUT)
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - December 29, 2015 Category: Genetics & Stem Cells Authors: Tomoyuki Motoya, Noriko Ogawa, Tetsuya Nitta, Ashiq Mahmood Rafiq, Esrat Jahan, Motohide Furuya, Akihiro Matsumoto, Jun Udagawa, Hiroki Otani Tags: Original Article Source Type: research
Expanding the mutation and clinical spectrum of Roberts syndrome
In conclusion, we report a novel ESCO2 mutation and expand the clinical spectrum of Roberts syndrome. This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - December 29, 2015 Category: Genetics & Stem Cells Authors: Hanan H. Afifi, Ghada M.H. Abdel‐Salam, Maha M. Eid, Angie M.S. Tosson, Wafaa Gh. Shousha, Amira A. Abdel Azeem, Mona K. Farag, Mennat I. Mehrez, Khaled R. Gaber Tags: Original Article Source Type: research
