Utility Of The Polymerase Chain Reaction (Pcr) For Prenatal Diagnosis Of Genetic Disease

No abstract is available for this paper.

• Publication year

  1991

• Venue

  Pathology (Sydney)

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.3109/00313029109060817PMID 1745568
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Polymerase chain reaction (PCR) mutagenesis enabling rapid non‐radioactive detection of common β‐thalassaemia mutations in Mediterraneans

  1991cited by this paper
• Experience of a molecular genetics service in prenatal diagnosis by DNA Analysis

  1990cited by this paper
• Identification of the cystic fibrosis gene: genetic analysis.

  1989cited by this paper
• DETECTION AND CHARACTERIZATION OF THE Hb LEPORE (BOSTON) DEFECT BY THE POLYMERASE CHAIN REACTION

  1989cited by this paper
• Identification of the cystic fibrosis gene: genetic analysis

  1989cited by this paper
• Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening

  1989cited by this paper
• Polymerase chain reaction: replication errors and reliability of gene diagnosis.

  1989cited by this paper
• ASSOCIATION OF CONGENITAL PROTEIN C DEFICIENCY AND LATENT MYELOPROLIFERATIVE DISEASE AS CAUSE OF SPLANCHNIC VENOUS THROMBOSIS IN A 34‐YEAR‐OLD WOMAN

  1989cited by this paper
• Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

  1989cited by this paper
• Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

  1988cited by this paper
• The detection of β-globin gene mutations in β-thalassemia using oligonucleotide probes and amplified DNA

  1988cited by this paper
• Fidelity of DNA synthesis by the Thermus aquaticus DNA polymerase.

  1988cited by this paper
• [A simple approach to prenatal diagnosis of beta thalassemia].

  1988cited by this paper
• A simple approach to prenatal diagnosis of beta-thalassemia in a geographic area where multiple mutations occur.

  1988cited by this paper
• The detection of beta-globin gene mutations in beta-thalassemia using oligonucleotide probes and amplified DNA.

  1988cited by this paper
• Detection of sickle cell anaemia and thalassaemias

  1987cited by this paper
• THE PRENATAL DIAGNOSIS OF THALASSAEMIA

  1986cited by this paper
• ANTENATAL DIAGNOSIS OF SEVERE β THALASSEMIA DURING THE FIRST TRIMESTER OF PREGNANCY

  1985cited by this paper
• Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.

  1985cited by this paper
• Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

  1985cited by this paper
• Prenatal Diagnosis of β - Thalassemia

  1983cited by this paper
• Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

  1982cited by this paper
• Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster

  1982cited by this paper

• The Power of Old Hats: Rediscovering Inosine-EpPCR to Create Starting Libraries for Whole-Cell-SELEX

  2025cites this paper
• Genetic Diagnostics as a Basis for Selection of Personalized Therapy for Monogenic Diseases

  2025cites this paper
• Prenatal diagnosis of hemoglobinopathies: from fetoscopy to coelocentesis

  2014cites this paper
• Psychiatric genetics. Future and prospects.

  2003cites this paper
• Combine-ARMS: A Rapid and Cost-Effective Protocol for Molecular Characterization of β-Thalassemia in Malaysia

  2001cites this paper
• Nucleic acid amplification strategies for diagnosis of heritable diseases

  1997cites this paper
• Prenatal diagnosis of Hb Bart's hydrops fetalis in West Malaysia: the identification of the alpha thal 1 defect by PCR based strategies.

  1996cites this paper
• Hydrops fetalis: role of the geneticist.

  1995cites this paper
• Applications of the polymerase chain reaction (PCR) to the diagnosis of pediatric pulmonary disease

  1995cites this paper
• The amplification refractory mutation system (ARMS): A rapid and direct prenatal diagnostic technique for β‐thalassaemia in Singapore

  1994cites this paper
• The amplification refractory mutation system (ARMS): a rapid and direct prenatal diagnostic technique for beta-thalassaemia in Singapore.

  1994cites this paper
• Implications Of Rdna Technology In The Microbiology Laboratory

  1992cites this paper
• Target-dependent amplifiable nucleic acid hybridization probes

  1992cites this paper
• Pathology and laboratory medicine.

  1992cites this paper
• Pathology and laboratory medicine.

  1991cites this paper