No mutation in the gene for Noonan syndrome, <i>PTPN11</i>, in 18 patients with Costello syndrome
Birte Tröger(Universität Hamburg), Peter Meinecke(University Medical Center Groningen), Elke Hobbiebrunken(University of Göttingen), Zsuzsanna Almássy(Boston Children's Hospital), Hanno J. Bolz(BioScientia (Poland)), Peter Freisinger(TUM Klinikum), Andreas Gal(Universität Hamburg), Dagmar Wieczorek(Essen University Hospital), M Stefanova(Medical University Plovdiv), Kerstin Kutsche(Universität Hamburg), Berthold Streubel(Medical University of Vienna), Michel Morlot(Kinderkrankenhaus auf der Bult), Sabine Lüttgen(Universität Hamburg), Almuth Caliebe(Christian-Albrechts-Universität zu Kiel)
Cited by 19
Related Papers
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis
|Nature|2006|661
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder
|The American Journal of Human Genetics|2008|581
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
|Nature Genetics|2010|509
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
|Nature Genetics|2001|497