The Intrauterine Diagnosis of Hemoglobin Disorders Journal Articles

abstract

• This article presents an overview of the use of fetal blood and DNA for prenatal testing. The molecular organization of the human hemoglobin genes, the structure of human hemoglobins, and the molecular defects of hemoglobinopathies are also discussed.

authors

• Wong, SC
• Ali, Mahmoud
• Benzie, R

status

• published 

publication date

• June 1984

has subject area

• 1103 Clinical Sciences (FoR)
• 1114 Paediatrics and Reproductive Medicine (FoR)
• Amniotic Fluid (MeSH)
• Anemia, Sickle Cell (MeSH)
• Carrier State (MeSH)
• Chromosome Mapping (MeSH)
• DNA (MeSH)
• DNA Restriction Enzymes (MeSH)
• Female (MeSH)
• Fetal Blood (MeSH)
• Genetic Counseling (MeSH)
• Hemoglobin, Sickle (MeSH)
• Hemoglobinopathies (MeSH)
• Hemoglobins (MeSH)
• Hemoglobins, Abnormal (MeSH)
• Humans (MeSH)
• Methods (MeSH)
• Pediatrics (Science Metrix)
• Polymorphism, Genetic (MeSH)
• Pregnancy (MeSH)
• Prenatal Diagnosis (MeSH)
• Thalassemia (MeSH)

published in

• Clinics in Perinatology  Journal

keywords

• Amniotic Fluid
• Anemia, Sickle Cell
• Carrier State
• Chromosome Mapping
• DNA
• DNA Restriction Enzymes
• Female
• Fetal Blood
• Genetic Counseling
• Hemoglobin, Sickle
• Hemoglobinopathies
• Hemoglobins
• Hemoglobins, Abnormal
• Humans
• Methods
• Polymorphism, Genetic
• Pregnancy
• Prenatal Diagnosis
• Thalassemia

Digital Object Identifier (DOI)

• 10.1016/s0095-5108(18)30921-7

PubMed ID

• 6086205

start page

• 283

end page

• 308

volume

• 11

issue

• 2