-
1
-
-
0025307919
-
Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification
-
Handyside AH, Kontogianni EH, Hardy K, Winston RML. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature 1990;344:768-70.
-
(1990)
Nature
, vol.344
, pp. 768-770
-
-
Handyside, A.H.1
Kontogianni, E.H.2
Hardy, K.3
Winston, R.M.L.4
-
3
-
-
0032494677
-
Genetische diagnostiek bij IVF-embryo's: Eerste ervaringen met 'preïmplantatiegenetische diagnostiek' in Nederland
-
Die-Smulders CEM de, Geraedts JPM, Dreesen JCFM, Coonen E, Land JA. Genetische diagnostiek bij IVF-embryo's: eerste ervaringen met 'preïmplantatiegenetische diagnostiek' in Nederland. Ned Tijdschr Geneeskd 1998;142:2241-4.
-
(1998)
Ned Tijdschr Geneeskd
, vol.142
, pp. 2241-2244
-
-
De Die-Smulders, C.E.M.1
Geraedts, J.P.M.2
Dreesen, J.C.F.M.3
Coonen, E.4
Land, J.A.5
-
4
-
-
10644278830
-
Planningsbesluit klinisch genetisch onderzoek en erfelijkheidsadvisering
-
Planningsbesluit klinisch genetisch onderzoek en erfelijkheidsadvisering. Staatscourant 2003;16:11.
-
(2003)
Staatscourant
, vol.16
, pp. 11
-
-
-
6
-
-
0004255538
-
-
Publicatienr 1998/08. Den Haag: Gezondheidsraad
-
Commissie Herziening Planningsbesluit IVF. IVF: afrondende advisering. Publicatienr 1998/08. Den Haag: Gezondheidsraad; 1998.
-
(1998)
IVF Afrondende Advisering
-
-
-
7
-
-
0033999881
-
Preimplantation genetic diagnosis of a reciprocal translocation t(3;11)(q27.3;q24.3) in siblings
-
Coonen E, Martini E, Dumoulin JCM, Hollanders-Crombach HTM, Die-Smulders CEM de, Geraedts JPM, et al. Preimplantation genetic diagnosis of a reciprocal translocation t(3;11)(q27.3;q24.3) in siblings. Mol Hum Reprod 2000;6:199-206.
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 199-206
-
-
Coonen, E.1
Martini, E.2
Dumoulin, J.C.M.3
Hollanders-Crombach, H.T.M.4
De Die-Smulders, C.E.M.5
Geraedts, J.P.M.6
-
8
-
-
0031663165
-
Preimplantation genetic diagnosis of spinal muscular atrophy
-
Dreesen JC, Bras M, Die-Smulders C de, Dumoulin JC, Cobben JM, Evers JL, et al. Preimplantation genetic diagnosis of spinal muscular atrophy. Mol Hum Reprod 1998;4:881-5.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 881-885
-
-
Dreesen, J.C.1
Bras, M.2
De Die-Smulders, C.3
Dumoulin, J.C.4
Cobben, J.M.5
Evers, J.L.6
-
9
-
-
0034101415
-
Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis
-
Dreesen JC, Jacobs LJ, Bras M, Herbergs J, Dumoulin JC, Geraedts JP, et al. Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis. Mol Hum Reprod 2000;6:391-6.
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 391-396
-
-
Dreesen, J.C.1
Jacobs, L.J.2
Bras, M.3
Herbergs, J.4
Dumoulin, J.C.5
Geraedts, J.P.6
-
10
-
-
0035935216
-
PGD in the lab for triplet repeat diseases - Myotonic dystrophy, Huntington's disease and Fragile-X syndrome
-
Sermon K, Seneca S, Rycke M de, Goossens V, Velde H van de, Vos A de, et al. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome. Mol Cell Endocrinol 2001;183 Suppl 1:S77-85.
-
(2001)
Mol Cell Endocrinol
, vol.183
, Issue.SUPPL. 1
-
-
Sermon, K.1
Seneca, S.2
De Rycke, M.3
Goossens, V.4
Van De Velde, H.5
De Vos, A.6
-
11
-
-
1042280359
-
Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)(n) repeat detection
-
Drüsedau M, Dreesen JCFM, Die-Smulders CEM de, Hardy K, Bras M, Dumoulin JCM, et al. Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)(n) repeat detection. Mol Hum Reprod 2004;10:71-5.
-
(2004)
Mol Hum Reprod
, vol.10
, pp. 71-75
-
-
Drüsedau, M.1
Dreesen, J.C.F.M.2
De Die-Smulders, C.E.M.3
Hardy, K.4
Bras, M.5
Dumoulin, J.C.M.6
-
12
-
-
0037225240
-
Strategies and outcomes of the first 100 cycles of preimplantation genetic diagnosis at the Guy's and St. Thomas' Center
-
Pickering S, Polidoropoulos N, Caller J, Scriven P, Ogilvie CM, Braude P. Strategies and outcomes of the first 100 cycles of preimplantation genetic diagnosis at the Guy's and St. Thomas' Center. Fertil Steril 2003;79:81-90.
-
(2003)
Fertil Steril
, vol.79
, pp. 81-90
-
-
Pickering, S.1
Polidoropoulos, N.2
Caller, J.3
Scriven, P.4
Ogilvie, C.M.5
Braude, P.6
-
13
-
-
0001043863
-
ESHRE Preimplantation genetic diagnosis consortium: Data collection III (May 2001)
-
ESHRE PGD Consortium Steering Committee. ESHRE Preimplantation genetic diagnosis consortium: data collection III (May 2001). Hum Reprod 2002;17:233-40.
-
(2002)
Hum Reprod
, vol.17
, pp. 233-240
-
-
-
14
-
-
0041520974
-
Preimplantation genetic diagnosis of chromosome abnormalities: Implications from the outcome for couples with chromosomal rearrangements
-
Simopoulau M, Harper JC, Fragouli E, Mantzouratou A, Speyer BE, Serhal P, et al. Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements. Prenat Diagn 2003;23:652-62.
-
(2003)
Prenat Diagn
, vol.23
, pp. 652-662
-
-
Simopoulau, M.1
Harper, J.C.2
Fragouli, E.3
Mantzouratou, A.4
Speyer, B.E.5
Serhal, P.6
-
15
-
-
0036898687
-
Myotonic dystrophy and the heart
-
Pelargonio G, dello Russo A, Sanna T, de Martino G, Bellocci F. Myotonic dystrophy and the heart. Heart 2002;88:665-70.
-
(2002)
Heart
, vol.88
, pp. 665-670
-
-
Pelargonio, G.1
Dello Russo, A.2
Sanna, T.3
De Martino, G.4
Bellocci, F.5
-
16
-
-
0032412865
-
Non-disclosure preimplantation genetic diagnosis for Huntington's disease; Practical and ethical dilemma's
-
Braude PR, Wert GM de, Evers-Kieboom G, Pettigrew RA, Geraedts JG. Non-disclosure preimplantation genetic diagnosis for Huntington's disease; practical and ethical dilemma's. Prenat Diagn 1998;18:1422-6.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1422-1426
-
-
Braude, P.R.1
De Wert, G.M.2
Evers-Kieboom, G.3
Pettigrew, R.A.4
Geraedts, J.G.5
-
18
-
-
10644261371
-
Preimplantation genetic diagnosis is a limited reproductive option for fragile X carriers
-
Die-Smulders CEM de, Land JA, Dreesen JCFM, Geraedts JPM, Dunselman GAJ, Evers JLH. Preimplantation genetic diagnosis is a limited reproductive option for fragile X carriers. Hum Reprod 2001;16A:P-214.
-
(2001)
Hum Reprod
, vol.16 A
-
-
De Die-Smulders, C.E.M.1
Land, J.A.2
Dreesen, J.C.F.M.3
Geraedts, J.P.M.4
Dunselman, G.A.J.5
Evers, J.L.H.6
-
19
-
-
0035104929
-
Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives
-
Hundscheid RDL, Braat DDM, Kiemeney LALM, Smits APT, Thomas CMG. Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives. Hum Reprod 2001;16:457-62.
-
(2001)
Hum Reprod
, vol.16
, pp. 457-462
-
-
Hundscheid, R.D.L.1
Braat, D.D.M.2
Kiemeney, L.A.L.M.3
Smits, A.P.T.4
Thomas, C.M.G.5
-
20
-
-
0037038839
-
Resultaten van in-vitrofertilisatie in Nederland, 1996-2000
-
Kremer JAM, Beekhuizen W, Bots RSGM, Braat DDM, Dop PA van, Jansen CAM, et al. Resultaten van in-vitrofertilisatie in Nederland, 1996-2000. Ned Tijdschr Geneeskd 2002;146:2358-63.
-
(2002)
Ned Tijdschr Geneeskd
, vol.146
, pp. 2358-2363
-
-
Kremer, J.A.M.1
Beekhuizen, W.2
Bots, R.S.G.M.3
Braat, D.D.M.4
Van Dop, P.A.5
Jansen, C.A.M.6
-
21
-
-
0033842601
-
The Brussels' experience of more than 5 years of clinical preimplantation genetic diagnosis
-
Vandervorst M, Staessen C, Sermon K, Vos A de, Velde H van de, et al. The Brussels' experience of more than 5 years of clinical preimplantation genetic diagnosis. Hum Reprod update 2000;6:364-73.
-
(2000)
Hum Reprod Update
, vol.6
, pp. 364-373
-
-
Vandervorst, M.1
Staessen, C.2
Sermon, K.3
De Vos, A.4
Van De Velde, H.5
-
22
-
-
0023179182
-
Increased monozygotic twinning rate after ovulation induction
-
Derom C, Vlietinck R, Derom R, Berghe H van den, Thiery M. Increased monozygotic twinning rate after ovulation induction. Lancet 1987;1(8544)1:1236- 8.
-
(1987)
Lancet
, vol.1
, Issue.8544
, pp. 1
-
-
Derom, C.1
Vlietinck, R.2
Derom, R.3
Van Den Berghe, H.4
Thiery, M.5
|