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)
- Published in:
- 2008
- By:
- Publication type:
- Journal Article
Works matching IS 01973851 AND DT 2008 AND VI 28 AND IP 5
Results: 23
1
2
Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 408, doi. 10.1002/pd.1960
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- Publication type:
- Article
3
Pregnancy outcome following prenatal diagnosis of sex chromosome abnormalities in Mainland China.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 443, doi. 10.1002/pd.1982
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- Publication type:
- Article
4
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).
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 450, doi. 10.1002/pd.1993
- By:
- Publication type:
- Article
5
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
6
Analysis of multiple loci can increase reliability of detection of fetal Y-chromosome DNA in maternal plasma.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 412, doi. 10.1002/pd.1986
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- Publication type:
- Article
7
Correlation between ultrasound and pathological examination in a prenatal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 463, doi. 10.1002/pd.2003
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- Publication type:
- Article
8
Fetal genital anomalies: an aid to diagnosis.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 389, doi. 10.1002/pd.1979
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- Publication type:
- Article
9
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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- Publication type:
- Article
10
A case of a bloodstained amniotic fluid sample from a pregnant woman with Down syndrome analyzed by QF-PCR after low-speed centrifugation.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 457, doi. 10.1002/pd.1992
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- Publication type:
- Article
11
Prenatal diagnosis of Pallister-Killian syndrome in two fetuses with increased nuchal translucency.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 454, doi. 10.1002/pd.1974
- By:
- Publication type:
- Article
12
Refined fluorescent STR quantification of cell-free fetal DNA during pregnancy in physiological and Down syndrome fetuses.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 425, doi. 10.1002/pd.1996
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- Publication type:
- Article
13
Retrospective detection of transaldolase deficiency in amniotic fluid: implications for prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 460, doi. 10.1002/pd.2002
- By:
- Publication type:
- Article
14
First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoele.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 445, doi. 10.1002/pd.1989
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- Publication type:
- Article
15
Current awareness in prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 469, doi. 10.1002/pd.1857
- Publication type:
- Article
16
Prenatal testing for a novel EBP missense mutation causing X-linked dominant chondrodysplasia punctata.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 384, doi. 10.1002/pd.1980
- By:
- Publication type:
- Article
17
Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 447, doi. 10.1002/pd.1991
- By:
- Publication type:
- Article
18
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.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 417, doi. 10.1002/pd.1988
- By:
- Publication type:
- Article
19
Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 466, doi. 10.1002/pd.2005
- By:
- Publication type:
- Article
20
Sequence of cardiovascular changes in IUGR in pregnancies with and without preeclampsia.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 377, doi. 10.1002/pd.1990
- By:
- Publication type:
- Article
21
Inhibin A measurement using an automated assay platform.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 399, doi. 10.1002/pd.1983
- By:
- Publication type:
- Article
22
Maternal serum ADAM12s in the late first trimester of pregnancies with Trisomy 21.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 422, doi. 10.1002/pd.1994
- By:
- Publication type:
- Article
23
In appreciation.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 5, p. 375, doi. 10.1002/pd.2022
- By:
- Publication type:
- Article