Found: 17
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Second-trimester maternal urinary gonadotrophin peptide screening for fetal Down syndrome in Asian women.
- Published in:
- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1101, doi. 10.1002/(SICI)1097-0223(199712)17:12<1101::AID-PD195>3.0.CO;2-S
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- Article
Screening for Down syndrome using urine hCG free β-subunit in the second trimester of pregnancy.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1107, doi. 10.1002/(SICI)1097-0223(199712)17:12<1107::AID-PD199>3.0.CO;2-A
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- Article
Trends in the use of prenatal diagnosis in New York State and the impact of biochemical screening on the detection of Down syndrome: 1984-1993.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1113, doi. 10.1002/(SICI)1097-0223(199712)17:12<1113::AID-PD200>3.0.CO;2-7
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- Article
Combining β-core fragment and total oestriol measurements to test for Down syndrome pregnancies.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1125, doi. 10.1002/(SICI)1097-0223(199712)17:12<1125::AID-PD201>3.0.CO;2-#
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- Article
Levels of urinary beta-core fragment, total oestriol, and the ratio of the two in second-trimester screening for Down syndrome.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1135, doi. 10.1002/(SICI)1097-0223(199712)17:12<1135::AID-PD217>3.0.CO;2-E
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- Article
Limb reduction defects in fetuses with homozygous α-thalassaemia-1.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1143, doi. 10.1002/(SICI)1097-0223(199712)17:12<1143::AID-PD204>3.0.CO;2-N
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- Article
First prenatal diagnosis by mutation analysis in a family with Sjögren-Larsson syndrome.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1147, doi. 10.1002/(SICI)1097-0223(199712)17:12<1147::AID-PD206>3.0.CO;2-D
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- Article
Analysis of cystic hygroma, ascitic, and pleural fluids by conventional lymphocyte culture and fluorescent in situ hybridization.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1151, doi. 10.1002/(SICI)1097-0223(199712)17:12<1151::AID-PD208>3.0.CO;2-A
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- Article
Characterization of fetal haematopoietic progenitors circulating in maternal blood of seven aneuploid pregnancies.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1159, doi. 10.1002/(SICI)1097-0223(199712)17:12<1159::AID-PD250>3.0.CO;2-L
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- Article
True fetal mosaicism of an isochromosome of the long arm of a chromosome 20: the dilemma persists.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1171, doi. 10.1002/(SICI)1097-0223(199712)17:12<1171::AID-PD181>3.0.CO;2-K
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- Article
Prenatal diagnosis of Klippel-Trénaunay-Weber syndrome as a cause for in utero heart failure and severe postnatal sequelae.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1176, doi. 10.1002/(SICI)1097-0223(199712)17:12<1176::AID-PD202>3.0.CO;2-H
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- Article
The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22-24).
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1181, doi. 10.1002/(SICI)1097-0223(199712)17:12<1181::AID-PD205>3.0.CO;2-A
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- Article
Maternal serum screening abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia.
- Published in:
- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1187, doi. 10.1002/(SICI)1097-0223(199712)17:12<1187::AID-PD203>3.0.CO;2-A
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- Article
Oligosaccharide variants of hCG-related molecules: potential screening markers for Downs syndrome.
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- Prenatal Diagnosis, 1997, v. 17, n. 12, p. 1188, doi. 10.1002/(SICI)1097-0223(199712)17:12<1188::AID-PD222>3.0.CO;2-A
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- Article
The aetiology and management of twin-twin transfusion syndrome.
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- 1997
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- Publication type:
- journal article
Diagnosis and management of early non-immune hydrops fetalis.
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- 1997
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- Publication type:
- journal article
Prenatal diagnosis of congenital heart disease.
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- 1997
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- Publication type:
- journal article