X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22

Author:

M�chler M.,Frey D.,Gal A.,Orth U.,Wienker T. F.,Fanconi A.,Schmid W.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference24 articles.

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3. Baas F, Bikker H, van Ommen GJB, De Vijlder JJM (1984) Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele. Hum Genet 67:301?305

4. Bakker E, Hofker MH, Goor N, Mandel JL, Wrogemann K, Davies KE, Kunkel LM, Willard HF, Fenton WA, Sandkuyl L, Majoor-Krakauer D, Essen AJV, Jahoda MGJ, Sachs ES, van Ommen GJB, Pearson PL (1985) Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet I:655?658

5. Buckle VJ, Edwards JH, Evans EP, Jonasson JA, Lyon MF, Peters J, Searle AG (1985) Comparative maps of human and mouse X chromosomes. (8th International Workshop on Human Gene Mapping.) Cytogenet Cell Genet 40:594?595

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