Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 1, p. 4, doi. 10.1111/cga.12173
- By:
- Publication type:
- Article
Works matching IS 09143505 AND DT 2017 AND VI 57 AND IP 1
Results: 9
1
2
Impact of the introduction of Non-invasive prenatal genetic testing on invasive tests: A single-center study in Japan.
- Published in:
- 2017
- By:
- Publication type:
- Other
3
Cartilage-hair hypoplasia associated with isolated hypoganglionosis: A case report.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 1, p. 32, doi. 10.1111/cga.12175
- By:
- Publication type:
- Article
4
Prenatal diagnosis of Fraser syndrome using routine ultrasound examination, confirmed by exome sequencing: Report of a novel homozygous missense FRAS1 mutation.
- Published in:
- 2017
- By:
- Publication type:
- Other
5
Dynamics of gyrification in the human cerebral cortex during development.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 1, p. 8, doi. 10.1111/cga.12179
- By:
- Publication type:
- Article
6
Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 1, p. 15, doi. 10.1111/cga.12180
- By:
- Publication type:
- Article
7
Issue Information.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 1, p. 1, doi. 10.1111/cga.12181
- Publication type:
- Article
8
Foxc2<sup> CreERT2</sup> knock-in mice mark stage-specific Foxc2-expressing cells during mouse organogenesis.
- Published in:
- Congenital Anomalies, 2017, v. 57, n. 1, p. 24, doi. 10.1111/cga.12198
- By:
- Publication type:
- Article
9
Announcement.
- Published in:
- 2017
- Publication type:
- Other