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Genomics|January 27, 1998
Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11B Funke, B Saint-Jore, A Puech, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Genomics|November 15, 1994
Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129S A Carter, S D Bryce, C S Munro, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 1998
Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organizationA Puech, B Saint-Jore, B Funke, et al.
The Journal of Biological Chemistry|March 23, 2001
Functional characterization of transforming growth factor beta signaling in Smad2- and Smad3-deficient fibroblastsE Piek, W J Ju, J Heyer, et al.
Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.
Genomics|April 1, 1997
Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndromeH Sirotkin, H O'Donnell, R DasGupta, et al.
Cell|May 6, 1998
Somatic inactivation of Pkd2 results in polycystic kidney diseaseG Wu, V D'Agati, Y Cai, et al.
Cell|June 28, 1996
Meiotic pachytene arrest in MLH1-deficient miceW Edelmann, P E Cohen, M Kane, et al.
Carcinogenesis|February 1, 1997
Loss of Apc and the entire chromosome 18 but absence of mutations at the Ras and Tp53 genes in intestinal tumors from Apc1638N, a mouse model for Apc-driven carcinogenesisR Smits, A Kartheuser, S Jagmohan-Changur, et al.
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