Found: 24
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Prediction of the rate of decline in fetal hemoglobin levels between first and second transfusions in red cell alloimmune disease.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1123, doi. 10.1002/pd.3966
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- Publication type:
- Article
Percutaneous laser ablation under ultrasound guidance for fetal hyperechogenic microcystic lung lesions with hydrops: a single center cohort and a literature review.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1127, doi. 10.1002/pd.3969
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- Publication type:
- Article
Prenatal genetic counseling and consanguinity.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1133, doi. 10.1002/pd.3971
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- Publication type:
- Article
Fast protocol for the diagnosis of lysosomal diseases in nonimmune hydrops fetalis.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1139, doi. 10.1002/pd.3972
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- Publication type:
- Article
Assessment of the posterior brain at 11-14 weeks for the prediction of open neural tube defects.
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- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1143, doi. 10.1002/pd.3973
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- Publication type:
- Article
Optimal cut-offs for Down syndrome contingent screening in a population of 10,156 pregnant women.
- Published in:
- 2012
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- Publication type:
- journal article
Optimal cut-offs for down syndrome contingent screening in a population of 10 156 pregnant women.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1147, doi. 10.1002/pd.3974
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- Publication type:
- Article
Experts' opinions on the benefit of an incidental prenatal diagnosis of sex chromosomal aneuploidy: a qualitative interview survey.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1151, doi. 10.1002/pd.3975
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- Publication type:
- Article
Reproducibility study of crown-rump length and biparietal diameter measurements in the first trimester.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1158, doi. 10.1002/pd.3976
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- Publication type:
- Article
Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1166, doi. 10.1002/pd.3977
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- Publication type:
- Article
Early second trimester maternal plasma levels of thrombin-inhibitor complexes and subsequent spontaneous preterm delivery.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1170, doi. 10.1002/pd.3978
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- Publication type:
- Article
Two-dimensional and three-dimensional Doppler assessment of fetal growth restriction with different severity and onset.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1174, doi. 10.1002/pd.3980
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- Publication type:
- Article
Arabin cervical pessary to prevent preterm birth in severe twin-to-twin transfusion syndrome treated by laser surgery.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1181, doi. 10.1002/pd.3982
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- Publication type:
- Article
Evaluation of normal fetal pulmonary veins using B-flow imaging with spatiotemporal image correlation and by traditional color Doppler echocardiography.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1186, doi. 10.1002/pd.3983
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- Publication type:
- Article
Maternal serum second trimester screening for chromosomal disorders and neural tube defects in a government hospital of North India.
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- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1192, doi. 10.1002/pd.3984
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- Publication type:
- Article
Quantitative fluorescence PCR analysis of >40 000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X.
- Published in:
- 2012
- By:
- Publication type:
- Journal Article
Quantitative fluorescence PCR analysis of >40 000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X Quantitative fluorescence PCR analysis of >40 000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1197, doi. 10.1002/pd.3986
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- Publication type:
- Article
The discourse around usefulness, morality, risk and trust: a focus group study on prenatal genetic testing.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1205, doi. 10.1002/pd.3990
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- Publication type:
- Article
Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1212, doi. 10.1002/pd.3981
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- Publication type:
- Article
Islam and termination of pregnancy for genetic conditions in Pakistan: implications for Pakistani health care providers.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1218, doi. 10.1002/pd.3987
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- Publication type:
- Article
Comment on 'Origin of trisomy: no evidence to support the ovarian mosaicism theory'.
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- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1221, doi. 10.1002/pd.3958
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- Publication type:
- Article
Comment on "Relationship of first-trimester uterine artery Doppler to late stillbirth".
- Published in:
- 2012
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- Publication type:
- letter
Comment on 'Relationship of first-trimester uterine artery Doppler to late stillbirth'.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1222, doi. 10.1002/pd.3963
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- Publication type:
- Article
Authors' reply regarding 'Relationship of first-trimester uterine artery Doppler to late stillbirth'.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1223, doi. 10.1002/pd.3970
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- Publication type:
- Article