Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus

Author:

Knoers N.,van der Heyden H.,van Oost B.A.,Monnens L.,Willems J.,Ropers H.H.

Publisher

Elsevier BV

Subject

Genetics

Reference30 articles.

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3. RFLP for linkage analysis of fragile X syndrome;Brown;Lancet,1987

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1. Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study;European Journal of Pediatrics;2015-04-23

2. Polyuria and Diabetes Insipidus;Seldin and Giebisch's The Kidney;2013

3. Polyuria and Diabetes Insipidus;Seldin and Giebisch's The Kidney;2008

4. Diabetes Insipidus in Pediatrics;Hormone Replacement Therapy;1999

5. Diversity of nephrogenic diabetes insipidus mutations and importance of early recognition and treatment;Clinical and Experimental Nephrology;1998-12

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