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Identification of C12orf4 as a gene for autosomal recessive intellectual disability
by
Philips, A.K.
,
Pinelli, M.
,
de Bie, C.I.
,
Mustonen, A.
,
Määttä, T.
,
Arts, H.H.
,
Wu, K.
,
Roepman, R.
,
Moilanen, J.S.
,
Raza, S.
,
Varilo, T.
,
Scala, G.
,
Cocozza, S.
,
Gilissen, C.
,
van Gassen, K.L.I.
,
Järvelä, I.
Published in
Clinical genetics
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Interaction of Nephrocystin-4 and RPGRIP1 Is Disrupted by Nephronophthisis or Leber Congenital Amaurosis-Associated Mutations
by
Ronald Roepman
,
Stef J. F. Letteboer
,
Heleen H. Arts
,
Sylvia E. C. van Beersum
,
Xinrong Lu
,
Krieger, Elmar
,
Ferreira, Paulo A.
,
Frans P. M. Cremers
,
Nathans, Jeremy
Published in
Proceedings of the National Academy of Sciences - PNAS
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Alteration of nephrocystins and IFT-A proteins causes similar ciliary phenotypes leading to Nephronophthisis
by
Saunier, S
,
Bizet, AA
,
Silbermann, F
,
Filhol, E
,
Blisnick, T
,
Henneveu, A
,
Montenont, E
,
Perrault, I
,
Boyle-Feysot, C
,
Rozet, J-M
,
Bastin, P
,
Arts, HH
,
Antignac, C
,
Benmerah, AR
Published in
Cilia (London)
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Heat‐shock‐protein‐27(HSP27) expression in ovarian carcinoma: Relation in response to chemotherapy and prognosis
by
Arts, Henriette J.G.
,
Hollema, Harry
,
Lemstra, Willy
,
Willemse, Pax H.B.
,
De Vries, Elisabeth G.E.
,
Kampinga, Harm H.
,
Van der Zee, Ate G.J.
Published in
International journal of cancer
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Age-related response to lidocaine-prilocaine (EMLA) emulsion and effect of music distraction on the pain of intravenous cannulation
by
ARTS, S. E
,
ABU-SAAD, H. H
,
CHAMPION, G. D
,
CRAWFORD, M. R
,
FISHER, R. J
,
JUNIPER, K. H
,
ZIEGLER, J. B
Published in
Pediatrics (Evanston)
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An Analysis of Human Response to the Irritancy of Acetone Vapors
by
Arts, J.H.E.
,
Mojet, J.
,
Gemert, L.J. van
,
Emmen, H.H.
,
Lammers, J.H.C.M.
,
Marquart, J.
,
Woutersen, R.A.
,
Feron, V.J.
Published in
Critical reviews in toxicology
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Quality of working life and workload in home help services: A review of the literature a proposal for a research model
by
Arts, Suzanne E.J.
,
Kerkstra, Ada
,
van der Zee, Jouke
,
Abu‐Saad, Huda Huyer
Published in
Scandinavian journal of caring sciences
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Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood
by
KREMER, H
,
HAMEL, B. C. J
,
VAN DEN HELM, B
,
ARTS, W. F. M
,
DE WIJS, I. J
,
SISTERMANS, E. A
,
ROPERS, H.-H
,
MARIMAN, E. C. M
Published in
Human genetics
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