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Results: 1-10 |
Results: 10
CONSERVED GENE STRUCTURE AND GENOMIC LINKAGE FOR D-DOPACHROME TAUTOMERASE (DDT) AND MIF
Authors: ESUMI N BUDARF M CICCARELLI L SELLINGER B KOZAK CA WISTOW G
Citation: N. Esumi et al., CONSERVED GENE STRUCTURE AND GENOMIC LINKAGE FOR D-DOPACHROME TAUTOMERASE (DDT) AND MIF, Mammalian genome, 9(9), 1998, pp. 753-757
CHARACTERIZATION OF 10P DELETIONS SUGGESTS 2 NONOVERLAPPING REGIONS CONTRIBUTE TO THE DIGEORGE-SYNDROME PHENOTYPE
Authors: GOTTLIEB S DRISCOLL DA PUNNETT HH SELLINGER B EMANUEL BS BUDARF ML
Citation: S. Gottlieb et al., CHARACTERIZATION OF 10P DELETIONS SUGGESTS 2 NONOVERLAPPING REGIONS CONTRIBUTE TO THE DIGEORGE-SYNDROME PHENOTYPE, American journal of human genetics, 62(2), 1998, pp. 495-498
LOCALIZATION OF THE HUMAN GENE FOR MACROPHAGE-MIGRATION INHIBITORY FACTOR (MIF) TO CHROMOSOME 22Q11.2
Authors: BUDARF M MCDONALD T SELLINGER B KOZAK C GRAHAM C WISTOW G
Citation: M. Budarf et al., LOCALIZATION OF THE HUMAN GENE FOR MACROPHAGE-MIGRATION INHIBITORY FACTOR (MIF) TO CHROMOSOME 22Q11.2, Genomics, 39(2), 1997, pp. 235-236
THE DIGEORGE-SYNDROME MINIMAL CRITICAL REGION CONTAINS A GOOSECOID-LIKE (GSCL) HOMEOBOX GENE THAT IS EXPRESSED EARLY IN HUMAN-DEVELOPMENT
Authors: GOTTLIEB S EMANUEL BS DRISCOLL DA SELLINGER B WANG ZL ROE B BUDARF ML
Citation: S. Gottlieb et al., THE DIGEORGE-SYNDROME MINIMAL CRITICAL REGION CONTAINS A GOOSECOID-LIKE (GSCL) HOMEOBOX GENE THAT IS EXPRESSED EARLY IN HUMAN-DEVELOPMENT, American journal of human genetics, 60(5), 1997, pp. 1194-1201
CLONING A BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME AND IDENTIFICATION OF A DISRUPTED CANDIDATE GENE
Authors: BUDARF ML COLLINS J GONG WL ROE B WANG ZL BAILEY LC SELLINGER B MICHAUD D DRISCOLL DA EMANUEL BS
Citation: Ml. Budarf et al., CLONING A BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME AND IDENTIFICATION OF A DISRUPTED CANDIDATE GENE, Nature genetics, 10(3), 1995, pp. 269-278
CLASSICAL NOONAN-SYNDROME IS NOT ASSOCIATED WITH DELETIONS OF 22Q11
Authors: ROBIN NH SELLINGER B MCDONALDMCGINN D ZACKAI EH EMANUEL BS DRISCOLL DA
Citation: Nh. Robin et al., CLASSICAL NOONAN-SYNDROME IS NOT ASSOCIATED WITH DELETIONS OF 22Q11, American journal of medical genetics, 56(1), 1995, pp. 94-96
CLONING A T(2-22)(Q14-Q11.21) BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME (DGS) AND IDENTIFICATION OF A DGS CANDIDATE LOCUS
Authors: BUDARF ML COLLINS J GONG W ROE B WANG Z BAILEY LC SELLINGER B MICHAUD D DRISCOLL DA EMANUEL BS
Citation: Ml. Budarf et al., CLONING A T(2-22)(Q14-Q11.21) BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME (DGS) AND IDENTIFICATION OF A DGS CANDIDATE LOCUS, American journal of human genetics, 57(4), 1995, pp. 56-56
MOLECULAR CHARACTERIZATION OF THE MARKER CHROMOSOME ASSOCIATED WITH CAT EYE SYNDROME
Authors: MEARS AJ DUNCAN AMV BUDARF ML EMANUEL BS SELLINGER B SIEGELBARTELT J GREENBERG CR MCDERMID HE
Citation: Aj. Mears et al., MOLECULAR CHARACTERIZATION OF THE MARKER CHROMOSOME ASSOCIATED WITH CAT EYE SYNDROME, American journal of human genetics, 55(1), 1994, pp. 134-142
PREVALENCE OF 22Q11 MICRODELETIONS IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES - IMPLICATIONS FOR GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS
Authors: DRISCOLL DA SALVIN J SELLINGER B BUDARF ML MCDONALDMCGINN DM ZACKAI EH EMANUEL BS
Citation: Da. Driscoll et al., PREVALENCE OF 22Q11 MICRODELETIONS IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES - IMPLICATIONS FOR GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS, Journal of Medical Genetics, 30(10), 1993, pp. 813-817
PRENATAL-DIAGNOSIS OF CAT EYE SYNDROME BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)
Authors: DRISCOLL DA SELLINGER B BUDARF ML EMANUEL BS MILLER RC DONNENFELD AE REESER SL
Citation: Da. Driscoll et al., PRENATAL-DIAGNOSIS OF CAT EYE SYNDROME BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH), American journal of human genetics, 53(3), 1993, pp. 1401-1401
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