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Congenital Anomalies, Ahead of Print. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 28, 2017 Category: Genetics & Stem Cells Source Type: research
Extracranial outflow of particles solved in cerebrospinal fluid: Fluorescein injection study
Congenital Anomalies, EarlyView. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 21, 2017 Category: Genetics & Stem Cells Source Type: research
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Congenital Anomalies, Ahead of Print. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 21, 2017 Category: Genetics & Stem Cells Source Type: research
Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis
Congenital Anomalies, EarlyView. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 16, 2017 Category: Genetics & Stem Cells Source Type: research
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Congenital Anomalies, Ahead of Print. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 16, 2017 Category: Genetics & Stem Cells Source Type: research
Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis
(Source: Congenital Anomalies)
Source: Congenital Anomalies - November 16, 2017 Category: Genetics & Stem Cells Authors: Yumi Enomoto, Yoshinori Tsurusaki, Noriaki Harada, Noriko Aida, Kenji Kurosawa Tags: Note Source Type: research
Abstracts
(Source: Congenital Anomalies)
Source: Congenital Anomalies - November 5, 2017 Category: Genetics & Stem Cells Tags: Abstracts Source Type: research
Announcement
(Source: Congenital Anomalies)
Source: Congenital Anomalies - November 5, 2017 Category: Genetics & Stem Cells Tags: Society News Source Type: research
Reviewers
(Source: Congenital Anomalies)
Source: Congenital Anomalies - November 5, 2017 Category: Genetics & Stem Cells Tags: Acknowledgement Source Type: research
57th Annual Meeting of the Japanese Teratology Society: Seeking a contact between humans and experimental animals
(Source: Congenital Anomalies)
Source: Congenital Anomalies - November 5, 2017 Category: Genetics & Stem Cells Authors: Hiroaki Aoyama Tags: Overview Source Type: research
Issue Information
The joint meeting of the 57th Annual Meeting of the Japanese Teratology Society (JTS) and the 6th Annual Meeting of the Japan Society for Developmental Origins of Health and Disease was held on August 26 to 28, 2017 in Tokyo, Japan. Further details can be seen in the Overview by Aoyama in this issue.
The joint meeting of the 57th Annual Meeting of the Japanese Teratology Society (JTS) and the 6th Annual Meeting of the Japan Society for Developmental Origins of Health and Disease was held on August 26 to 28, 2017 in Tokyo, Japan. Further details can be seen in the Overview by Aoyama in this issue. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 5, 2017 Category: Genetics & Stem Cells Tags: Issue Information Source Type: research
Outcomes of an international volunteer surgical project for patients with cleft lip and/or cleft palate: A mission in developing Laos
Congenital Anomalies, EarlyView. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 3, 2017 Category: Genetics & Stem Cells Source Type: research
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Congenital Anomalies, Ahead of Print. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 3, 2017 Category: Genetics & Stem Cells Source Type: research
Repairability of skeletal alterations induced by sodium valproate in rats
Abstract
The present study aimed at examining postnatal repairability of sodium valproate (VPA)‐induced skeletal alterations in rats. VPA (400 mg/kg) or the vehicle (distilled water) was orally administrated to pregnant Sprague‐Dawley rats from gestation day (GD) 9 to 11. Fetuses and pups were obtained on GD 21 and postnatal day (PND) 11, respectively, and their skeletons were stained with Alizarin red S and Alcian blue and examined. VPA‐induced costal and vertebral alterations in the fetuses included discontinued rib cartilage, fused rib, full or short supernumerary rib, bipart ossification of thoracic centrum, supe...
Source: Congenital Anomalies - November 1, 2017 Category: Genetics & Stem Cells Authors: Yuka Kirihata, Yoshiki Ban, Chiaki Nakamori, Hironori Takagi, Tomonori Hashimoto, Shunsuke Tsutsumi Tags: Short Communication Source Type: research
Novel Sequence Variants in the MKKS Gene Cause Bardet ‐Biedl Syndrome with Intra‐ and Inter‐Familial Variable Phenotypes
Abstract
Bardet‐Biedl Syndrome (BBS) is a multisystem disorder involving retina, kidney, limbs and nervous system. Additional features associated with BBS include dental anomalies, cardiovascular defects, hearing loss and speech impairment (Beales et al. 199; Ullah and Umair et al. 2017). Diagnosis of BBS is based on the presence of four out of six primary or three primary and two secondary phenotypes. (Source: Congenital Anomalies)
Source: Congenital Anomalies - November 1, 2017 Category: Genetics & Stem Cells Authors: Asmat Ullah, Maryam Khalid, Muhammad Umair, Sher Alam Khan, Muhammad Bilal, Saadullah Khan, Wasim Ahmad Tags: Note Source Type: research
