RePub, Erasmus University Repository

A G→A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2 Article

Human Molecular Genetics, 7(3), 393-398.

J.E.M.M. de Klein (Annelies), P.H.J. Riegman (Peter), E.K. Bijlsma (Emilia), A. Heldoorn (Anneliek), M. Muijtjens (Manja), M.A. den Bakker (Michael), C.J.J. Avezaat (Cees) and E.C. Zwarthoff (Ellen)

March 1998
Standard properties of ultrasound contrast agents Article

Ultrasound in Medicine & Biology, 24(3), 469-472.

A. Bouakaz (Ayache), N. de Jong (Nico) and C. Cachard (Christian)

March 1998
Perceived parental attitude, alexithymia and defense style in psychiatric outpatients Article

Psychotherapy and Psychosomatics, 67(2), 81-87.

C.G. Kooiman (Cornelis), P. Spinhoven (Ph), R.W. Trijsburg (Wim) and H.G.M. Rooijmans (Harry G.)

March 1998
An estimate of fetal autonomic state by spectral analysis of human umbilical artery flow velocity waveforms Article

Cardiovascular Research, 37(3), 601-605.

N.T.C. Ursem (Nicolette), H. Kempski (Helena), M.A.J. de Ridder (Maria), E.B. Clark and J.W. Wladimiroff (Juriy)

March 1998
Bibingka strategy to land reform and implementation : autonomous peasant mobilizations and state reformists in the Philippines Research Paper

ISS Working Papers - General Series

S.M. Borras jr. (Saturnino)

March 1998
Evaluation of a new maintenance concept for the preservation of highways Article

I M A Journal of Management Mathematics, 109-156.

R. Dekker (Rommert), R.P. Plasmeijer and J.H. Swart

March 1998
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency Conference Paper

E.G. van Grunsven (Elisabeth), E. van Berkel (Emanuel), L. Ijlst (L.), P. Vreken (P.), J.B.C. de Klerk (Johannes), J. Adamski (Jerzy), H. Lemonde (Hugh), P. Clayton (Peter), D.A. Cuebas (Dean) and R.J.A. Wanders (Ronald)

March 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy Article

Nature Genetics, 18(2), 164-167.

B. Brais (Bernard), J.-P. Bouchard (Jean-Pierre), Y.-G. Xie (Ya-Gang), D.L. Rochefort (Daniel), N. Chrétien (Nathalie), F.M.S. Tomé (Fernando), R.G. Lafrenière (Ronald), J.M. Rommens (Johanna), E. Uyama (Eichiro), O. Nohira (Osamu), et al. G.A. Rouleau

March 1998

Publication

A G→A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2 Article

Standard properties of ultrasound contrast agents Article

Perceived parental attitude, alexithymia and defense style in psychiatric outpatients Article

An estimate of fetal autonomic state by spectral analysis of human umbilical artery flow velocity waveforms Article

Bibingka strategy to land reform and implementation : autonomous peasant mobilizations and state reformists in the Philippines Research Paper

Evaluation of a new maintenance concept for the preservation of highways Article

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency Conference Paper

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy Article

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Publication

A G→A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2 Article

Standard properties of ultrasound contrast agents Article

Perceived parental attitude, alexithymia and defense style in psychiatric outpatients Article

An estimate of fetal autonomic state by spectral analysis of human umbilical artery flow velocity waveforms Article

Bibingka strategy to land reform and implementation : autonomous peasant mobilizations and state reformists in the Philippines Research Paper

Evaluation of a new maintenance concept for the preservation of highways Article

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency Conference Paper

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy Article

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