M. Donnér

发表

Chromosomal aberrations in a consecutive series of childhood rhabdomyosarcoma.

F. Mertens, N. Mandahl, C. Kullendorff, 1998, Medical and pediatric oncology.

Recurrent mutation Asn45 → Ser of glycoprotein IX in Bernard—Soulier syndrome

L. Holmberg, D. Karpman, A. Kristoffersson, 1996, European journal of haematology.

Type IIB von Willebrand's disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy.

I. Nilsson, L. Holmberg, M. Donnér, 1987 .

von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma.

E. Berntorp, I. Nilsson, L. Holmberg, 1986, Blood.

An Arg545→ Cys545 substitution mutation of the von Willebrand factor in type IIB von Willebrand's disease

B. Dahlbäck, I. Nilsson, L. Holmberg, 1991, European journal of haematology.

Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb

P. Nilsson, I. Dianzani, A. Haeringen, 1997, Nature Genetics.

Type IIB von Willebrand's disease: gene mutations and clinical presentation in nine families from Denmark, Germany and Sweden

H. Lenk, E. Scheibel, I. Nilsson, 1992, British journal of haematology.

Two new candidate mutations in type IIA von Willebrand's disease (ARG834→GLY, GLY846→ARG) and one polymorphism (TYR821→CYS) in the A2 region of the von Willebrand factor

B. Dahlbäck, E. Berntorp, E. Scheibel, 1993, European journal of haematology.

Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome.

M. Schwartz, L. Holmberg, K. Carlsson, 1988, Blood.

Clonal karyotypic evolution in a pediatric neurofibrosarcoma.

F. Mitelman, F. Mertens, N. Mandahl, 1995, Cancer genetics and cytogenetics.

Mutation Spectrum in Patients with Wiskott-Aldrich Syndrome and X-linked Thrombocytopenia: Identification of Twelve Different Mutations in the WASP Gene

M. Schwartz, L. Tranebjaerg, F. Skovby, 1996, Thrombosis and Haemostasis.

Cerebral infarction in a girl who developed anticardiolipin syndrome after acute lymphoblastic leukemia.

S. Garwicz, T. Wiebe, L. Holmberg, 1992, Pediatric hematology and oncology.

Recurrent chromosomal imbalances in choroid plexus tumors.

F. Mitelman, F. Mertens, N. Mandahl, 1995, Cancer genetics and cytogenetics.

An HphI‐polymorphism in exon 28 of the von Willebrand factor gene, and its frequency among patients with various forms of von Willebrand's disease

I. Nilsson, L. Holmberg, A. Kristoffersson, 1991, British journal of haematology.

IIB von W illebr and' s disease : mutations and clinical presentation in nine families Denmark, Germany and Sweden

B. Dahlbäck, H. Lenk, E. Scheibel, 1992 .

Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?

F. Mertens, N. Mandahl, T. Wiebe, 1999, Medical and pediatric oncology.

Platelet Surface‐bound IgG and Platelet‐specific IgG in Plasma in Childhood Thrombocytopenia

S. Garwicz, T. Wiebe, L. Holmberg, 1990, Acta paediatrica Scandinavica.

Childhood acute lymphoblastic leukaemia with ider(21)(q10)t(12;21)(p12;q22): a new recurrent abnormality showing ETV6/CBFA2 fusion

M. Höglund, B. Johansson, F. Mitelman, 1997, British journal of haematology.

Genetic polymorphism in a region of the vWF pseudogene corresponding to exon 28 of the vWF gene

B. Dahlbäck, L. Holmberg, A. Kristoffersson, 1992, European journal of haematology.