Found: 9
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Announcement.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 78, doi. 10.1111/cga.12274
- Publication type:
- Article
Comment on “A prospective study on fetal posterior cranial fossa assessment for early detection of open spina bifida at 11–13 weeks” by Kose et al.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 77, doi. 10.1111/cga.12265
- By:
- Publication type:
- Article
Issue Information.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 45, doi. 10.1111/cga.12246
- Publication type:
- Article
Interkinetic nuclear migration in the tracheal and esophageal epithelia of the mouse embryo: Possible implications for tracheo‐esophageal anomalies.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 62, doi. 10.1111/cga.12241
- By:
- Publication type:
- Article
Pentalogy of Cantrell in a monozygotic twin with a giant omphalocele firmly attached to the amniotic membrane: Successful prenatal diagnosis and cesarean delivery.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 73, doi. 10.1111/cga.12237
- By:
- Publication type:
- Article
Unilateral lung agenesis, aplasia or hypoplasia: Which one is it?
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 75, doi. 10.1111/cga.12239
- By:
- Publication type:
- Article
Congenital duodenal and multiple jejunal atresia with malrotation in a patient with Down syndrome.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 71, doi. 10.1111/cga.12236
- By:
- Publication type:
- Article
Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 56, doi. 10.1111/cga.12235
- By:
- Publication type:
- Article
Three‐dimensional models of the segmented human fetal brain generated by magnetic resonance imaging.
- Published in:
- Congenital Anomalies, 2018, v. 58, n. 2, p. 48, doi. 10.1111/cga.12229
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- Publication type:
- Article