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Browsing by Author Verloes, A.
Showing results 1 to 3 of 3
| Full Text | Issue Date | Title | Author(s) | | 2006 | Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinical classification of the so-called Ohdo syndrome, and delineation of two new BMR syndromes, one X-linked and one autosomal recessive. | Verloes, A.; Bremond-Gignac, D.; Isidor, B., et al |
| 2011 | Clinical utility gene card for: CHARGE syndrome. | Blake, K.; Ravenswaaij-Arts, C.M.A. van; Hoefsloot, L.H., et al |
| 2012 | De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome | Riviere, J.B.; Bon, B.W. van; Hoischen, A., et al |
Showing results 1 to 3 of 3
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