Found: 20
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Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 101, doi. 10.1002/pd.2172
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- Article
First-trimester nasal bone length in a normal Latin American population.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 108, doi. 10.1002/pd.2173
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- Article
A novel method for extracting DNA from chorionic villus samples for use in CVS-PCR, which ensures complete villus dissociation.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 113, doi. 10.1002/pd.2160
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- Article
Prenatal screening for Down syndrome: women's involvement in decision-making and their attitudes to screening.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 120, doi. 10.1002/pd.2183
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- Article
Second trimester prenatal ultrasound for the detection of pregnancies at increased risk of Trisomy 18 based on serum screening.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 129, doi. 10.1002/pd.2166
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- Article
Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 140, doi. 10.1002/pd.2167
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- Article
Assessing discrepant findings between QF-PCR on uncultured prenatal samples and karyotyping on long-term culture.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 151, doi. 10.1002/pd.2194
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- Article
Timing of referral for prenatal genetic counselling.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 156, doi. 10.1002/pd.2201
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- Article
Foetal craniopharyngioma diagnosed by prenatal ultrasonography and confirmed by histopathological examination.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 160, doi. 10.1002/pd.2202
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- Article
The attitude of women toward current and future possibilities of diagnostic testing in maternal blood using fetal DNA.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 164, doi. 10.1002/pd.2205
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- Article
Prenatal diagnosis of isolated fetal cerebellar hemorrhage associated with maternal septic shock.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 169, doi. 10.1002/pd.2155
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- Article
Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 172, doi. 10.1002/pd.2164
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- Article
Prenatal clinical characteristics of Casamassima-Morton-Nance syndrome.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 175, doi. 10.1002/pd.2168
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- Article
Positive maternal anti-SSA/SSB antibody-related fetal right ventricular endocardial fibroelastosis without atrioventricular block, reversal of endocardial fibroelastosis.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 177, doi. 10.1002/pd.2073
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- Article
Prenatal diagnosis of a complete sternal cleft in a child with PHACES syndrome-a case report.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 179, doi. 10.1002/pd.2117
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- Article
Prenatal diagnosis of Gollop-Wolfgang complex (tibial agenesis and femoral bifurcation).
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 182, doi. 10.1002/pd.2204
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- Article
Prenatal diagnosis of Nager syndrome in a monochorionic-diamniotic twin pregnancy.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 187, doi. 10.1002/pd.2214
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- Article
Down syndrome screening: determining the cutoff level of risk for invasive testing.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 190, doi. 10.1002/pd.2165
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Economic and policy decisions in prenatal screening.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 193, doi. 10.1002/pd.2189
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- Article
Current awareness in prenatal diagnosis.
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- Prenatal Diagnosis, 2009, v. 29, n. 2, p. 194, doi. 10.1002/pd.2095
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- Article