Publications by authors named "Inge M Mulder"

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A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
Annemarie H van der Hout, Ans M W van den Ouweland, Rob B van der Luijt, Hans J P Gille, Daniëlle Bodmer, Inge M Mulder

Hum Mutat· July 2006

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DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
Robert M W Hofstra, Inge M Mulder, Rolf Vossen, Pia A M de Koning-Gans, Marian Kraak

Hum Mutat· January 2004

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Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy.
Anthonie J van Essen, Inge M Mulder, Pieter van der Vlies, Annemarie H van der Hout, Charles H C M Buys

Am J Med Genet A· April 2003

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