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Results:
1-12
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Results: 12
Authors:
de Vries, BBA
van't Hoff, WG
Surtees, RAH
Winter, RM
Citation: Bba. De Vries et al., Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay, CLIN DYSMOR, 10(2), 2001, pp. 115-121
Authors:
de Vries, BBA
Lees, M
Knight, SJL
Regan, R
Corney, D
Flint, J
Barnicoat, A
Winter, RM
Citation: Bba. De Vries et al., Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13), AM J MED G, 99(4), 2001, pp. 314-319
Authors:
de Vries, BBA
White, SM
Knight, SJL
Regan, R
Homfray, T
Young, ID
Super, M
McKeown, C
Splitt, M
Quarrell, OWJ
Trainer, AH
Niermeijer, MF
Malcolm, S
Flint, J
Hurst, JA
Winter, RM
Citation: Bba. De Vries et al., Clinical studies on submicroscopic subtelomeric rearrangements: a checklist, J MED GENET, 38(3), 2001, pp. 145-150
Authors:
de Vries, BBA
Oostra, BA
Citation: Bba. De Vries et Ba. Oostra, The fragile X syndrome: A model for mental retardation, NEUROSC R C, 26(3), 2000, pp. 255-263
Authors:
de Vries, BBA
Bitner-Glindzicz, M
Knight, SJL
Tyson, J
MacDermot, KD
Flint, J
Malcolm, S
Winter, RM
Citation: Bba. De Vries et al., A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome, CLIN GENET, 58(6), 2000, pp. 483-487
Authors:
de Vries, BBA
Arts, WFM
Breedveld, GJ
Hoogeboom, JJM
Niermeijer, MF
Heutink, P
Citation: Bba. De Vries et al., Benign hereditary chorea of early onset maps to chromosome 14q, AM J HU GEN, 66(1), 2000, pp. 136-142
Authors:
de Vries, BBA
Kleijer, WJ
Keulemans, JLM
Voznyi, YV
Franken, PF
Eurlings, MCM
Galjaard, RJ
Losekoot, M
Catsman-Berrevoets, CE
Breuning, MH
Taschner, PEM
van Diggelen, OP
Citation: Bba. De Vries et al., First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysis, PRENAT DIAG, 19(6), 1999, pp. 559-562
Authors:
de Vries, BBA
Eussen, BHJ
van Diggelen, OP
van der Heide, A
Deelen, WH
Govaerts, LCP
Lindhout, D
Wouters, CH
Van Hemel, JO
Citation: Bba. De Vries et al., Submicroscopic xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14), AM J MED G, 87(2), 1999, pp. 189-194
Authors:
de Vries, BBA
Mohkamsing, S
van den Ouweland, AMW
Mol, E
Gelsema, K
van Rijn, M
Tibben, A
Halley, DJJ
Duivenvoorden, HJ
Oostra, BA
Niermeijer, MF
Citation: Bba. De Vries et al., Screening for the fragile X syndrome among the mentally retarded: a clinical study, J MED GENET, 36(6), 1999, pp. 467-470
Authors:
de Vries, BBA
van den Boer-van den Berg, HMA
Niermeijer, MF
Tibben, A
Citation: Bba. De Vries et al., Dilemmas in Counselling females with the fragile X syndrome, J MED GENET, 36(2), 1999, pp. 167-170
Authors:
Willemsen, R
Anar, B
Otero, YD
de Vries, BBA
Hilhorst-Hofstee, Y
Smits, A
van Looveren, E
Willems, PJ
Galjaard, H
Oostra, BA
Citation: R. Willemsen et al., Noninvasive test for fragile X syndrome, using hair root analysis, AM J HU GEN, 65(1), 1999, pp. 98-103
Authors:
de Vries, BBA
Mohkamsing, S
van den Ouweland, AMW
Halley, DJJ
Niermeijer, MF
Oostra, BA
Willemsen, R
Citation: Bba. De Vries et al., Screening with the FMR1 protein test among mentally retarded males, HUM GENET, 103(4), 1998, pp. 520-522
Risultati:
1-12
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