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Human Genetics|November 1, 1993
Molecular analysis of mutations in the gene FMR-1 segregating in fragile X familiesP Steinbach, D Wöhrle, G Tariverdian, et al.
Cytogenetic and Genome Research|February 7, 2008
Specific transcriptional changes in human fetuses with autosomal trisomiesO Altug-Teber, M Bonin, M Walter, et al.
Genomics|January 25, 2000
A novel ribosomal S6-kinase (RSK4; RPS6KA6) is commonly deleted in patients with complex X-linked mental retardationH G Yntema, B van den Helm, J Kissing, et al.
Human Molecular Genetics|September 1, 1996
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4Y J de Kok, E R Vossenaar, C W Cremers, et al.
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