| 1 | DDS, WT1, CDH
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| Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation.
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| Antonius T, van Bon B, Eggink A, van der Burgt I, Noordam K, van Heijst A.
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| Am J Med Genet A 146(4):496-9. 2008
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| 2 | DDS, WT1
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| Murine Denys-Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosis.
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| Patek CE, Fleming S, Miles CG, Bellamy CO, Ladomery M, Spraggon L, Mullins J, Hastie ND, Hooper ML.
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| Hum Mol Genet 12(18):2379-94. Epub 2003 Jul 22. 2003
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| 3 | DDS, GBGT1, WT1
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| Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation.
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| Hammes A, Guo JK, Lutsch G, Leheste JR, Landrock D, Ziegler U, Gubler MC, Schedl A.
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| Cell 106(3):319-29. 2001
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| 4 | DDS, WAGR
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| Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.
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| Kohler B, et al.
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| Pediatr Res 45(2):187-90. 1999
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| 5 | DDS
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| A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome.
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| Patek CE, et al.
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| Proc Natl Acad Sci U S A 96(6):2931-6. 1999
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| 6 | NR0B2, DDS, NR5A1, WT1
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| Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression.
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| Nachtigal MW, et al.
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| Cell 93 : 445-454. 1998
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| 7 | DDS
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| X-linked Dystonia-Deafness syndrome.
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| Hayes MW, Ouvrier RA, Evans W, Somerville E, Morris JG.
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| Mov Disord 13(2):303-8. 1998
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| 8 | DDS, GBGT1, WT1
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| Sugar and spice and all things splice?
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| Van Heyningen V.
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| Nat Genet 17(4):367-8. No abstract available. 1997
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| 9 | DDS
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| Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndrome.
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| Turleau C, et al.
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| Hum Genet 75 : 81-83. 1987
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