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Results:
1-8
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Results: 8
Authors:
Sijmons, RH
Boonstra, AE
Reefhuis, J
Hordijk-Hos, JM
de Walle, HEK
Oosterwijk, JC
Cornel, MC
Citation: Rh. Sijmons et al., Accuracy of family history of cancer: clinical genetic implications, EUR J HUM G, 8(3), 2000, pp. 181-186
Authors:
Hoogerwaard, EM
van der Wouw, PA
Wilde, AAM
Bakker, E
Ippel, PF
Oosterwijk, JC
Majoor-Krakauer, DF
van Essen, AJ
Leschot, NJ
de Visser, M
Citation: Em. Hoogerwaard et al., Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy, NEUROMUSC D, 9(5), 1999, pp. 347-351
Authors:
Oosterwijk, JC
Citation: Jc. Oosterwijk, Genetic aspects of (gynecological) tumours, EUR J OB GY, 82(2), 1999, pp. 125-128
Authors:
Oosterwijk, JC
Citation: Jc. Oosterwijk, Prenatal diagnosis on fetal cells from maternal blood: approaches and perspectives, EUR J OB GY, 82(2), 1999, pp. 169-170
Authors:
de Bock, GH
Vlieland, TPMV
Hageman, GCHA
Oosterwijk, JC
Springer, MP
Kievit, J
Citation: Gh. De Bock et al., The assessment of genetic risk of breast cancer: a set of GP guidelines, FAM PRACT, 16(1), 1999, pp. 71-77
Authors:
Berends, MJW
Hordijk, R
Scheffer, H
Oosterwijk, JC
Halley, DJJ
Sorgedrager, N
Citation: Mjw. Berends et al., Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype, AM J MED G, 84(1), 1999, pp. 76-79
Authors:
Hoogerwaard, EM
Bakker, E
Ippel, PF
Oosterwijk, JC
Majoor-Krakauer, DF
Leschot, NJ
Van Essen, AJ
Brunner, HG
van der Wouw, PA
Wilde, AAM
de Visser, M
Citation: Em. Hoogerwaard et al., Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study, LANCET, 353(9170), 1999, pp. 2116-2119
Authors:
Oosterwijk, JC
Knepfle, CFHM
Mesker, WE
Vrolijk, H
Sloos, WCR
Pattenier, H
Ravkin, I
van Ommen, GJB
Kanhai, HHH
Tanke, HJ
Citation: Jc. Oosterwijk et al., Strategies for rare-event detection: An approach for automated fetal cell detection in maternal blood, AM J HU GEN, 63(6), 1998, pp. 1783-1792
Risultati:
1-8
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