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	Title	Authors / Editors	Date
unige:10963	Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse	Rajput, B.; Marshall, A.; Killary, A. M.; Lalley, P. A.; ... Strickland, S.	1987
unige:10920	The Y chromosome from autoimmune BXSB/MpJ mice induces a lupus-like syndrome in (NZW x C57BL/6)F1 male mice, but not in C57BL/6 male mice	Izui, Shozo; Higaki, M.; Morrow, D.; Merino, Ramon	1988
unige:11645	Igh-C allotype-linked control of anti-DNA production and clonotype expression in mice infected with Plasmodium yoelii	Yoshida, Haruyoshi; Fossati-Jimack, Liliane; Yoshida, M.; Abdelmoula, M.; ... Izui, Shozo	1988
unige:9127	Human chromosome 21: genome mapping and exploration, circa 1993	Antonarakis, Stylianos	1993
unige:11464	The Yaa gene abrogates the major histocompatibility complex association of murine lupus in (NZB x BXSB)F1 hybrid mice	Merino, Ramon; Iwamoto, Masahiro; Gershwin, M. E.; Izui, Shozo	1994
unige:8597	Genome linkage scanning: systematic or intelligent?	Antonarakis, Stylianos	1994
unige:9154	Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes	Chen, H.; Lowther, W.; Avramopoulos, D.; Antonarakis, Stylianos	1994
unige:8606	Schizophrenia susceptibility and chromosome 6p24-22	Antonarakis, Stylianos; Blouin, Jean-Louis; Pulver, A. E.; Wolyniec, P.; ... Dombroski, B.	1995
unige:8645	A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination	Blouin, Jean-Louis; Christie, D. H.; Gos, A.; Lynn, A.; ... Antonarakis, Stylianos	1995
unige:9130	Molecular etiology of factor VIII deficiency in hemophilia A	Antonarakis, Stylianos; Kazazian, H. H.; Gitschier, J.; Hutter, P.; ... Morris, Michael Andréw	1995
unige:9213	Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3	Lasseter, V. K.; Pulver, A. E.; Wolyniec, P. S.; Nestadt, G.; ... Kasch, L.	1995
unige:9217	Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain	Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A.	1995
unige:9262	The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells	Talbot, C. C.; Avramopoulos, D.; Gerken, S.; Chakravarti, A.; ... Antonarakis, Stylianos	1995
unige:9207	Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus	Karayiorgou, M.; Gogos, J. A.; Galke, B. L.; Jeffery, J. A.; ... Pulver, A. E.	1996
unige:9248	The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes	Pulver, A. E.; Wolyniec, P. S.; Housman, D.; Kazazian, H. H.; ... Kempf, L.	1996
unige:11222	Locations of human and mouse genes encoding the RFX1 and RFX2 transcription factor proteins	Doyle, J.; Hoffman, S.; Ucla, C.; Reith, Walter; ... Stubbs, L.	1996
unige:11624	Genetic linkage of IgG autoantibody production in relation to lupus nephritis in New Zealand hybrid mice	Vyse, T. J.; Drake, C. G.; Rozzo, S. J.; Roper, E.; ... Kotzin, B. L.	1996
unige:8680	Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3	Chen, H.; Rossier, Colette; Lalioti, M. D.; Lynn, A.; ... Antonarakis, Stylianos	1996
unige:8978	An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36	Radhakrishna, U.; Blouin, Jean-Louis; Solanki, J. V.; Dhoriani, G. M.; Antonarakis, Stylianos	1996
unige:9032	A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3	Sertie, A. L.; Quimby, M.; Moreira, E. S.; Murray, J.; ... Passos-Bueno, M. R.	1996

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