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D F Smeets

Showing results (11-20 of 51) with videos related to

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Immunodeficiency|January 1, 1993
Variants of Nijmegen breakage syndrome and ataxia telangiectasiaC M Weemaes, D F Smeets, M Horstink, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie diseaseA Gal, B Wieringa, D F Smeets, et al.
Annales De Genetique|January 1, 1997
A phenotypical male infant with 46,X,der(Y)t(X;Y)(?;p11) de novoL C Govaerts, J M Draaisma, M vd Blij-Philipsen, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Evidence for specificity of the DA/DAPI techniqueG F Merkx, A H Hopman, A C Akkermans-Scholten, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance estimate of the fra(X) gene using Pointer versus direct estimateA F de Haan, A P Smits, D F Smeets, et al.
Journal of Medical Genetics|October 1, 1994
Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, et al.
American Journal of Medical Genetics|March 1, 1992
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalisB A Semmekrot, A Haraldsson, C M Weemaes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1994
Late-onset ataxia telangiectasia in two brothers presenting with juvenile resting tremorJ A Hiel, C M Weemaes, D F Smeets, et al.
Urology|February 22, 2001
Absence of karyotype abnormalities in patients with familial urothelial cell carcinomaK K Aben, M V Macville, D F Smeets, et al.
Human Genetics|September 1, 1994
ICF syndrome: a new case and review of the literatureD F Smeets, U Moog, C M Weemaes, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Immunodeficiency|January 1, 1993
Variants of Nijmegen breakage syndrome and ataxia telangiectasiaC M Weemaes, D F Smeets, M Horstink, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie diseaseA Gal, B Wieringa, D F Smeets, et al.
Annales De Genetique|January 1, 1997
A phenotypical male infant with 46,X,der(Y)t(X;Y)(?;p11) de novoL C Govaerts, J M Draaisma, M vd Blij-Philipsen, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Evidence for specificity of the DA/DAPI techniqueG F Merkx, A H Hopman, A C Akkermans-Scholten, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance estimate of the fra(X) gene using Pointer versus direct estimateA F de Haan, A P Smits, D F Smeets, et al.
Journal of Medical Genetics|October 1, 1994
Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, et al.
American Journal of Medical Genetics|March 1, 1992
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalisB A Semmekrot, A Haraldsson, C M Weemaes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1994
Late-onset ataxia telangiectasia in two brothers presenting with juvenile resting tremorJ A Hiel, C M Weemaes, D F Smeets, et al.
Urology|February 22, 2001
Absence of karyotype abnormalities in patients with familial urothelial cell carcinomaK K Aben, M V Macville, D F Smeets, et al.
Human Genetics|September 1, 1994
ICF syndrome: a new case and review of the literatureD F Smeets, U Moog, C M Weemaes, et al.
Pageof 6