Ingrid Mbh van de Laar

Summary

Affiliation: Erasmus MC
Country: The Netherlands

Publications

  1. ncbi request reprint Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype
    Ingrid Van de Laar
    Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands
    Am J Med Genet A 143:2712-5. 2007
  2. doi request reprint Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome
    Ingrid M B H van de Laar
    Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands
    J Med Genet 49:47-57. 2012
  3. pmc Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities
    Malgorzata I Srebniak
    Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands
    Mol Cytogenet 5:14. 2012

Collaborators

Detail Information

Publications3

  1. ncbi request reprint Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype
    Ingrid Van de Laar
    Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands
    Am J Med Genet A 143:2712-5. 2007
    ..The present observations provide further support to this hypothesis...
  2. doi request reprint Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome
    Ingrid M B H van de Laar
    Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands
    J Med Genet 49:47-57. 2012
    ..AOS is caused by mutations in the SMAD3 gene...
  3. pmc Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities
    Malgorzata I Srebniak
    Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands
    Mol Cytogenet 5:14. 2012
    ....