Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Cryptorchidism and WT1[original query] |
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| Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004 Oct 22 (20): 4140-6. Little Suzanne E, Hanks Sandra P, King-Underwood Linda, Jones Chris, Rapley Elizabeth A, Rahman Nazneen, Pritchard-Jones Kat |
| Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex development. The Journal of clinical endocrinology and metabolism 2011 Jul 96 (7): E1131-6. Köhler B, Biebermann H, Friedsam V, Gellermann J, Maier R F, Pohl M, Wieacker P, Hiort O, Grüters A, Krude |
| The mutational spectrum of WT1 in male infertility. The Journal of urology 2015 May 193 (5): 1709-15. Seabra Catarina M, Quental Sofia, Lima Ana C, Carvalho Filipa, Gonçalves João, Fernandes Susana, Pereira Iris, Silva Júlia, Marques Patrícia I, Sousa Mário, Barros Alberto, Seixas Susana, Amorim António, Lopes Alexandra |
| New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report. Medicine 2021 6 100 (19): e25864. Akramov Nail R, Shavaliev Rafael F, Osipova Ilsiya |
- Page last reviewed:Feb 1, 2024
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