Fetal capillary haemangioblastoma: an exceptional tumour. A review of the literature.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 979, doi. 10.1002/pd.452
- By:
- Publication type:
- Article
Works matching IS 01973851 AND DT 2002 AND VI 22 AND IP 11
Results: 25
1
2
Type II single umbilical artery (persistent vitelline artery) in an otherwise normal fetus.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1040, doi. 10.1002/pd.463
- By:
- Publication type:
- Article
3
Pulmonary agenesis with ipsilateral microtia: a laterality association or expanded Goldenhar complex? Response to a letter.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1054, doi. 10.1002/pd.445
- By:
- Publication type:
- Article
4
Currarino triad: concurrent US and MRI diagnosis in the fetus and the mother.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1005, doi. 10.1002/pd.455
- By:
- Publication type:
- Article
5
Risk of amniocentesis in women screened positive for Down syndrome with second trimester maternal serum markers.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1036, doi. 10.1002/pd.449
- By:
- Publication type:
- Article
6
Estimation of risk in second trimester serum screening for Down syndrome among women who have already had first trimester screening.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1051, doi. 10.1002/pd.426
- By:
- Publication type:
- Article
7
Degree of fetal umbilical venous constriction at the abdominal wall in a low-risk population at 20-40 weeks of gestation.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1022, doi. 10.1002/pd.462
- By:
- Publication type:
- Article
8
Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 973, doi. 10.1002/pd.444
- By:
- Publication type:
- Article
9
Prenatal diagnosis of ductus venosus agenesis and its association with cytogenetic/congenital anomalies.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 995, doi. 10.1002/pd.456
- By:
- Publication type:
- Article
10
Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus. Monika Schlegel, Alessandra Baumer, Mariluce Riegel, Ute Wiedemann and Albert Schnizel. Prenatal Diagnosis 22(5): 418-421
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1056, doi. 10.1002/pd.495
- Publication type:
- Article
11
Down syndrome maternal serum marker screening after 18 weeks' gestation.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1001, doi. 10.1002/pd.451
- By:
- Publication type:
- Article
12
Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysis.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1028, doi. 10.1002/pd.466
- By:
- Publication type:
- Article
13
McKusik-Kaufman syndrome: prenatal diagnosis, genetics and follow up.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1048, doi. 10.1002/pd.448
- By:
- Publication type:
- Article
14
Fetal bradycardia in the first trimester: an unusual presentation of atrial extrasystoles.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 976, doi. 10.1002/pd.450
- By:
- Publication type:
- Article
15
Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 957, doi. 10.1002/pd.403
- By:
- Publication type:
- Article
16
Perinatal management and outcome of prenatally diagnosed congenital diaphragmatic hernia: a 1995-2000 series in Rennes University Hospital.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 988, doi. 10.1002/pd.454
- By:
- Publication type:
- Article
17
Prenatal diagnosis of Pelizaeus-Merzbacher disease.
- Published in:
- 2002
- By:
- Publication type:
- Other
18
The early development of the fetal kidney-an in utero sonographic evaluation between 13 and 22 weeks' gestation.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 962, doi. 10.1002/pd.436
- By:
- Publication type:
- Article
19
Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1011, doi. 10.1002/pd.458
- By:
- Publication type:
- Article
20
Current Awareness in prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1057, doi. 10.1002/pd.274
- Publication type:
- Article
21
The influence of prenatal screening and termination of pregnancy on perinatal mortality rates.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 966, doi. 10.1002/pd.442
- By:
- Publication type:
- Article
22
Rapid diagnosis of triploidy of maternal origin using fluorescent PCR and DNA fragment analysis in the third trimester of pregnancy.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 984, doi. 10.1002/pd.453
- By:
- Publication type:
- Article
23
Evaluating the risk of tuberous sclerosis in cases with prenatal diagnosis of cardiac rhabdomyoma.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1044, doi. 10.1002/pd.464
- By:
- Publication type:
- Article
24
Right pulmonary agenesis with ipsilateral microtia: a new laterality association or part of the oculoauriculovertebral spectrum?
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1053, doi. 10.1002/pd.446
- By:
- Publication type:
- Article
25
Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 11, p. 1016, doi. 10.1002/pd.457
- By:
- Publication type:
- Article