Genetic and physical mapping of Xq24–q26 markers flanking the Lowe oculocerebrorenal syndrome

Author:

Reilly Dorothy Silver,Lewis Richard Alan,Nussbaum Robert L.

Publisher

Elsevier BV

Subject

Genetics

Reference43 articles.

1. Oculocerebrorenal syndrome: A review;Abbassi;Amer. J. Dis. Child,1968

2. A strategy to reveal high-frequency RFLPs along the human X chromosome;Aldridge;Amer. J. Hum. Genet,1984

3. Arthropathy of Lowe's (oculocerebrorenal) syndrome;Athreya;Arthritis Rheum,1983

4. Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26-qter;Boggs;Somatic Cell Mol. Genet,1984

5. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy;Boyd;Cytogenet. Cell Genet,1988

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