Works matching IS 09143505 AND DT 2013 AND VI 53 AND IP 4

Results: 10

Effects of maternal exposure to thiamazole on behavioral development in infant cynomolgus monkeys.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 149, doi. 10.1111/cga.12024
By:
- Inoue, Ayumi;
- Arima, Akihiro;
- Kato, Hirohito;
- Yamashita, Nobuyoshi;
- Nishida, Yoshiro;
- Ooshima, Yojiro;
- Ebihara, Shizufumi
Publication type:
Article
Prenatal diagnosis of cervical spinal cord compression in chondrodysplasia punctata brachytelephalangic type: A case report and literature review.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 160, doi. 10.1111/cga.12003
By:
- Ochiai, Daigo;
- Takamura, Kyoko;
- Nishimura, Gen;
- Ikeda, Toshiyuki;
- Yakubo, Kazumi;
- Fukuiya, Tatsuro
Publication type:
Article
Announcement.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. J5, doi. 10.1111/cga.12035
Publication type:
Article
Spatiotemporal patterns of the Huntingtin-interacting protein 1-related gene in the mouse head.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 141, doi. 10.1111/cga.12023
By:
- Masuda, Tomoyuki;
- Sakuma, Chie;
- Ueno, Takayuki;
- Yamada, Yuriko;
- Ohmomo, Hideki;
- Ueda, Shuichi;
- Yamagishi, Toshiyuki;
- Yaginuma, Hiroyuki
Publication type:
Article
Reviewers.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 176, doi. 10.1111/cga.12034
Publication type:
Article
Abnormal continuation of umbilical vein into extra-hepatic portal vein: Report of three cases.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 170, doi. 10.1111/cga.12020
By:
- Jaiman, Sunil;
- Nalluri, Hima Bindu
Publication type:
Article
Novel nucleotide mutation leading to a recurrent amino acid alteration in SH3BP2 in a patient with cherubism.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 166, doi. 10.1111/cga.12013
By:
- Sangu, Noriko;
- Shimosato, Tsuyoshi;
- Inoda, Hirosato;
- Shimada, Shino;
- Shimojima, Keiko;
- Ando, Tomohiro;
- Yamamoto, Toshiyuki
Publication type:
Article
Abstracts.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. A1, doi. 10.1111/cga.12033
Publication type:
Article
Challenges in genetic counseling because of intra-familial phenotypic variation of oral-facial-digital syndrome type 1.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 155, doi. 10.1111/j.1741-4520.2012.00384.x
By:
- Shimojima, Keiko;
- Shimada, Shino;
- Sugawara, Midori;
- Yoshikawa, Naomi;
- Niijima, Shinichi;
- Urao, Masahiko;
- Yamamoto, Toshiyuki
Publication type:
Article
Prenatal diagnosis and clinicopathologic examination of a case with diastematomyelia.
Published in:
Congenital Anomalies, 2013, v. 53, n. 4, p. 163, doi. 10.1111/cga.12008
By:
- Turgal, Mert;
- Ozyuncu, Ozgur;
- Talim, Beril;
- Yazicioglu, Aslihan;
- Onderoglu, Lutfu
Publication type:
Article