Author/Creator: Schrander-Stumpel, C T - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Schrander-Stumpel, C T

1. Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis. Issue 1 (January 1993)

Authors:: Schrander-Stumpel, C T; Höweler, C J; Reekers, A D; De Smet, N M; Hall, J G; Fryns, J P
Journal:: Journal of medical genetics
Issue:: Volume 30:Issue 1(1993)
Page Start:: 78
Record Type:: Journal Article
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2. Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family. Issue 10 (October 1998)

Authors:: Verhoef, S; Schrander-Stumpel, C T; Vuzevski, V D; Tempelaars, A; Jansen, L A; Malfeyt, G A; Ceelen, T L; Lindhout, D; Halley, D J; van den Ouweland, A M
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 10(1998)
Page Start:: 841
Record Type:: Journal Article
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3. Oculoauriculovertebral spectrum and cerebral anomalies. Issue 5 (May 1992)

Authors:: Schrander-Stumpel, C T; de Die-Smulders, C E; Hennekam, R C; Fryns, J P; Bouckaert, P X; Brouwer, O F; da Costa, J J; Lommen, E J; Maaswinkel-Mooy, P D
Journal:: Journal of medical genetics
Issue:: Volume 29:Issue 5(1992)
Page Start:: 326
Record Type:: Journal Article
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4. PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida. Issue 8 (August 1996)

Authors:: Hol, F A; Geurds, M P; Chatkupt, S; Shugart, Y Y; Balling, R; Schrander-Stumpel, C T; Johnson, W G; Hamel, B C; Mariman, E C
Journal:: Journal of medical genetics
Issue:: Volume 33:Issue 8(1996)
Page Start:: 655
Record Type:: Journal Article
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