Prenatal diagnosis of Apert syndrome: report of two cases.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1009, doi. 10.1002/pd.744
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- Publication type:
- Article
Works matching IS 01973851 AND DT 2003 AND VI 23 AND IP 12
Results: 16
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2
Prenatal diagnosis and genetic analysis of WiskottAldrich syndrome.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1014
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- Publication type:
- Article
3
Living with achondroplasia: attitudes toward population screening and correlation with quality of life.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1003, doi. 10.1002/pd.743
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- Publication type:
- Article
4
Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 981, doi. 10.1002/pd.742
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- Publication type:
- Article
5
Congenital cystic adenomatoid malformation: accuracy of prenatal diagnosis, prevalence and outcome in a general population.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 997, doi. 10.1002/pd.739
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- Publication type:
- Article
6
Chorioangioma and its severe infantile sequelae: case report.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 976, doi. 10.1002/pd.738
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- Publication type:
- Article
7
Prenatal imaging of facial clefts by magnetic resonance imaging with emphasis on the posterior palate.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 970, doi. 10.1002/pd.737
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- Publication type:
- Article
8
Transcervical fetoscopic diagnosis of structural defects in four first-trimester monochorionic twin intrauterine deaths.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 964, doi. 10.1002/pd.736
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- Publication type:
- Article
9
Predicting complications of pregnancy with first-trimester maternal serum free-βhCG, PAPP-A and inhibin-A.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 990, doi. 10.1002/pd.735
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- Publication type:
- Article
10
Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 959, doi. 10.1002/pd.734
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- Publication type:
- Article
11
Mosaic trisomy 13 on chorionic villi in a fetus with body wall complex: fortuitous association or pathogenic hypothesis?
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1021, doi. 10.1002/pd.730
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- Publication type:
- Article
12
Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian population.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1023, doi. 10.1002/pd.731
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- Publication type:
- Article
13
Increased nuchal translucency and congenital heart defects in a low-risk population.
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- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 985, doi. 10.1002/pd.721
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- Publication type:
- Article
14
Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1019, doi. 10.1002/pd.725
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- Publication type:
- Article
15
CGH analysis in a cohort of 17 chromosomally normal fetuses with an increased nuchal translucency.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1017, doi. 10.1002/pd.677
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- Publication type:
- Article
16
Current awareness in prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 12, p. 1027, doi. 10.1002/pd.536
- Publication type:
- Article