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Results: 1-9 |
Results: 9
A genome-wide scan for preeclampsia in the Netherlands
Authors: Lachmeijer, AMA Arngrimsson, R Bastiaans, EJ Frigge, ML Pals, G Sigurdardottir, S Stefansson, H Palsson, B Nicolae, D Kong, A Aarnoudse, JG Gulcher, JR Dekker, GA ten Kate, LP Stefansson, K
Citation: Ama. Lachmeijer et al., A genome-wide scan for preeclampsia in the Netherlands, EUR J HUM G, 9(10), 2001, pp. 758-764
Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF)
Authors: Henneman, L Bramsen, I Van Os, TAM Reuling, IEW Heyerman, HGM van der Laag, J van der Ploeg, HM ten Kate, LP
Citation: L. Henneman et al., Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF), PRENAT DIAG, 21(1), 2001, pp. 1-9
Polymorphisms in the tumor necrosis factor and lymphotoxin-alpha gene region and preeclampsia
Authors: Lachmeijer, AMA Crusius, JBA Pals, G Dekker, GA Arngrimsson, R ten Kate, LP
Citation: Ama. Lachmeijer et al., Polymorphisms in the tumor necrosis factor and lymphotoxin-alpha gene region and preeclampsia, OBSTET GYN, 98(4), 2001, pp. 612-619
Participation preconceptional carrier couple screening: characteristics, attitudes, and knowlege of both partners
Authors: Henneman, L Bramsen, I van der Ploeg, HM Ader, HJ van der Horst, HE Gille, JJP ten Kate, LP
Citation: L. Henneman et al., Participation preconceptional carrier couple screening: characteristics, attitudes, and knowlege of both partners, J MED GENET, 38(10), 2001, pp. 695-703
Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia
Authors: Lachmeijer, AMA Arngrimsson, R Bastiaans, EJ Pals, G ten Kate, LP de Vries, JIP Kostense, PJ Aarnoudse, JG Dekker, GA
Citation: Ama. Lachmeijer et al., Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia, AM J OBST G, 184(3), 2001, pp. 394-402
Efficacy of cascade testing for fragile X syndrome
Authors: Wildhagen, MF van Os, TAM Polder, JJ ten Kate, LP Habbema, JDF
Citation: Mf. Wildhagen et al., Efficacy of cascade testing for fragile X syndrome, J MED SCREE, 6(2), 1999, pp. 70-76
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome
Authors: Kohlhase, J Taschner, PEM Burfeind, P Pasche, B Newman, B Blanck, C Breuning, MH ten Kate, LP Maaswinkel-Mooy, P Mitulla, B Seidel, J Kirkpatrick, SJ Pauli, RM Wargowski, DS Devriendt, K Proesmans, W Gabrielli, O Coppa, GV Wesby-van Swaay, E Trembath, RC Schinzel, AA Reardon, W Seemanova, E Engel, W
Citation: J. Kohlhase et al., Molecular analysis of SALL1 mutations in Townes-Brocks syndrome, AM J HU GEN, 64(2), 1999, pp. 435-445
Concordance for pre-eclampsia in monozygous twins
Authors: Lachmeijer, AMA Aarnoudse, JG ten Kate, LP Pals, G Dekker, GA
Citation: Ama. Lachmeijer et al., Concordance for pre-eclampsia in monozygous twins, BR J OBST G, 105(12), 1998, pp. 1315-1317
Screening for cystic fibrosis and its evaluation
Authors: Wildhagen, MF ten Kate, LP Habbema, JDF
Citation: Mf. Wildhagen et al., Screening for cystic fibrosis and its evaluation, BR MED B, 54(4), 1998, pp. 857-875
Risultati: 1-9 |