Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families

Author:

Thakker R.V.,Davies K.E.,Read A.P.,Tippett P.,Wooding C.,Flint T.,Woob S.,Kruse T.A.,Whyte M.P.,O'Riordan J.L.H.

Publisher

Elsevier BV

Subject

Genetics

Reference29 articles.

1. Anonymous X-chromosomal probes revealing DNA polymorphisms one of which is a deletion of more than 3kb;Ahrens;Cytogenet. Cell Genet.,1985

2. An anonymous X-chromosomal clone identifying a frequent RFLP at Xp21–22 (HGM8 Provisional No. DXS207);Ahrens;Nucleic Acids Res.,1986

3. Close linkage between X-linked hypophosphataemia and DXS207 defined by the DNA probe pPA4B;Albertsen;Cytogenet. Cell Genet.,1987

4. Construction of a genetic linkage map in Man using restriction fragment length polymorphisms;Botstein;Amer. J. Hum. Genet.,1980

5. Etude critique de l'hypophosphatemic pour l'etude genetique du rachitisme vitamino-resistant hypophosphatemique familial;Briard-Buillemot;Arch. Fr. Pediatr.,1972

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2. Heritable Renal Phosphate Wasting Disorders;Genetics of Bone Biology and Skeletal Disease;2013

3. Familial Hypophosphatemia and Related Disorders;Pediatric Bone;2012

4. Rickets;Atlas of Genetic Diagnosis and Counseling;2012

5. Clinical Disorders of Phosphate Homeostasis;Vitamin D;2011

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