Rapid detection of fetal aneuploidy using proteomics approaches on amniotic fluid supernatant.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 559, doi. 10.1002/pd.1186
- By:
- Publication type:
- Article
Works matching IS 01973851 AND DT 2005 AND VI 25 AND IP 7
Results: 26
1
2
Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene.
- Published in:
- 2005
- By:
- Publication type:
- journal article
3
Triploidy and trisomies in the offspring of a mother with a balanced translocation.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 623, doi. 10.1002/pd.1226
- By:
- Publication type:
- Article
4
The timing of demise in fetuses with trisomy 21 and trisomy 18.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 608, doi. 10.1002/pd.1243
- By:
- Publication type:
- Article
5
Prenatal fetal sex diagnosis by detecting amelogenin gene in maternal plasma.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 577, doi. 10.1002/pd.1192
- By:
- Publication type:
- Article
6
Current awareness in prenatal diagnosis.
- Published in:
- 2005
- Publication type:
- Bibliography
7
Educating general practitioners about prenatal testing: approaches and challenges.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 592, doi. 10.1002/pd.1202
- By:
- Publication type:
- Article
8
The importance of investigating an apparently simple Yq deletion detected prenatally.
- Published in:
- 2005
- By:
- Publication type:
- Case Study
9
Fragmentation of cell-free fetal DNA in plasma and urine of pregnant women.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 604, doi. 10.1002/pd.1213
- By:
- Publication type:
- Article
10
Hydrops fetalis and neonatal death from human parvovirus B19: an unusual complication.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 543, doi. 10.1002/pd.1168
- By:
- Publication type:
- Article
11
A novel pericentric inversion of chromosome 14 involving the rRNA gene cluster.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 620, doi. 10.1002/pd.1200
- By:
- Publication type:
- Article
12
Prenatal diagnosis of Bruck syndrome.
- Published in:
- 2005
- By:
- Publication type:
- journal article
13
Cornelia de Lange Syndrome in association with a balanced reciprocal translocation involving chromosomes 3 and 5.
- Published in:
- 2005
- By:
- Publication type:
- journal article
14
Prenatally diagnosed Arthrogryposis multiplex congenita due to pathological changes in the fetal heart rate pattern.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 625, doi. 10.1002/pd.1208
- By:
- Publication type:
- Article
15
Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy.
- Published in:
- 2005
- By:
- Publication type:
- Case Study
16
Fetal hyperechogenic kidney with normal amniotic fluid volume: a diagnostic dilemma.
- Published in:
- 2005
- By:
- Publication type:
- journal article
17
Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites.
- Published in:
- 2005
- By:
- Publication type:
- journal article
18
Detection of chromosome aberrations during prenatal genetic testing for single gene disorders.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 622, doi. 10.1002/pd.1214
- By:
- Publication type:
- Article
19
Which gestational age estimate to use in AFP screening for spina bifida?
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 623, doi. 10.1002/pd.1225
- By:
- Publication type:
- Article
20
Cardiac time intervals of normal fetuses using noninvasive fetal electrocardiography.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 546, doi. 10.1002/pd.1184
- By:
- Publication type:
- Article
21
The utility of an erythroblast scoring system and gender-independent short tandem repeat (STR) analysis for the detection of aneuploid fetal cells in maternal blood.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 586, doi. 10.1002/pd.1199
- By:
- Publication type:
- Article
22
Prenatal diagnosis of cranial vault defects.
- Published in:
- 2005
- By:
- Publication type:
- Letter
23
Cavum veli interpositi: prenatal diagnosis and postnatal outcome.
- Published in:
- 2005
- By:
- Publication type:
- journal article
24
Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?
- Published in:
- 2005
- By:
- Publication type:
- journal article
25
Fetus with a de novo supernumerary marker chromosome 16 and a Dandy-Walker malformation detected on ultrasound.
- Published in:
- 2005
- By:
- Publication type:
- journal article
26
Omphalopagus conjoining and twin-twin transfusion syndrome.
- Published in:
- 2005
- By:
- Publication type:
- Case Study