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September 1, 1988British Journal of Haematology

Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms

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Authors

PMPeter MoodieUniversity of AucklandMLM. B. LiddellUniversity of WalesIPI R PeakeNational Institutes of Health

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Moodie et al. (1988) studied this question.

synapsesocial.com/papers/6aa5f3174bcbe4818eeeb548https://doi.org/10.1111/j.1365-2141.1988.tb02437.x
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A1986 · 132 citations
  2. 2Application of molecular genetics to prenatal diagnosis and carrier detection in the hemophilias: some limitations1985 · 40 citations
  3. 3Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia B1986 · 19 citations
  4. 4An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA Sequences1987 · 805 citations