Prenatal diagnosis of haemoglobin disorders by cordocentesis at 12 weeks' gestation

Prenatal diagnosis of haemoglobin disorders is accepted to be a useful procedure to avoid births of infants with homozygous diseases. Advances in sampling and molecular techniques, such as polymerase chain reaction (PCR) and chorionic villus sampling (CVS), have made earlier and safer first‐trimeste...

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Veröffentlicht in:	Prenatal diagnosis 1991-12, Vol.11 (12), p.899-904
Hauptverfasser:	Di Trapani, F., Marino, M., D'Alcamo, E., Abate, I., D'Agostino, S., Lauricella, S., Musicò, M., Orlandi, F., Sammarco, P., Maggio, A., Modell, B.
Format:	Artikel
Sprache:	eng
Schlagworte:	beta -thalassemia Biological and medical sciences Early cordocentesis Female Fetal Blood - chemistry Follow-Up Studies Genotype Globin chain synthesis Gynecology. Andrology. Obstetrics Hemoglobin A - analysis Humans Management. Prenatal diagnosis Medical sciences Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Pregnancy Pregnancy Trimester, First Pregnancy. Fetus. Placenta Prenatal diagnosis Prenatal Diagnosis - methods Reproducibility of Results Thalassemia - diagnosis Thalassemia - genetics β-Thalassaemia β/γ ratios
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