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Results: 5

Authors: BITOUN P SEMINA E FERRELL RE MINTZHITTNER HA GAUDELUS J MURRAY JC
Citation: P. Bitoun et al., MUTATIONS IN PITX3 - A NOVEL HOMEOBOX TRANSCRIPTION FACTOR GENE HOMOLOGOUS TO RIEG1 CAUSE DOMINANT CATARACTS AND GLAUCOMA, European journal of human genetics, 6, 1998, pp. 401-401

Authors: ELSHANTI H MURRAY J SEMINA E BEUTOW K SCHERPBIER T ALALAMI J ALKHATIB A
Citation: H. Elshanti et al., THE ASSIGNMENT OF THE GENE RESPONSIBLE FOR PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA TO THE LONG ARM OF CHROMOSOME-6 AND EXAMINATION OF COL10A1 AS A CANDIDATE GENE, American journal of human genetics, 61(4), 1997, pp. 1596-1596

Authors: DATSON NA SEMINA E VANSTAALDUINEN AAA DAUWERSE HG MEERSHOEK EJ HEUS JJ FRANTS RR DENDUNNEN JT MURRAY JC VANOMMEN GJB
Citation: Na. Datson et al., CLOSING IN ON THE RIEGER SYNDROME GENE ON 4Q25 - MAPPING TRANSLOCATION BREAKPOINTS WITHIN A 50-KB REGION, American journal of human genetics, 59(6), 1996, pp. 1297-1305

Authors: GRAHAM JM HIXON H BACINO CA DAACKHIRSCH S SEMINA E MURRAY JC
Citation: Jm. Graham et al., AUTOSOMAL-DOMINANT TRANSMISSION OF A GOLDENHAR-LIKE SYNDROME WITH LINKAGE TO THE BRANCHIOOTORENAL SYNDROME LOCUS AT 8Q13, Pediatric research, 37(4), 1995, pp. 83-83

Authors: DATSON NA VANSTAALDUINEN AA SEMINA E MEERSHOEK EM HEUS JJ HOFKER MH MURRAY J FRANTS RR VANOMMEN GJB DENDUNNEN JT
Citation: Na. Datson et al., MAPPING TRANSLOCATION BREAKPOINTS IN RIEGER SYNDROME WITHIN A 200 KB REGION, American journal of human genetics, 57(4), 1995, pp. 1496-1496
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