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Human Molecular Genetics|February 1, 1994
Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complexA F Roux, J Rommens, C McDowell, et al.Human Molecular Genetics|February 1, 1994
An explanation for the constitutive exon 9 cassette splicing of the DMD geneJ Reiss, F RininslandHuman Molecular Genetics|September 1, 1993
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VIIO Takamiya, G Kemball-Cook, D M Martin, et al.Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.Human Molecular Genetics|September 1, 1993
Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcriptsJ Gecz, L Villard, A M Lossi, et al.Human Molecular Genetics|September 1, 1993
Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophyM Anvret, G Ahlberg, U Grandell, et al.Human Molecular Genetics|October 28, 2005
A segment of the Mecp2 promoter is sufficient to drive expression in neuronsMegumi Adachi, Edward W Keefer, Frederick S JonesHuman Molecular Genetics|November 19, 2005
Molecular complementation of IL-12Rbeta1 deficiency reveals functional differences between IL-12Rbeta1 alleles including partial IL-12Rbeta1 deficiencyEsther van de Vosse, Roelof A de Paus, Jaap T van Dissel, et al.Human Molecular Genetics|October 26, 2005
Genetical genomics: combining genetics with gene expression analysisJun Li, Margit BurmeisterHuman Molecular Genetics|October 26, 2005
Camels and zebrafish, viruses and cancer: a microRNA updateEugene Berezikov, Ronald H A PlasterkPageof 1,196