I. Mulder

发表

Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.

S. Castedo, G. Tan-Sindhunata, B. Leegte, 2000, American journal of medical genetics.

Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy

R. Hofstra, J. T. Dunnen, A. Essen, 2003, American journal of medical genetics. Part A.

Improvement of fragment and primer selection for mutation detection by denaturing gradient gel electrophoresis.

J. Osinga, R. Hofstra, R. Hofstra, 1998, Nucleic acids research.

Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations

R. Eeles, J. Wesseling, J. Oosterwijk, 2005, Journal of Medical Genetics.

DGGE‐based whole‐gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients

R. Vossen, R. Hofstra, J. D. den Dunnen, 2004, Human mutation.

A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting

H. Meijers-Heijboer, S. Verhoef, R. Hofstra, 2006, Human mutation.

Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene

R. Hofstra, E. Friedman, M. Buchfelder, 2000 .

Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non‐Ashkenazi Jewish women with familial breast and ovarian cancer

P. Oefner, M. Papa, R. Hofstra, 2000, Human mutation.

Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresis.

J. Osinga, R. Hofstra, R. Hofstra, 1999, Nucleic acids research.