Linkage of adrenoleukodystrophy to a polymorphic DNA probe
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference28 articles.
1. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28
2. First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe
3. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
4. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.
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1. Adrenoleukodystrophy in the era of newborn screening;Current Opinion in Endocrinology, Diabetes & Obesity;2020-02
2. X-linked Adrenoleukodystrophy;Colloquium Series on The Genetic Basis of Human Disease;2013-03-25
3. Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidation;Clinical Genetics;2008-06-28
4. Adrenomyeloneuropathie als Ursache eines Morbus Addison;DMW - Deutsche Medizinische Wochenschrift;2008-03-25
5. X-linked adrenoleukodystrophy: Clinical, biochemical and pathogenetic aspects;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2006-12
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