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Annals of Neurology|October 23, 1997
The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigreesS Claes, K Devriendt, L Lagae, et al.Human Molecular Genetics|May 1, 1993
X-linked liver glycogenosis: localization and isolation of a candidate geneJ Hendrickx, P Coucke, P Bossuyt, et al.American Journal of Medical Genetics|December 15, 1994
Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excludedA De bruyn, P Raeymaekers, K Mendelbaum, et al.Human Molecular Genetics|August 1, 1996
Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian familyT Fagerheim, O Nilssen, P Raeymaekers, et al.Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.American Journal of Human Genetics|August 1, 1992
Further localization of X-linked hydrocephalus in the chromosomal region Xq28P J Willems, L Vits, P Raeymaekers, et al.Neurology|June 1, 1989
Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markersP Raeymaekers, P De Jonghe, H Backhovens, et al.American Journal of Human Genetics|October 1, 1990
Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12V Timmerman, P Raeymaekers, P De Jonghe, et al.Journal of Medical Genetics|March 2, 1999
Homozygosity mapping to the USH2A locus in two isolated populationsT Fagerheim, P Raeymaekers, J Merren, et al.American Journal of Human Genetics|December 1, 1989
Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I)P Raeymaekers, V Timmerman, P De Jonghe, et al.Pageof 5