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In appreciation.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 375, doi. 10.1002/pd.2022
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- Article
Sequence of cardiovascular changes in IUGR in pregnancies with and without preeclampsia.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 377, doi. 10.1002/pd.1990
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- Publication type:
- Article
Prenatal testing for a novel EBP missense mutation causing X-linked dominant chondrodysplasia punctata.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 384, doi. 10.1002/pd.1980
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- Publication type:
- Article
Fetal genital anomalies: an aid to diagnosis.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 389, doi. 10.1002/pd.1979
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- Article
Inhibin A measurement using an automated assay platform.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 399, doi. 10.1002/pd.1983
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- Article
First trimester screening for Down syndrome in rhesus negative women.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 404, doi. 10.1002/pd.1970
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- Article
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 408, doi. 10.1002/pd.1960
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- Publication type:
- Article
Analysis of multiple loci can increase reliability of detection of fetal Y-chromosome DNA in maternal plasma.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 412, doi. 10.1002/pd.1986
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- Publication type:
- Article
Anxiety levels in women undergoing prenatal maternal serum screening for Down syndrome: the effect of a fast reporting system by mobile phone short-message service.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 417, doi. 10.1002/pd.1988
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- Publication type:
- Article
Maternal serum ADAM12s in the late first trimester of pregnancies with Trisomy 21.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 422, doi. 10.1002/pd.1994
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- Publication type:
- Article
Refined fluorescent STR quantification of cell-free fetal DNA during pregnancy in physiological and Down syndrome fetuses.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 425, doi. 10.1002/pd.1996
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- Publication type:
- Article
Blastocyst trophectoderm biopsy and preimplantation genetic diagnosis for familial monogenic disorders and chromosomal translocations.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 434, doi. 10.1002/pd.1924
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- Publication type:
- Article
Pregnancy outcome following prenatal diagnosis of sex chromosome abnormalities in Mainland China.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 443, doi. 10.1002/pd.1982
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- Publication type:
- Article
First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoele.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 445, doi. 10.1002/pd.1989
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- Publication type:
- Article
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 447, doi. 10.1002/pd.1991
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- Publication type:
- Article
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter)
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- 2008
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- Publication type:
- Journal Article
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1→pter) and partial trisomy 10q (10q25.1→qter).
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 450, doi. 10.1002/pd.1993
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- Publication type:
- Article
Prenatal diagnosis of Pallister-Killian syndrome in two fetuses with increased nuchal translucency.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 454, doi. 10.1002/pd.1974
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- Publication type:
- Article
A case of a bloodstained amniotic fluid sample from a pregnant woman with Down syndrome analyzed by QF-PCR after low-speed centrifugation.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 457, doi. 10.1002/pd.1992
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- Publication type:
- Article
Retrospective detection of transaldolase deficiency in amniotic fluid: implications for prenatal diagnosis.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 460, doi. 10.1002/pd.2002
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- Publication type:
- Article
Correlation between ultrasound and pathological examination in a prenatal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 463, doi. 10.1002/pd.2003
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- Publication type:
- Article
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion.
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- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 466, doi. 10.1002/pd.2005
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- Publication type:
- Article
Current awareness in prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 469, doi. 10.1002/pd.1857
- Publication type:
- Article