Found: 6
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Application of noninvasive prenatal testing in pregnancies with fetal double bubble sign: Is it feasible?
- Published in:
- 2018
- By:
- Publication type:
- journal article
A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α<sup>0</sup>-Thalassemia.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.
- Published in:
- Prenatal Diagnosis, 2020, v. 40, n. 11, p. 1426, doi. 10.1002/pd.5789
- By:
- Publication type:
- Article
α‐Haemoglobin pool measurement: a useful biomarker for evaluation of β‐thalassaemia intermedia?
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
A de novo ankyrin mutation (ANK1 Q109X) causing severe hereditary spherocytosis from preterm neonatal period.
- Published in:
- 2017
- By:
- Publication type:
- case study
Early prenatal detection of short‐rib polydactyly syndrome in a monochorionic diamniotic twin pregnancy.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 181, doi. 10.1111/cga.12317
- By:
- Publication type:
- Article