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development germ cells patient gonad sox 9 gonadal foxl 2 analysis expression tumor deletion figure protein sex development mutation staining import r hersmus european journal domain testicular testi genetic germ cell tumors differentiation cancer chromosome marker oct 3/4 lesion immunohistochemical gonadal dysgenesis looijenga lh gonadal development journal import european presence sox 9 expression looijenga gb lesion gonadoblastoma sertoli sry mutation wwox gene sequence activity erasmus mc-university tissue center rotterdam identi fied ww domains accumulation disorder 3/4 rotterdam sdr domain factor probe identi type ii gcts genetics sry mutation germ cells /gonocytes figure 3 c panel hersmu australia dysgenesi gonadal tissue pcdna 3-flag lovell-badge r pathol y chromosome number study right granulosa melbourne pcdna precursor research
2 Most Recent Publications
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A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development
(Article)
White, S.J. Hewitt, J.H. Sinclair, A. Turbitt, E. Zwan, Y.G. van der Hersmus, R. Drop, S.L.S. Koopman, P.L. Harley, V.R. Cools, M.B.C.M. Looijenga, L.H.J. |
2012-03-01
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A novel SRY missense mutation affecting nuclear import in a 46,XY female patient with bilateral gonadoblastoma
(Article)
Hersmus, R. Leeuw, B. de Stoop, J.A. Bernard, P. Doorn, H.C. van Brüggenwirth, H.T. Drop, S.L.S. Oosterhuis, J.W. Harley, V.R. Looijenga, L.H.J. |
2009-06-12
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