X-CHROMOSOME-SPECIFIC PROBE DX13 FOR CARRIER DETECTION AND FIRST TRIMESTER PRENATAL DIAGNOSIS IN HAEMOPHILIA A-Reference-Cited by-同舟云学术

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X-CHROMOSOME-SPECIFIC PROBE DX13 FOR CARRIER DETECTION AND FIRST TRIMESTER PRENATAL DIAGNOSIS IN HAEMOPHILIA A

Published:1984-12 Issue:8414 Volume:324 Page:1269-1270
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Tønnesen T.,Søndergaard F.,Mikkelsen M.,Davies K.E.,Old J.,Winter R.M.,Hauge M.

Publisher

Elsevier BV

Subject

General Medicine

Reference2 articles.

1. A clinically useful DNA probe closely linked to haemophilia A;Harper;Lancet,1984

2. Prenatal diagnosis of sickle-cell anemia in the first trimester of pregnancy;Goossens;N Engl J Med,1983

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hemophilia A: Experiences And Attitudes Of Mothers, Sisters, And Daughters;Pediatric Hematology and Oncology;1994-01

2. Carrier detection in Japanese haemophilia a families using factor VIII gene probe (F8A) and the gene-linked ST 14-1 probe;Japanese journal of human genetics;1987-09

3. HAEMOPHILIA A: TWO RECOMBINATIONS DETECTED WITH PROBE Stl4;The Lancet;1986-08

4. Clinical applications of gene probes in human genetic disease, malignancy, and infectious disease;Clinica Chimica Acta;1986-05

5. Diagnosis of genetic disease using recombinant DNA;Human Genetics;1986-05

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