Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: The importance of enzyme analysis to ascertain true MCAD deficiency
Derks, T. G. J., Boer, T. S., van Assen, A., Bos, T., Ruiter, J., Waterham, H. R., Niezen-Koning, K. E., Wanders, R. J. A., Rondeel, J. M. M., Loeber, J. G., ten Kate, L. P., Smit, G. P. A., Reijngoud, D.-J.
Published in Journal of inherited metabolic disease (01.02.2008)
Published in Journal of inherited metabolic disease (01.02.2008)
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Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF)
Henneman, L., Bramsen, I., Van Os, Th. A. M., Reuling, I. E. W., Heyerman, H. G. M., van der Laag, J., van der Ploeg, H. M., ten Kate, L. P.
Published in Prenatal diagnosis (01.01.2001)
Published in Prenatal diagnosis (01.01.2001)
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TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
Ruijs, Marielle W G, Verhoef, Senno, Rookus, Matti A, Pruntel, Roelof, van der Hout, Annemarie H, Hogervorst, Frans B L, Kluijt, I, Sijmons, Rolf H, Aalfs, Cora M, Wagner, Anja, Ausems, Margreet G E M, Hoogerbrugge, Nicoline, van Asperen, Christi J, Gomez Garcia, Encarna B, Meijers-Heijboer, Hanne, ten Kate, Leo P, Menko, Fred H, van 't Veer, Laura J
Published in Journal of medical genetics (01.06.2010)
Published in Journal of medical genetics (01.06.2010)
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Concordance for pre‐eclampsia in monozygous twins
Lachmeijer, A. M. A., Aarnoudse, J. G., Kate, L. P., Pals, G., Dekker, G. A.
Published in BJOG : an international journal of obstetrics and gynaecology (01.12.1998)
Published in BJOG : an international journal of obstetrics and gynaecology (01.12.1998)
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Costs, effects, and savings of screening for cystic fibrosis gene carriers
Wildhagen, M F, Hilderink, H B, Verzijl, J G, Verheij, J B, Kooij, L, Tijmstra, T, ten Kate, L P, Habbema, J D
Published in Journal of epidemiology and community health (1979) (01.07.1998)
Published in Journal of epidemiology and community health (1979) (01.07.1998)
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Participation in preconceptional carrier couple screening: characteristics, attitudes, and knowledge of both partners
Henneman, L, Bramsen, I, van der Ploeg, H M, Adèr, H J, van der Horst, H E, Gille, J J P, ten Kate, L P
Published in Journal of medical genetics (01.10.2001)
Published in Journal of medical genetics (01.10.2001)
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The nonhospital costs of care of patients with CF in The Netherlands: results of a questionnaire
Wildhagen, MF, Verheij, JB, Verzijl, JG, Gerritsen, J, Bakker, W, Hilderink, HB, ten Kate, LP, Tijmstra, T, Kooij, L, Habbema, JD
Published in The European respiratory journal (01.11.1996)
Published in The European respiratory journal (01.11.1996)
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Possibilities and barriers in the implementation of a preconceptional screening programme for cystic fibrosis carriers: a focus group study
Poppelaars, F.A.M, van der Wal, G, Braspenning, J.C.C, Cornel, M.C, Henneman, L, Langendam, M.W, ten Kate, L.P
Published in Public health (London) (01.11.2003)
Published in Public health (London) (01.11.2003)
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Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members
Bleiker, E.M.A, Aaronson, N.K, Menko, F.H, Hahn, D.E.E, van Asperen, C.J, Rutgers, E.J.T, ten Kate, L.P, Leschot, N.J
Published in Patient education and counseling (01.09.1997)
Published in Patient education and counseling (01.09.1997)
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Cost of care of patients with cystic fibrosis in The Netherlands in 1990-1
Wildhagen, M F, Verheij, J B, Verzijl, J G, Hilderink, H B, Kooij, L, Tijmstra, T, ten Kate, L P, Gerritsen, J, Bakker, W, Habbema, J D, Habbema, F
Published in Thorax (01.03.1996)
Published in Thorax (01.03.1996)
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Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
Kelmemi, W, Teeuw, M E, Bochdanovits, Z, Ouburg, S, Jonker, M A, Alkuraya, F, Hashem, M, Kayserili, H, van Haeringen, A, Sheridan, E, Masri, A, Cobben, J M, Rizzu, P, Kostense, P J, Dommering, C J, Henneman, L, Bouhamed-Chaabouni, H, Heutink, P, Ten Kate, L P, Cornel, M C
Published in BMC medical genetics (20.07.2015)
Published in BMC medical genetics (20.07.2015)
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Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease
Cobben, Jan M., Breuning, Martijn H., Schoots, Coen, ten Kate, Leo P., Zerres, Klaus
Published in Kidney international (01.11.1990)
Published in Kidney international (01.11.1990)
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Number and sex of offspring of delta F508 carriers outside cystic fibrosis families
de Vries, H G, Collée, J M, Meeuwsen, W P, Scheffer, H, Ten Kate, L P
Published in Human genetics (01.05.1995)
Published in Human genetics (01.05.1995)
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DOWN SYNDROME IN THE FAMILY: WHAT TO DO WHEN THE KARYOTYPE OF THE PROBAND IS NOT AVAILABLE
TUERLINGS, J. H. A. M., OOSTERWIJK, J. C., TEN KATE, L. P.
Published in Prenatal diagnosis (01.06.1996)
Published in Prenatal diagnosis (01.06.1996)
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A boy with Poland anomaly and facio-auriculo-vertebral dysplasia
Cobben, J M, van Essen, A J, McParland, P C, Polman, H A, ten Kate, L P
Published in Clinical genetics (01.02.1992)
Published in Clinical genetics (01.02.1992)
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