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Results: 1-25 | 26-35 |
Results: 26-35/35
TAQI POLYMORPHISM IN INTRON-2 OF THE GCDH GENE
Authors: HAWORTH JC SINGAL R GOODMAN SI GREENBERG CR
Citation: Jc. Haworth et al., TAQI POLYMORPHISM IN INTRON-2 OF THE GCDH GENE, Human molecular genetics, 3(4), 1994, pp. 678-678
ASSIGNMENT OF HUMAN GLUTARYL-COA DEHYDROGENASE GENE (GCDH) TO THE SHORT ARM OF CHROMOSOME-19 (19P13.2) BY IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRID ANALYSIS
Authors: GREENBERG CR DUNCAN AMV GREGORY CA SINGAL R GOODMAN SI
Citation: Cr. Greenberg et al., ASSIGNMENT OF HUMAN GLUTARYL-COA DEHYDROGENASE GENE (GCDH) TO THE SHORT ARM OF CHROMOSOME-19 (19P13.2) BY IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRID ANALYSIS, Genomics, 21(1), 1994, pp. 289-290
LINKAGE ANALYSIS OF X-LINKED CLEFT-PALATE AND ANKYLOGLOSSIA IN MANITOBA MENNONITE AND BRITISH-COLUMBIA NATIVE KINDREDS
Authors: GORSKI SM ADAMS KJ BIRCH PH CHODIRKER BN GREENBERG CR GOODFELLOW PJ
Citation: Sm. Gorski et al., LINKAGE ANALYSIS OF X-LINKED CLEFT-PALATE AND ANKYLOGLOSSIA IN MANITOBA MENNONITE AND BRITISH-COLUMBIA NATIVE KINDREDS, Human genetics, 94(2), 1994, pp. 141-148
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
MOLECULAR CHARACTERIZATION OF CYTOGENETIC ALTERATIONS ASSOCIATED WITHTHE BECKWITH-WIEDEMANN SYNDROME (BWS) PHENOTYPE REFINES THE LOCALIZATION AND SUGGESTS THE GENE FOR BWS IS IMPRINTED
Authors: WEKSBERG R TESHIMA I WILLIAMS BRG GREENBERG CR PUESCHEL SM CHERNOS JE FOWLOW SB HOYME E ANDERSON IJ WHITEMAN DAH FISHER N SQUIRE J
Citation: R. Weksberg et al., MOLECULAR CHARACTERIZATION OF CYTOGENETIC ALTERATIONS ASSOCIATED WITHTHE BECKWITH-WIEDEMANN SYNDROME (BWS) PHENOTYPE REFINES THE LOCALIZATION AND SUGGESTS THE GENE FOR BWS IS IMPRINTED, Human molecular genetics, 2(5), 1993, pp. 549-556
A HOMOALLELIC GLY(317)-]ASP MUTATION IN ALPL CAUSES THE PERINATAL (LETHAL) FORM OF HYPOPHOSPHATASIA IN CANADIAN MENNONITES
Authors: GREENBERG CR TAYLOR CLD HAWORTH JC SEARGEANT LE PHILIPPS S TRIGGSRAINE B CHODIRKER BN
Citation: Cr. Greenberg et al., A HOMOALLELIC GLY(317)-]ASP MUTATION IN ALPL CAUSES THE PERINATAL (LETHAL) FORM OF HYPOPHOSPHATASIA IN CANADIAN MENNONITES, Genomics, 17(1), 1993, pp. 215-217
DOWN IN THE MORGUE
Authors: GREENBERG CR GREENBERG D
Citation: Cr. Greenberg et D. Greenberg, DOWN IN THE MORGUE, CMAJ. Canadian Medical Association journal, 149(5), 1993, pp. 542-542
IDENTIFICATION OF AN UNCOMMON HAPTOGLOBIN TYPE USING DNA AND PROTEIN-ANALYSIS
Authors: MARLES SL MCALPINE PJ ZELINSKI T PHILLIPS S MAEDA N GREENBERG CR
Citation: Sl. Marles et al., IDENTIFICATION OF AN UNCOMMON HAPTOGLOBIN TYPE USING DNA AND PROTEIN-ANALYSIS, Human genetics, 92(4), 1993, pp. 364-366
IMPROVED PREDICTIVE CARRIER TESTING FOR FAMILIAL ADENOMATOUS POLYPOSIS USING DNA FROM A SINGLE ARCHIVAL SPECIMEN AND POLYMORPHIC MARKERS WITH MULTIPLE ALLELES
Authors: BAPAT B MITRI A GREENBERG CR
Citation: B. Bapat et al., IMPROVED PREDICTIVE CARRIER TESTING FOR FAMILIAL ADENOMATOUS POLYPOSIS USING DNA FROM A SINGLE ARCHIVAL SPECIMEN AND POLYMORPHIC MARKERS WITH MULTIPLE ALLELES, Human pathology, 24(12), 1993, pp. 1376-1379
IMPACT OF GENETIC-COUNSELING AFTER NEONATAL SCREENING FOR DUCHENNE MUSCULAR-DYSTROPHY
Authors: HILDES E JACOBS HK CAMERON A SESHIA SS BOOTH F EVANS JA WROGEMANN K GREENBERG CR
Citation: E. Hildes et al., IMPACT OF GENETIC-COUNSELING AFTER NEONATAL SCREENING FOR DUCHENNE MUSCULAR-DYSTROPHY, Journal of Medical Genetics, 30(8), 1993, pp. 670-674
Risultati: 1-25 | 26-35 |