Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13

Author:

Toren Amos,Amariglio Ninette,Rozenfeld-Granot Galit,Simon Amos J.,Brok-Simoni Frida,Pras Elon,Rechavi Gideon

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference34 articles.

1. Hereditary familial congenital hemorrhagic nephritis;Alport;Br J Med,1927

2. Alport syndrome and diffuse leiomyomatosis: deletions in the 5′ end of the COL4A5 gene;Antignac;Kidney Int,1992

3. Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43;Barrat;Am J Hum Genet,1996

4. Thrombocytopenia, macrothrombopathia, nephritis and deafness;Bernheim;Am J Med,1976

5. The genes coding for human pro alpha 1(IV) and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13;Boyd;Am J Hum Genet,1988

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