CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype von Bergman, J E H, Janssen, N, Hoefsloot, L H, Jongmans, M C J, Hofstra, R M W, van Ravenswaaij-Arts, C M A

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Health risks for ataxia-telangiectasia mutated heterozygotes: a systematic review, meta-analysis and evidence-based guideline von van Os, N.J.H., Roeleveld, N., Weemaes, C.M.R., Jongmans, M.C.J., Janssens, G.O., Taylor, A.M.R., Hoogerbrugge, N., Willemsen, M.A.A.P.

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Renal cell carcinoma in young FH mutation carriers: case series and review of the literature von Hol, J. A., Jongmans, M. C. J., Littooij, A. S., de Krijger, R. R., Kuiper, R. P., van Harssel, J. J. T., Mensenkamp, A., Simons, M., Tytgat, G. A. M., van den Heuvel-Eibrink, M. M., van Grotel, M.

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A novel germline PAX5 single exon deletion in a pediatric patient with precursor B-cell leukemia von van Engelen, N., Roest, M., van Dijk, F., Sonneveld, E., Bladergroen, R., van Reijmersdal, S. V., van der Velden, V. H. J., Hoogeveen, P. G., Kors, W. A., Waanders, E., Jongmans, M. C. J., Kuiper, R. P.

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What influences participation in leisure activities of children and youth with physical disabilities? A systematic review von Bult, M.K., Verschuren, O., Jongmans, M.J., Lindeman, E., Ketelaar, M.

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A home-video method to assess infant gross motor development: parent perspectives on feasibility von Boonzaaijer, M, van Wesel, F, Nuysink, J, Volman, M J M, Jongmans, M J

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Germline activating TYK2 mutations in pediatric patients with two primary acute lymphoblastic leukemia occurrences von Waanders, E, Scheijen, B, Jongmans, M C J, Venselaar, H, van Reijmersdal, S V, van Dijk, A H A, Pastorczak, A, Weren, R D A, van der Schoot, C E, van de Vorst, M, Sonneveld, E, Hoogerbrugge, N, van der Velden, V H J, Gruhn, B, Hoogerbrugge, P M, van Dongen, J J M, Geurts van Kessel, A, van Leeuwen, F N, Kuiper, R P

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The AIMS home-video method: parental experiences and appraisal for use in neonatal follow-up clinics von Suir, I, Oosterhaven, J, Boonzaaijer, M, Nuysink, J, Jongmans, M

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Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma von van Engelen, N., van Dijk, F., Waanders, E., Buijs, A., Vermeulen, M. A., Loeffen, J. L. C., Kuiper, R. P., Jongmans, M. C. J.

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Childhood neuroendocrine tumours: a descriptive study revealing clues for genetic predisposition von Diets, I J, Nagtegaal, I D, Loeffen, J, de Blaauw, I, Waanders, E, Hoogerbrugge, N, Jongmans, M C J

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Parents' experiences with sequencing of all known pediatric cancer predisposition genes in children with cancer von Bon, S.B.B., Wouters, R.H.P., Bakhuizen, J.J., van den Heuvel-Eibrink, M.M., Maurice-Stam, H., Jongmans, M.C.J., Grootenhuis, M.A.

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Information seeking by parents of children with physical disabilities: An exploratory qualitative study von Alsem, M.W., Ausems, F., Verhoef, M., Jongmans, M.J., Meily-Visser, J.M.A., Ketelaar, M.

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CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene von Jongmans, M C J, Admiraal, R J, van der Donk, K P, Vissers, L E L M, Baas, A F, Kapusta, L, van Hagen, J M, Donnai, D, de Ravel, T J, Veltman, J A, Geurts van Kessel, A, De Vries, B B A, Brunner, H G, Hoefsloot, L H, van Ravenswaaij, C M A

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Long-term outcome after neonatal hypoxic-ischaemic encephalopathy von de Vries, Linda S, Jongmans, Marian J

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Independent development of lymphoid and histiocytic malignancies from a shared early precursor von Waanders, E, Hebeda, K M, Kamping, E J, Groenen, P J T A, Simons, A, Hoischen, A, Jongmans, M C J, Hoogerbrugge, P M, van Leeuwen, F N, Kuiper, R P, te Loo, D M W M

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CHD7 mutations in patients initially diagnosed with Kallmann syndrome - the clinical overlap with CHARGE syndrome von Jongmans, MCJ, Van Ravenswaaij-Arts, CMA, Pitteloud, N, Ogata, T, Sato, N, Claahsen-van der Grinten, HL, Van Der Donk, K, Seminara, S, Bergman, JEH, Brunner, HG, Crowley Jr, WF, Hoefsloot, LH

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Modeling gross motor developmental curves of extremely and very preterm infants using the AIMS home-video method von Suir, I, Boonzaaijer, M, Oudgenoeg-Paz, O, Westers, P, de Vries, L S, van der Net, J, Nuysink, J, Jongmans, M J

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Effectiveness of a computerised working memory training in adolescents with mild to borderline intellectual disabilities von Van der Molen, M. J., Van Luit, J. E. H., Van der Molen, M. W., Klugkist, I., Jongmans, M. J.

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Early gross motor development of preterm infants according to the Alberta Infant Motor Scale von van Haastert, I.C., de Vries, L.S., Helders, P.J.M., Jongmans, M.J.

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Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome von Jongmans, M C J, Kuiper, R P, Carmichael, C L, Wilkins, E J, Dors, N, Carmagnac, A, Schouten-van Meeteren, A Y N, Li, X, Stankovic, M, Kamping, E, Bengtsson, H, Schoenmakers, E F P M, van Kessel, A Geurts, Hoogerbrugge, P M, Hahn, C N, Brons, P P, Scott, H S, Hoogerbrugge, N

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