Publications by authors named "Ingegerd Fransson"

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Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
Myriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, Tiffany L Smith, Martine Dunnwald, Ingegerd Fransson

Am J Hum Genet· January 2014

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Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients.
Sara Bruce, Katariina Hannula-Jouppi, Mari Puoskari, Ingegerd Fransson, Kalle O J Simola

J Med Genet· December 2010

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Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.
Elina Salmela, Tuuli Lappalainen, Ingegerd Fransson, Peter M Andersen, Karin Dahlman-Wright

PLoS One· January 2009

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Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
Hong Jiao, Beáta Tóth, Melinda Erdos, Ingegerd Fransson, Eva Rákóczi

Mol Immunol· November 2008

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Heidi Anthoni, Marco Zucchelli, Hans Matsson, Bertram Müller-Myhsok, Ingegerd Fransson

Hum Mol Genet· March 2007

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Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
Myriam Peyrard-Janvid, Marie Pegelow, Hannele Koillinen, Catharina Larsson, Ingegerd Fransson

Eur J Hum Genet· December 2005

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Strong conservation of the human NF2 locus based on sequence comparison in five species.
Caisa M Hansson, Haider Ali, Carl E G Bruder, Ingegerd Fransson, Sindy Kluge

Mamm Genome· August 2003

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A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
Patrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, Isabel Tapia-Páez, Teresita Diaz De Ståhl, Ingegerd Fransson

Hum Mol Genet· December 2002

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