Bex1 , a gene with increased expression in parthenogenetic embryos, is a member of a novel gene family on the mouse X chromosome

By Brown A.L.   Kay G.F.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 611-619

Oxford University Press

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A radiation hybrid map of the region in pigs demonstrates conserved gene order compared with the human and mouse genomes

By Robic Annie   Seroude Virginie   Jeon Jin-Tae   Yerle Martine   Wasungu Luc   Andersson Leif   Gellin Joël   Milan Denis  

Mammalian Genome, Vol. 10, Iss. 6, 1999-06 ,pp. : 565-568

Springer Publishing Company

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A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

By Koide Reiji   Kobayashi Shigeichi  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2047-2053

Oxford University Press

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A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse

By Semina E.V.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 415-422

Oxford University Press

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A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation

By Harzer K.  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 927-940

Oxford University Press

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