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Human Molecular Genetics|August 1, 1995
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneityL Parmentier, C Blanchet-Bardon, S Nguyen, et al.
Human Genetics|April 1, 1998
Linkage between atopy and the IgE high-affinity receptor gene at 11q13 in atopic dermatitis familiesR Fölster-Holst, H W Moises, L Yang, et al.
American Journal of Human Genetics|January 1, 1995
Refining the localization of the PKD2 locus on chromosome 4q by linkage analysis in Spanish families with autosomal dominant polycystic kidney disease type 2J L San Millán, M Viribay, B Peral, et al.
Gene|July 13, 2004
Global heterochromatic colocalization of transposable elements with minisatellites in the compact genome of the pufferfish Tetraodon nigroviridisCécile Fischer, Laurence Bouneau, Jean-Pierre Coutanceau, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
A 10-cM YAC contig spanning GLC1A, the primary open-angle glaucoma locus at 1q23-q25C Clépet, H J Dauwerse, C Desmaze, et al.
American Journal of Human Genetics|October 1, 1995
Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15J Schleutker, P Leppänen, J E Månsson, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 14, 1998
Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNAF Salomon-Nguyen, M Le Coniat-Busson, R Heilig, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1996
Regional assignment of human ESTs by whole-genome radiation hybrid mappingP D Hayes, K Schmitt, H B Jones, et al.
The EMBO Journal|July 1, 1985
Extensive DNA sequence homologies between the human Y and the long arm of the X chromosomeD Geldwerth, C Bishop, G Guellaën, et al.
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