J. van de Kamp

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A large retinoblastoma detected in a fetus at 21 weeks of gestation

D. Oepkes, C. Vermeij-Keers, J. J. van de Kamp, 1993, Prenatal diagnosis.

Etiology and recurrence risk in Rubinstein-Taybi syndrome.

R. Hennekam, C. Stevens, R. Hennekam, 2005, American journal of medical genetics. Supplement.

[Presymptomatic DNA diagnosis in Huntington's chorea: reactions to the certainty of not being a genetic carrier].

R. Roos, A. Tibben, F. Verhage, 1990, Nederlands tijdschrift voor geneeskunde.

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

J. C. Houwelingen, F. Rosendaal, G. V. Ommen, 1991, Journal of medical genetics.

Genotype Assignment of Haemophilia A by Use of Intragenic and Extragenic Restriction Fragment Length Polymorphisms

P. Pearson, J. Dreesen, R. Quadt, 1987, Thrombosis and Haemostasis.

lntragenic Restriction-Fragment Length Polymorphism

P. Pearson, R. Bertina, R. Quadt, 2018 .

Intermittent thrombocytopenia and absent radii: report of a patient with additional unusual manifestations.

F. Veenstra, A. Haeringen, A. van Haeringen, 1989, American journal of medical genetics.

Erythrocyte superoxide dismutase deficiency in Fanconi's anaemia established by two independent methods of assay.

R. Frants, H. Joenje, F. Arwert, 1979, Scandinavian journal of clinical and laboratory investigation.

Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention.

R. Roos, H. Duivenvoorden, A. Tibben, 1993, American journal of medical genetics.

Monosomy 8p: an easily overlooked syndrome.

G. Beverstock, A. Bröcker-Vriends, F. van Bel, 1986, Journal of medical genetics.

Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature

P. Pearson, V. Bezrookove, G. Beverstock, 2003, American journal of medical genetics. Part A.

Follow-up on seven adult patients with mild Sanfilippo B-disease.

J. J. van de Kamp, H. M. van Schrojenstein-de Valk, J. van de Kamp, 1987, American journal of medical genetics.

Age at onset in Huntington's disease: effect of line of inheritance and patient's sex.

G. Bruyn, R. Roos, A. Moll, 1991, Journal of medical genetics.

Genetic counselling in hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) with nephropathy.

R. T. te Slaa, B. Hogewind, B. Looij, 1988, Journal of medical genetics.

First trimester prenatal diagnosis of haemophilia A: Two years' experience

P. Pearson, J. Dreesen, H. Kanhai, 1988, Prenatal diagnosis.

Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program.

R. Roos, A. Tibben, J. J. van de Kamp, 1994, American journal of human genetics.

On attitudes and appreciation 6 months after predictive DNA testing for Huntington disease in the Dutch program.

R. Roos, G. van Ommen, A. Tibben, 1993, American journal of medical genetics.

Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program.

G. van Ommen, H. Duivenvoorden, A. Tibben, 1993, American journal of medical genetics.

Detection of fetal erythroblasts in maternal blood by one-step gradient enrichment and immunocytochemical recognition.

H. Tanke, G. van Ommen, W. Mesker, 1996, Early human development.

Understanding the low uptake of presymptomatic DNA testing for Huntington's disease

G. Ommen, A. Tibben, F. Verhage, 1992, The Lancet.

Hypophosphatasia: biochemical screening of a Dutch kindred and evidence that urinary excretion of inorganic pyrophosphate is a marker for the disease.

J. Macfarlane, R. Russell, J. Macfarlane, 1988, Clinical chemistry.

Metacarpophalangeal pattern profile analysis in Rubinstein-Taybi syndrome.

R. Hennekam, P. Dijkstra, M. H. van den Boogaard, 2005, American journal of medical genetics. Supplement.