Announcement.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 206, doi. 10.1111/cga.12260
- Publication type:
- Article
Works matching IS 09143505 AND DT 2017 AND VI 57 AND IP 6
Results: 10
1
2
Neurological manifestations of 2q31 microdeletion syndrome.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 197, doi. 10.1111/cga.12212
- By:
- Publication type:
- Article
3
Relationship between epigenetic regulation, dietary habits, and the developmental origins of health and disease theory.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 184, doi. 10.1111/cga.12213
- By:
- Publication type:
- Article
4
Patient with a novel purine-rich element binding protein A mutation.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 201, doi. 10.1111/cga.12214
- By:
- Publication type:
- Article
5
Issue Information.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 173, doi. 10.1111/cga.12186
- Publication type:
- Article
6
D40/KNL1/CASC5 and autosomal recessive primary microcephaly.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 191, doi. 10.1111/cga.12252
- By:
- Publication type:
- Article
7
Abstracts.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. A1, doi. 10.1111/cga.12253
- Publication type:
- Article
8
Reviewers.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 205, doi. 10.1111/cga.12254
- Publication type:
- Article
9
57th Annual Meeting of the Japanese Teratology Society: Seeking a contact between humans and experimental animals.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 176, doi. 10.1111/cga.12256
- By:
- Publication type:
- Article
10
Undernourishment in utero and hepatic steatosis in later life: A potential issue in Japanese people.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 6, p. 178, doi. 10.1111/cga.12200
- By:
- Publication type:
- Article