Issue Information.
- Published in:
- Congenital Anomalies, 2016, v. 56, n. 6, p. 245, doi. 10.1111/cga.12129
- Publication type:
- Article
Works matching IS 09143505 AND DT 2016 AND VI 56 AND IP 6
Results: 8
1
2
Prevalence of isomerism from a European registry: Live births, fetal deaths, and terminations of pregnancy.
- Published in:
- 2016
- By:
- Publication type:
- Other
3
Syndromic microphthalmia-3 caused by a mutation on gene SOX2 in a Colombian male patient.
- Published in:
- Congenital Anomalies, 2016, v. 56, n. 6, p. 250, doi. 10.1111/cga.12170
- By:
- Publication type:
- Article
4
A 16q12.2q21 deletion identified in a patient with developmental delay, epilepsy, short stature, and distinctive features.
- Published in:
- Congenital Anomalies, 2016, v. 56, n. 6, p. 253, doi. 10.1111/cga.12172
- By:
- Publication type:
- Article
5
Announcement.
- Published in:
- 2016
- Publication type:
- Other
6
Reviewers.
- Published in:
- 2016
- Publication type:
- Other
7
The 56th Annual Meeting of the Japanese Teratology Society: New Developments and Future Perspectives of Teratology Study - Translational Study to Link Teratology to Nutrition: Overview.
- Published in:
- Congenital Anomalies, 2016, v. 56, n. 6, p. 248, doi. 10.1111/cga.12191
- By:
- Publication type:
- Article
8
Abstracts.
- Published in:
- Congenital Anomalies, 2016, v. 56, n. 6, p. A1, doi. 10.1111/cga.12192
- Publication type:
- Article