A novel 2.4‐kb PHKA2 deletion in a boy with glycogen storage disease type IXa.
- Published in:
- Congenital Anomalies, 2024, v. 64, n. 2, p. 63, doi. 10.1111/cga.12555
- By:
- Publication type:
- Article
Works matching IS 09143505 AND DT 2024 AND VI 64 AND IP 2
Results: 6
1
2
Early prenatal diagnosis of spondylocostal dysostosis caused by a novel variant in MESP2.
- Published in:
- Congenital Anomalies, 2024, v. 64, n. 2, p. 61, doi. 10.1111/cga.12554
- By:
- Publication type:
- Article
3
Effect of valproic acid on the formation and migration of cranial neural crest cells at the early developmental stages in rat embryos.
- Published in:
- Congenital Anomalies, 2024, v. 64, n. 2, p. 47, doi. 10.1111/cga.12553
- By:
- Publication type:
- Article
4
Questionnaire survey on public awareness of cleft lip with/without palate in Mongolia.
- Published in:
- Congenital Anomalies, 2024, v. 64, n. 2, p. 40, doi. 10.1111/cga.12552
- By:
- Publication type:
- Article
5
Pyramidalis muscle formation during human embryonic and early fetal periods.
- Published in:
- Congenital Anomalies, 2024, v. 64, n. 2, p. 32, doi. 10.1111/cga.12551
- By:
- Publication type:
- Article
6
Issue Information.
- Published in:
- Congenital Anomalies, 2024, v. 64, n. 2, p. 29, doi. 10.1111/cga.12522
- Publication type:
- Article