Quantitative Real-Time PCR Assay for Rapid Identification of Deletion Carriers in Hemophilia-Reference-Cited by-同舟云学术

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Quantitative Real-Time PCR Assay for Rapid Identification of Deletion Carriers in Hemophilia

Published:2004-07-01 Issue:7 Volume:50 Page:1269-1270
ISSN:0009-9147
Container-title:Clinical Chemistry
language:en
Short-container-title:

Author:

Costa Catherine¹²,Jouannic Jean-Marie³,Stieltjes Nathalie⁴,Costa Jean-Marc⁵,Girodon Emmanuelle¹²,Goossens Michel¹²

Affiliation:

1. Laboratoire de, Génétique Moléculaire, Centre Hospitalier Universitaire, Henri Mondor AP-HP, Créteil, France

2. INSERM U468, Créteil, France

3. Service de Médecine Fœtale, Institut de Puériculture de Paris, Paris, France

4. Centre de Traitement des Hémophiles, Groupe Hospitalier Cochin, Saint Vincent de Paul, Paris, France, and

5. Centre de Diagnostic Prénatal, Hôpital Américain de Paris, Neuilly/Seine, France

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

Link

http://academic.oup.com/clinchem/article-pdf/50/7/1269/32732940/clinchem1269.pdf

Reference4 articles.

1. A 20.7 kb Deletion within the Factor VIII Gene Associated with LINE-1 Element Insertion

2. Prenatal Detection by Real-Time Quantitative PCR and Characterization of a New CFTR Deletion, 3600+15kbdel5.3kb (or CFTRdele19)

3. The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism

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2. Manganese-Induced Neurotoxicity through Impairment of Cross-Talk Pathways in Human Neuroblastoma Cell Line SH-SY5Y Differentiated with Retinoic Acid;Toxics;2021-12-09

3. Manganese-induced cellular disturbance in the baker’s yeast, Saccharomyces cerevisiae with putative implications in neuronal dysfunction;Scientific Reports;2019-04-25

4. Reliable and cost-effective approach for diagnosis of heterozygousF8/F9large deletions by quantitative real-time PCR;Haemophilia;2015-03-10

5. Identification of deletion carriers in hemophilia B: quantitative real-time polymerase chain reaction or multiple ligation probe amplification;Translational Research;2009-03

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