Found: 18
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Prenatal diagnosis of complete sole trisomy 1q.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 435, doi. 10.1002/pd.64
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- Article
Maternal serum levels of dimeric inhibin A in pregnancies affected by trisomy 21 in the first trimester.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 441, doi. 10.1002/pd.98
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- Article
Between pregnancy biological variability of first trimester markers of Down syndrome: implications for screening in subsequent pregnancies.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 445, doi. 10.1002/pd.94
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- Article
Attitude of Saudi families affected with hemoglobinopathies towards prenatal screening and abortion and the influence of religious ruling (Fatwa).
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 448, doi. 10.1002/pd.76
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- Article
Pulmonary stenosis and reactive right ventricular hypertrophy in the recipient fetus as a consequence of twin-to-twin transfusion.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 452, doi. 10.1002/pd.85
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- Article
Prenatal diagnosis of mosaicism for triploidy and trisomy 13.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 457, doi. 10.1002/pd.80
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- Article
Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for high rates of pregnancy termination.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 461, doi. 10.1002/pd.78
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- Publication type:
- Article
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephaly.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 466, doi. 10.1002/pd.92
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- Publication type:
- Article
Rapid and radical amniodrainage in the treatment of severe twin-twin transfusion syndrome<sup>†</sup>.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 471, doi. 10.1002/pd.96
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- Article
Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 477, doi. 10.1002/pd.95
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- Article
Complete karyotype discrepancy between placental and fetal cells in a case of ring chromosome 18.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 481, doi. 10.1002/pd.99
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- Article
Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 484, doi. 10.1002/pd.79
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- Publication type:
- Article
A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 490, doi. 10.1002/pd.109
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- Publication type:
- Article
Allele-specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 498, doi. 10.1002/pd.110
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- Article
Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 504, doi. 10.1002/pd.111
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- Article
Prenatal diagnosis of a fetus with megacystis and monosomy 21.
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- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 512, doi. 10.1002/pd.86
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- Article
Prenatal testing for uniparental disomy (UPD).
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 513, doi. 10.1002/pd.25
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- Article
Current Awareness.
- Published in:
- Prenatal Diagnosis, 2001, v. 21, n. 6, p. 515, doi. 10.1002/pd.11
- Publication type:
- Article