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Human Mutation|June 28, 2007
Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndromeJan D Marshall, Elizabeth G Hinman, Gayle B Collin, et al.Human Mutation|July 25, 2007
Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemiaRadek Cmejla, Jana Cmejlova, Helena Handrkova, et al.Human Mutation|July 11, 2007
Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridizationYao-Shan Fan, Parul Jayakar, Hongbo Zhu, et al.Human Mutation|July 12, 2007
Genetic variant in the HSPB1 promoter region impairs the HSP27 stress responseInes Dierick, Joy Irobi, Sophie Janssens, et al.Human Mutation|July 31, 2007
Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrioJason C Ting, Elisha D O Roberson, Nathaniel D Miller, et al.Human Mutation|July 28, 2007
The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutationsPaolo Comeglio, Philip Johnson, Gavin Arno, et al.Human Mutation|May 12, 2007
Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic DatabaseJoël Zlotogora, Sjozef van Baal, George P PatrinosHuman Mutation|June 5, 2007
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genesGuy Froyen, Hilde Van Esch, Marijke Bauters, et al.Human Mutation|June 5, 2007
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearingNevra Nal, Zubair M Ahmed, Engin Erkal, et al.Human Mutation|April 28, 2007
Type 1 Gaucher disease: null and hypomorphic novel chitotriosidase mutations-implications for diagnosis and therapeutic monitoringMarie E Grace, Manisha Balwani, Irina Nazarenko, et al.Pageof 575