92 research outputs found
Innovation of prenatal genetic diagnostics in relation to improvement of care.
Contains fulltext :
74947.pdf (Publisher’s version ) (Open Access)RU Radboud Universiteit Nijmegen, 02 maart 2010Promotor : Geurts van Kessel, A.H.M. Co-promotor : Smits, A.P.T.224 p
Incidental findings of sex chromosome aneuploidies in routine prenatal diagnostic procedures
Item does not contain fulltextRadboud Universiteit Nijmegen, 16 januari 2013Promotores : Braat, D.D.M., Leeuwen, E. van Co-promotores : Smits, A.P.T., Verhaak, C.M
The fragile X syndrome: genetic and diagnostic aspects
Item does not contain fulltextKatholieke Universiteit Nijmegen, 18 april 1996Promotores : Ropers, H.H., Oost, B.A. van, Smeets, D.F.C.M.152 p
The fragile X syndrome: genetic and diagnostic aspects
Contains fulltext :
mmubn000001_219285284.pdf (Publisher’s version ) (Open Access)Promotores : V.[=H.H.] Ropers, B. van Oost en D. SmeetsVII, 152 p
Incidental findings of sex chromosome aneuploidies in routine prenatal diagnostic procedures
Risk estimate for fragile X- associated primary ovarian insufficiency: genetic, environmental and reproductive factors
Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: a pilot study
Considering factors affecting the parental decision to abort after a prenatal diagnosis of a sex chromosome abnormality.
Alfafoetoprotene in vruchtwater voor de detectie van neuralebuisdefecten: beperkte meerwaarde boven de 20-weken-echo; retrospectief onderzoek
Alfafoetoprotene in vruchtwater voor de detectie van neuralebuisdefecten: beperkte meerwaarde boven de 20-weken-echo; retrospectief onderzoek
Contains fulltext :
69642.pdf (Publisher’s version ) (Closed access
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