Announcement.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 237, doi. 10.1111/cga.12448
- Publication type:
- Article
Works matching IS 09143505 AND DT 2021 AND VI 61 AND IP 6
Results: 9
1
2
Reviewers.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 236, doi. 10.1111/cga.12447
- Publication type:
- Article
3
A rare congenital esophageal anomaly mimicking an isolated esophageal atresia: Kluth Type IV<sub>1a</sub> membranous esophageal atresia.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 208, doi. 10.1111/cga.12441
- By:
- Publication type:
- Article
4
Posterior cloaca: A rare subtype of a complex anorectal malformation.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 234, doi. 10.1111/cga.12440
- By:
- Publication type:
- Article
5
Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 220, doi. 10.1111/cga.12439
- By:
- Publication type:
- Article
6
Stage‐dependent function of Wnt5a during male external genitalia development.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 212, doi. 10.1111/cga.12438
- By:
- Publication type:
- Article
7
A homozygous variant in ABCA3 is associated with severe respiratory distress and early neonatal death.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 231, doi. 10.1111/cga.12437
- By:
- Publication type:
- Article
8
Noonan syndrome‐like phenotype in a patient with heterozygous ERF truncating variant.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 226, doi. 10.1111/cga.12435
- By:
- Publication type:
- Article
9
Issue Information.
- Published in:
- Congenital Anomalies, 2021, v. 61, n. 6, p. 205, doi. 10.1111/cga.12380
- Publication type:
- Article