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Preview	Issue Date	Title	Author(s)
	1996	How many X-linked genes for non-specific mental retardation (MRX) are there?	Gedeon, A.; Donnelly, A.; Mulley, J.; Kerr, B.; Turner, G.
	1998	Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B	Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
	1995	X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome	Gedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J.
	1999	Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda	Gedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
	1999	Splice variants of the mouse Tec gene are differentially expressed in vivo	Merkel, A.; Atmosukarto, I.; Stevens, K.; Rathjen, P.; Booker, G.
	1997	Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics	Callen, D.; Yip, M.Y.; Eyre, H.
	1998	Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13.	Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
	1998	Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2y: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene.	Schollen, E.; Pardon, E.; Heykants, L.; Renard, J.P.; Doggett, N.; Callen, D.; Cassiman, J.J.; Matthijs, G.
	1999	Observations on the Variability of the H Reflex in Human Soleus	Funase, K.; Miles, T.
	1997	Characterization of the Capsular Polysaccharide Biosynthesis Locus of Streptococcus pneumoniae Type 19F	Paton, J.; Morona, J.; Morona, R.