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Results: 1-21 |
Results: 21
ROBUST ADAPTIVE SLIDING MODE CONTROL WITH MODIFIED REGRESSOR MATRIX AND COMPOSITE ADAPTATION FOR ROBOTIC MANIPULATORS
Authors: CHONG SS YU XH MAN ZH
Citation: Ss. Chong et al., ROBUST ADAPTIVE SLIDING MODE CONTROL WITH MODIFIED REGRESSOR MATRIX AND COMPOSITE ADAPTATION FOR ROBOTIC MANIPULATORS, Advanced robotics, 12(1), 1998, pp. 53-66
GENOMIC ORGANIZATION OF THE MURINE MILLER-DIEKER LISSENCEPHALY REGION- CONSERVATION OF LINKAGE WITH THE HUMAN REGION/
Authors: HIROTSUNE S PACK SD CHONG SS ROBBINS CM PAVAN WJ LEDBETTER DH WYNSHAWBORIS A
Citation: S. Hirotsune et al., GENOMIC ORGANIZATION OF THE MURINE MILLER-DIEKER LISSENCEPHALY REGION- CONSERVATION OF LINKAGE WITH THE HUMAN REGION/, PCR methods and applications, 7(6), 1997, pp. 625-634
A REVISION OF THE LISSENCEPHALY AND MILLER-DIEKER SYNDROME CRITICAL REGIONS IN CHROMOSOME 17P13.3
Authors: CHONG SS PACK SD ROSCHKE AV TANIGAMI A CARROZZO R SMITH ACM DOBYNS WB LEDBETTER DH
Citation: Ss. Chong et al., A REVISION OF THE LISSENCEPHALY AND MILLER-DIEKER SYNDROME CRITICAL REGIONS IN CHROMOSOME 17P13.3, Human molecular genetics, 6(2), 1997, pp. 147-155
POINT MUTATIONS AND AN INTRAGENIC DELETION IN LIS1, THE LISSENCEPHALYCAUSATIVE GENE IN ISOLATED LISSENCEPHALY SEQUENCE AND MILLER-DIEKER SYNDROME
Authors: LONIGRO C CHONG SS SMITH ACM DOBYNS WB CARROZZO R LEDBETTER DH
Citation: C. Lonigro et al., POINT MUTATIONS AND AN INTRAGENIC DELETION IN LIS1, THE LISSENCEPHALYCAUSATIVE GENE IN ISOLATED LISSENCEPHALY SEQUENCE AND MILLER-DIEKER SYNDROME, Human molecular genetics, 6(2), 1997, pp. 157-164
CONTRIBUTION OF DNA-SEQUENCE AND CAG SIZE TO MUTATION FREQUENCIES OF INTERMEDIATE ALLELES FOR HUNTINGTON DISEASE - EVIDENCE FROM SINGLE SPERM ANALYSES
Authors: CHONG SS ALMQVIST E TELENIUS H LATRAY L NICHOL K BOURDELATPARKS B GOLDBERG YP HADDAD BR RICHARDS F SILLENCE D GREENBERG CR IVES E VANDENENGH G HUGHES MR HAYDEN MR
Citation: Ss. Chong et al., CONTRIBUTION OF DNA-SEQUENCE AND CAG SIZE TO MUTATION FREQUENCIES OF INTERMEDIATE ALLELES FOR HUNTINGTON DISEASE - EVIDENCE FROM SINGLE SPERM ANALYSES, Human molecular genetics, 6(2), 1997, pp. 301-309
DIFFERENT MUTATION-RATES OF SIMILAR SIZED CAG TRACTS OF AFFECTED HUNTINGTON-DISEASE CHROMOSOMES BY SINGLE SPERM ANALYSIS
Authors: ALMQVIST E CHONG SS NICHOL K TELENIUS H LATRAY L BOURDELATPARKS B HADDAD BR SQUITIERI F ANVRET M VANDENENGH G HAYDEN M
Citation: E. Almqvist et al., DIFFERENT MUTATION-RATES OF SIMILAR SIZED CAG TRACTS OF AFFECTED HUNTINGTON-DISEASE CHROMOSOMES BY SINGLE SPERM ANALYSIS, American journal of human genetics, 61(4), 1997, pp. 1768-1768
14-3-3-EPSILON HAS NO HOMOLOGY TO LIS1 AND LIES TELOMERIC TO IT ON CHROMOSOME 17P13.3 OUTSIDE THE MILLER-DIEKER SYNDROME CHROMOSOME REGION
Authors: CHONG SS TANIGAMI A ROSCHKE AV LEDBETTER DH
Citation: Ss. Chong et al., 14-3-3-EPSILON HAS NO HOMOLOGY TO LIS1 AND LIES TELOMERIC TO IT ON CHROMOSOME 17P13.3 OUTSIDE THE MILLER-DIEKER SYNDROME CHROMOSOME REGION, PCR methods and applications, 6(8), 1996, pp. 735-741
GAMETIC AND SOMATIC TISSUE-SPECIFIC HETEROGENEITY OF THE EXPANDED SCA1 CAG REPEAT IN SPINOCEREBELLAR ATAXIA TYPE-1
Authors: CHONG SS MCCALL AE COTA J SUBRAMONY SH ORR HT HUGHES MR ZOGHBI HY
Citation: Ss. Chong et al., GAMETIC AND SOMATIC TISSUE-SPECIFIC HETEROGENEITY OF THE EXPANDED SCA1 CAG REPEAT IN SPINOCEREBELLAR ATAXIA TYPE-1, Nature genetics, 10(3), 1995, pp. 344-350
CLONING, GENETIC-MAPPING, AND EXPRESSION ANALYSIS OF A MOUSE RENAL SODIUM-DEPENDENT PHOSPHATE COTRANSPORTER
Authors: CHONG SS KOZAK CA LIU LT KRISTJANSSON K DUNN ST BOURDEAU JE HUGHES MR
Citation: Ss. Chong et al., CLONING, GENETIC-MAPPING, AND EXPRESSION ANALYSIS OF A MOUSE RENAL SODIUM-DEPENDENT PHOSPHATE COTRANSPORTER, American journal of physiology. Renal, fluid and electrolyte physiology, 37(6), 1995, pp. 1038-1045
SINGLE-CELL ANALYSIS OF THE RHD BLOOD-TYPE FOR USE IN PREIMPLANTATIONDIAGNOSIS IN THE PREVENTION OF SEVERE HEMOLYTIC-DISEASE OF THE NEWBORN
Authors: VANDENVEYVER IB CHONG SS COTA J BENNETT PR FISK NM HANDYSIDE AH CARTRON JP LEVANKIM C COLIN Y SNABES MC MOISE KJ HUGHES MR
Citation: Ib. Vandenveyver et al., SINGLE-CELL ANALYSIS OF THE RHD BLOOD-TYPE FOR USE IN PREIMPLANTATIONDIAGNOSIS IN THE PREVENTION OF SEVERE HEMOLYTIC-DISEASE OF THE NEWBORN, American journal of obstetrics and gynecology, 172(2), 1995, pp. 533-540
SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS- APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1
Authors: HUGHES MR HADDAD BR SUBRAMANIAN S NASONKIN I COTA J CHONG SS
Citation: Mr. Hughes et al., SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS- APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1, American journal of human genetics, 57(4), 1995, pp. 152-152
GENETIC TYPING OF SINGLE CELLS USING MULTIPLE TETRAMERIC TANDEM REPEATS AFTER WHOLE GENOME AMPLIFICATION
Authors: HADDAD BR CHONG SS SUBRAMANIAN S COTA J HUGHES MR
Citation: Br. Haddad et al., GENETIC TYPING OF SINGLE CELLS USING MULTIPLE TETRAMERIC TANDEM REPEATS AFTER WHOLE GENOME AMPLIFICATION, American journal of human genetics, 57(4), 1995, pp. 156-156
SYSTEMATIC DELETION ANALYSIS OF MDS AND ILS PATIENTS EXCLUDES A CANDIDATE GENE AND DELINEATES THE LISSENCEPHALY GENE LOCUS
Authors: CHONG SS PACK S TANIGAMI A CARROZZO R DOBYNS WB LEDBETTER DH
Citation: Ss. Chong et al., SYSTEMATIC DELETION ANALYSIS OF MDS AND ILS PATIENTS EXCLUDES A CANDIDATE GENE AND DELINEATES THE LISSENCEPHALY GENE LOCUS, American journal of human genetics, 57(4), 1995, pp. 170-170
PREIMPLANTATION SINGLE-CELL ANALYSES OF DYSTROPHIN GENE DELETIONS USING WHOLE GENOME AMPLIFICATION
Authors: KRISTJANSSON K CHONG SS VANDENVEYVER IB SUBRAMANIAN S SNABES MC HUGHES MR
Citation: K. Kristjansson et al., PREIMPLANTATION SINGLE-CELL ANALYSES OF DYSTROPHIN GENE DELETIONS USING WHOLE GENOME AMPLIFICATION, Nature genetics, 6(1), 1994, pp. 19-23
ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE
Authors: CHONG SS EICHLER EE NELSON DL HUGHES MR
Citation: Ss. Chong et al., ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE, American journal of medical genetics, 51(4), 1994, pp. 522-526
PREIMPLANTATION SINGLE-CELL ANALYSIS OF MULTIPLE GENETIC-LOCI BY WHOLE-GENOME AMPLIFICATION
Authors: SNABES MC CHONG SS SUBRAMANIAN SB KRISTJANSSON K DISEPIO D HUGHES MR
Citation: Mc. Snabes et al., PREIMPLANTATION SINGLE-CELL ANALYSIS OF MULTIPLE GENETIC-LOCI BY WHOLE-GENOME AMPLIFICATION, Proceedings of the National Academy of Sciences of the United Statesof America, 91(13), 1994, pp. 6181-6185
MOLECULAR ANALYSIS OF HUMAN PLATELET ANTIGEN SYSTEM-1 ANTIGEN ON SINGLE CELLS CAN BE APPLIED TO PREIMPLANTATION GENETIC DIAGNOSIS FOR PREVENTION OF ALLOIMMUNE THROMBOCYTOPENIA
Authors: VANDENVEYVER IB CHONG SS KRISTJANSSON K SNABES MC MOISE KJ HUGHES MR
Citation: Ib. Vandenveyver et al., MOLECULAR ANALYSIS OF HUMAN PLATELET ANTIGEN SYSTEM-1 ANTIGEN ON SINGLE CELLS CAN BE APPLIED TO PREIMPLANTATION GENETIC DIAGNOSIS FOR PREVENTION OF ALLOIMMUNE THROMBOCYTOPENIA, American journal of obstetrics and gynecology, 170(3), 1994, pp. 807-812
PREIMPLANTATION PREVENTION OF X-LINKED DISEASE - RELIABLE AND RAPID SEX DETERMINATION OF SINGLE HUMAN-CELLS BY RESTRICTION ANALYSIS OF SIMULTANEOUSLY AMPLIFIED ZFX AND ZFY SEQUENCES
Authors: CHONG SS KRISTJANSSON K COTA J HANDYSIDE AH HUGHES MR
Citation: Ss. Chong et al., PREIMPLANTATION PREVENTION OF X-LINKED DISEASE - RELIABLE AND RAPID SEX DETERMINATION OF SINGLE HUMAN-CELLS BY RESTRICTION ANALYSIS OF SIMULTANEOUSLY AMPLIFIED ZFX AND ZFY SEQUENCES, Human molecular genetics, 2(8), 1993, pp. 1187-1191
MOLECULAR-CLONING OF THE CDNA-ENCODING A HUMAN RENAL SODIUM-PHOSPHATETRANSPORT PROTEIN AND ITS ASSIGNMENT TO CHROMOSOME 6P21.3-P23
Authors: CHONG SS KRISTJANSSON K ZOGHBI HY HUGHES MR
Citation: Ss. Chong et al., MOLECULAR-CLONING OF THE CDNA-ENCODING A HUMAN RENAL SODIUM-PHOSPHATETRANSPORT PROTEIN AND ITS ASSIGNMENT TO CHROMOSOME 6P21.3-P23, Genomics, 18(2), 1993, pp. 355-359
PREIMPLANTATION ANALYSIS FOR DYSTROPHIN GENE DELETIONS AFTER SINGLE-CELL GENOME PREAMPLIFICATION
Authors: CHONG SS KRISTJANSSON K VANDENVEYVER IB SNABES MC HUGHES MR
Citation: Ss. Chong et al., PREIMPLANTATION ANALYSIS FOR DYSTROPHIN GENE DELETIONS AFTER SINGLE-CELL GENOME PREAMPLIFICATION, American journal of human genetics, 53(3), 1993, pp. 1392-1392
A PREIMPLANTATION DIAGNOSTIC-APPROACH FOR THE PREVENTION OF NEONATAL ALLOIMMUNE THROMBOCYTOPENIC PURPURA
Authors: VANDENVEYVER IB CHONG SS MOISE KJ HUGHES MR
Citation: Ib. Vandenveyver et al., A PREIMPLANTATION DIAGNOSTIC-APPROACH FOR THE PREVENTION OF NEONATAL ALLOIMMUNE THROMBOCYTOPENIC PURPURA, American journal of human genetics, 53(3), 1993, pp. 1468-1468
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