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Citation: A. Gal et al., AFFINITY LABELING BY ATP AND GTP OF THE NUCLEAR-ENCODED OEC23 PROTEINOF THE PHOTOSYSTEM-II OXYGEN-EVOLVING COMPLEX, Journal of photochemistry and photobiology.B, Biology, 36(3), 1996, pp. 307-311
Citation: Sy. Xu et al., A 9TH LOCUS (RP18) FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA MAPS IN THE PERICENTROMERIC REGION OF CHROMOSOME-1, Human molecular genetics, 5(8), 1996, pp. 1193-1197
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Citation: A. Veske et al., AUTOSOMAL RECESSIVE NON-SYNDROMIC DEAFNESS LOCUS (DFNB8) MAPS ON CHROMOSOME 21Q22 IN A LARGE CONSANGUINEOUS KINDRED FROM PAKISTAN, Human molecular genetics, 5(1), 1996, pp. 165-168
Citation: D. Dori et al., A TEMPORAL DATABASE WITH DATA DEPENDENCIES - A KEY TO COMPUTER-INTEGRATED MANUFACTURING, International journal of computer integrated manufacturing, 9(2), 1996, pp. 89-104
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Citation: Sy. Xu et al., GENETIC-MAPPING OF RP1 ON 8Q11-Q21 IN AN AUSTRALIAN FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA REDUCES THE CRITICAL REGION TO 4 CMBETWEEN D8S601 AND D8S285, Human genetics, 98(6), 1996, pp. 741-743
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Citation: Js. Smolen et al., THE ROLE OF T-LYMPHOCYTES AND CYTOKINES IN RHEUMATOID-ARTHRITIS, Scandinavian journal of rheumatology, 25(1), 1996, pp. 1-4
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Citation: B. Wittwer et al., NEW X-LINKED MENTAL-RETARDATION SYNDROME WITH THE GENE MAPPED TENTATIVELY IN XP22.3, American journal of medical genetics, 64(1), 1996, pp. 42-49
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Citation: E. Schwinger et al., SHORT STATURE IN A MOTHER AND DAUGHTER WITH TERMINAL DELETION OF XP22.3, American journal of medical genetics, 63(1), 1996, pp. 239-242
Citation: Y. Wada et al., PHENOTYPIC CHARACTERISTICS OF PATIENTS WITH OGUCHIS-DISEASE ASSOCIATED WITH FREQUENT 1147DEL-A MUTATION IN THE ARRESTIN GENE, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4568-4568
Citation: A. Gal et Gn. Wogan, MUTAGENESIS ASSOCIATED WITH NITRIC-OXIDE PRODUCTION IN TRANSGENIC SJLMICE, Proceedings of the National Academy of Sciences of the United Statesof America, 93(26), 1996, pp. 15102-15107
Citation: A. Gal et al., NITRIC-OXIDE PRODUCTION IN SJL MICE BEARING THE RCSX LYMPHOMA - A MODEL FOR IN-VIVO TOXICOLOGICAL EVALUATION OF NO-CENTER-DOT, Proceedings of the National Academy of Sciences of the United Statesof America, 93(21), 1996, pp. 11499-11503
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Citation: Sm. Gu et al., 5 NOVEL MUTATIONS IN THE L1CAM GENE IN FAMILIES WITH X-LINKED HYDROCEPHALUS, Journal of Medical Genetics, 33(2), 1996, pp. 103-106
Citation: M. Nakazawa et al., VARIABLE EXPRESSIVITY IN A JAPANESE FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA CLOSELY LINKED TO CHROMOSOME 19Q, Archives of ophthalmology, 114(3), 1996, pp. 318-322
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VERGNAUD G
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Citation: Sa. Cox et al., EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES, Annals of Human Genetics, 60, 1996, pp. 447-486
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BUNGE S
BECK M
KRESSE H
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Citation: M. Rathmann et al., MUCOPOLYSACCHARIDOSIS TYPE-II (HUNTER SYNDROME) - MUTATION HOT-SPOTS IN THE IDURONATE-2-SULFATASE GENE, American journal of human genetics, 59(6), 1996, pp. 1202-1209
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Citation: K. Berezowski et al., CD5 IMMUNOREACTIVITY OF EPITHELIAL-CELLS IN THYMIC CARCINOMA AND CASTLE USING PARAFFIN-EMBEDDED TISSUE, American journal of clinical pathology, 106(4), 1996, pp. 483-486
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Citation: S. Fuchs et al., A HOMOZYGOUS 1-BASE PAIR DELETION IN THE ARRESTIN GENE IS A FREQUENT CAUSE OF OGUCHI DISEASE IN JAPANESE, Nature genetics, 10(3), 1995, pp. 360-362