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Results: 1-25 | 26-29
Results: 1-25/29
RAPID ASSESSMENT OF AMNIOTIC-FLUID BY PRIMED IN-SITU LABELING (PRINS)FOR SUSPECTED FETAL TRISOMY-18
Authors: SHULMAN LP VELAGELATI GPVN PHILLIPS OP THARAPEL AT
Citation: Lp. Shulman et al., RAPID ASSESSMENT OF AMNIOTIC-FLUID BY PRIMED IN-SITU LABELING (PRINS)FOR SUSPECTED FETAL TRISOMY-18, Prenatal diagnosis, 18(2), 1998, pp. 189-190
MOST JACOBSEN-SYNDROME DELETION BREAKPOINTS OCCUR DISTAL TO FRA11B
Authors: MICHAELIS RC VELAGALETI GVN JONES C PIVNICK EK PHELAN MC BOYD E TARLETON J WILROY RS TUNNACLIFFE A THARAPEL AT
Citation: Rc. Michaelis et al., MOST JACOBSEN-SYNDROME DELETION BREAKPOINTS OCCUR DISTAL TO FRA11B, American journal of medical genetics, 76(3), 1998, pp. 222-228
PRENATAL KARYOTYPING USING FETAL BLOOD OBTAINED BY CORDOCENTESIS - RAPID AND ACCURATE RESULTS WITHIN 24 HOURS
Authors: THARAPEL SA DEV VG SHULMAN LP THARAPEL AT
Citation: Sa. Tharapel et al., PRENATAL KARYOTYPING USING FETAL BLOOD OBTAINED BY CORDOCENTESIS - RAPID AND ACCURATE RESULTS WITHIN 24 HOURS, Annales de genetique, 41(2), 1998, pp. 69-72
PRIMED IN-SITU LABELING FOR RAPID PRENATAL-DIAGNOSIS
Authors: VELAGELATI GVN SHULMAN LP PHILLIPS OP THARAPEL SA THARAPEL AT
Citation: Gvn. Velagelati et al., PRIMED IN-SITU LABELING FOR RAPID PRENATAL-DIAGNOSIS, American journal of obstetrics and gynecology, 178(6), 1998, pp. 1313-1317
ISCN-1995 - GUIDELINES FOR IN-SITU HYBRIDIZATION NOMENCLATURE
Authors: THARAPEL AT
Citation: At. Tharapel, ISCN-1995 - GUIDELINES FOR IN-SITU HYBRIDIZATION NOMENCLATURE, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 37-37
CLINICAL AND CYTOGENETIC OUTCOME IN 2,305 FIRST-TRIMESTER CHORIONIC VILLUS SAMPLING PATIENTS
Authors: MARTENS PR SHULMAN LP PHILLIPS OP SEELY LM VELAGALETI GVN THARAPEL AT
Citation: Pr. Martens et al., CLINICAL AND CYTOGENETIC OUTCOME IN 2,305 FIRST-TRIMESTER CHORIONIC VILLUS SAMPLING PATIENTS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 164-164
CONFIRMATION OF FETAL ANEUPLOIDY WITH PRIMED IN-SITU HYBRIDIZATION ONAMNIOTIC-FLUID DURING SELECTIVE FETAL REDUCTION
Authors: PHILLIPS OP VELAGALETI GVN EMERSON DE THARAPEL AT SHULMAN LP
Citation: Op. Phillips et al., CONFIRMATION OF FETAL ANEUPLOIDY WITH PRIMED IN-SITU HYBRIDIZATION ONAMNIOTIC-FLUID DURING SELECTIVE FETAL REDUCTION, Prenatal diagnosis, 17(6), 1997, pp. 586-588
DISCORDANT DIRECT AND CULTURE RESULTS FOLLOWING CHORIONIC VILLUS SAMPLING AND THE DIAGNOSIS OF A 3RD CELL-LINE IN THE FETUS
Authors: PHILLIPS OP VELAGALETI GVN THARAPEL AT SHULMAN LP
Citation: Op. Phillips et al., DISCORDANT DIRECT AND CULTURE RESULTS FOLLOWING CHORIONIC VILLUS SAMPLING AND THE DIAGNOSIS OF A 3RD CELL-LINE IN THE FETUS, Prenatal diagnosis, 17(2), 1997, pp. 170-172
RAPID IDENTIFICATION OF MARKER CHROMOSOMES USING PRIMED IN-SITU LABELING (PRINS)
Authors: VELAGALETI GVN THARAPEL SA MARTENS PR THARAPEL AT
Citation: Gvn. Velagaleti et al., RAPID IDENTIFICATION OF MARKER CHROMOSOMES USING PRIMED IN-SITU LABELING (PRINS), American journal of medical genetics, 71(2), 1997, pp. 130-133
DOWN-SYNDROME WITH BIPARENTAL INHERITANCE OF DER(14Q21Q) AND MATERNALLY DERIVED TRISOMY-21 - CONFIRMATION BY FLUORESCENT IN-SITU HYBRIDIZATION AND MICROSATELLITE POLYMORPHISM ANALYSIS
Authors: RAJANGAM S MICHAELIS RC VELAGALETI GVN LINCOLN S HEGDE S LEWIN S TARLETON J THOMAS IM THARAPEL AT
Citation: S. Rajangam et al., DOWN-SYNDROME WITH BIPARENTAL INHERITANCE OF DER(14Q21Q) AND MATERNALLY DERIVED TRISOMY-21 - CONFIRMATION BY FLUORESCENT IN-SITU HYBRIDIZATION AND MICROSATELLITE POLYMORPHISM ANALYSIS, American journal of medical genetics, 70(1), 1997, pp. 43-47
CLINICAL-APPLICATIONS OF PRIMED IN-SITU LABELING (PRINS) RAPID IDENTIFICATION OF A MARKER CHROMOSOME IN A FETUS
Authors: VELAGALETI GVN CARPENTER NJ THARAPEL AT
Citation: Gvn. Velagaleti et al., CLINICAL-APPLICATIONS OF PRIMED IN-SITU LABELING (PRINS) RAPID IDENTIFICATION OF A MARKER CHROMOSOME IN A FETUS, Annales de genetique, 40(3), 1997, pp. 154-157
BACKGROUND IN-SITU HYBRIDIZATION SIGNALS IN INTERPHASE NUCLEI CAN BE EXPLAINED BY ASYNCHRONOUS REPLICATION OF DNA AT HOMOLOGOUS LOCI
Authors: KADANDALE JS SHULMAN LP PHILLIPS OP THARAPEL SA VELAGALETI GVN THARAPEL AT
Citation: Js. Kadandale et al., BACKGROUND IN-SITU HYBRIDIZATION SIGNALS IN INTERPHASE NUCLEI CAN BE EXPLAINED BY ASYNCHRONOUS REPLICATION OF DNA AT HOMOLOGOUS LOCI, American journal of human genetics, 61(4), 1997, pp. 730-730
RAPID PRENATAL-DIAGNOSIS BY PRIMED IN-SITU LABELING (PRINS)
Authors: PHILLIPS OP VELAGELATI GVN SHULMAN LP THARAPEL SA MARTENS PR WACHTEL SS THARAPEL AT
Citation: Op. Phillips et al., RAPID PRENATAL-DIAGNOSIS BY PRIMED IN-SITU LABELING (PRINS), American journal of human genetics, 61(4), 1997, pp. 918-918
PHYSICAL MAPPING OF SEQUENCE-TAGGED SITES (STS) ON HUMAN-CHROMOSOME-11 USING THE PRINS-CARD METHOD
Authors: VELAGALETI GVN CORNWELL D TROYER DL MARTENS PR THARAPEL AT
Citation: Gvn. Velagaleti et al., PHYSICAL MAPPING OF SEQUENCE-TAGGED SITES (STS) ON HUMAN-CHROMOSOME-11 USING THE PRINS-CARD METHOD, American journal of human genetics, 61(4), 1997, pp. 1430-1430
A JUMPING ROBERTSONIAN TRANSLOCATION - A MOLECULAR AND CYTOGENETIC STUDY
Authors: GROSS SJ THARAPEL AT PHILLIPS OP SHULMAN LP PIVNICK EK PARK VM
Citation: Sj. Gross et al., A JUMPING ROBERTSONIAN TRANSLOCATION - A MOLECULAR AND CYTOGENETIC STUDY, Human genetics, 98(3), 1996, pp. 291-296
JACOBSEN-SYNDROME - REPORT OF A PATIENT WITH SEVERE EYE ANOMALIES, GROWTH-HORMONE DEFICIENCY, AND HYPOTHYROIDISM ASSOCIATED WITH DELETION-11(Q23Q25) AND REVIEW OF 52 CASES
Authors: PIVNICK EK VELAGALETI GVN WILROY RS SMITH ME ROSE SR TIPTON RE THARAPEL AT
Citation: Ek. Pivnick et al., JACOBSEN-SYNDROME - REPORT OF A PATIENT WITH SEVERE EYE ANOMALIES, GROWTH-HORMONE DEFICIENCY, AND HYPOTHYROIDISM ASSOCIATED WITH DELETION-11(Q23Q25) AND REVIEW OF 52 CASES, Journal of Medical Genetics, 33(9), 1996, pp. 772-778
RISK OF FETAL MOSAICISM WHEN PLACENTAL MOSAICISM IS DIAGNOSED BY CHORIONIC VILLUS SAMPLING
Authors: PHILLIPS OP THARAPEL AT LERNER JL PARK VM WACHTEL SS SHULMAN LP
Citation: Op. Phillips et al., RISK OF FETAL MOSAICISM WHEN PLACENTAL MOSAICISM IS DIAGNOSED BY CHORIONIC VILLUS SAMPLING, American journal of obstetrics and gynecology, 174(3), 1996, pp. 850-855
A JUMPING ROBERTSONIAN TRANSLOCATION - CHARACTERIZATION OF CHROMOSOMESEGREGATION AND CHROMOSOME STRUCTURE
Authors: PARK VM GROSS S THARAPEL AT PHILLIPS OP SHULMAN LP
Citation: Vm. Park et al., A JUMPING ROBERTSONIAN TRANSLOCATION - CHARACTERIZATION OF CHROMOSOMESEGREGATION AND CHROMOSOME STRUCTURE, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 115-115
CHARACTERIZATION OF AN UNBALANCED DE-NOVO REARRANGEMENT BY MICROSATELLITE POLYMORPHISM TYPING AND BY FLUORESCENT IN-SITU HYBRIDIZATION
Authors: ZHAO J GORDON PL WILROY RS MARTENS PR TARLETON J SHULMAN LP SIMPSON JL ELIAS S THARAPEL AT
Citation: J. Zhao et al., CHARACTERIZATION OF AN UNBALANCED DE-NOVO REARRANGEMENT BY MICROSATELLITE POLYMORPHISM TYPING AND BY FLUORESCENT IN-SITU HYBRIDIZATION, American journal of medical genetics, 56(4), 1995, pp. 398-402
DEFINING THE PRECISE BREAKPOINTS IN DEL(11Q) BY MICROSATELLITE POLYMORPHISM AND IN-SITU HYBRIDIZATION (ISH)
Authors: MICHAELIS RC PIVNICK EK GOPALRAO VVN WILROY RS TARLETON J PATIL SR THARAPEL AT
Citation: Rc. Michaelis et al., DEFINING THE PRECISE BREAKPOINTS IN DEL(11Q) BY MICROSATELLITE POLYMORPHISM AND IN-SITU HYBRIDIZATION (ISH), American journal of human genetics, 57(4), 1995, pp. 675-675
DOWN-SYNDROME (DS) WITH HOMOZYGOUS T(14Q21Q) AND NONDISJUNCTION TRISOMY-21 - ASSIGNMENT OF BIPARENTAL ORIGIN OF T(14Q21) CHROMOSOMES AND MATERNAL ORIGIN OF THE EXTRA 21 BY MICROSATELLITE POLYMORPHISM
Authors: RAJANGAM S MICHAELIS RC THOMAS IM LINCOLN S HEGDE S LEWIN S TARLETON J THARAPEL AT
Citation: S. Rajangam et al., DOWN-SYNDROME (DS) WITH HOMOZYGOUS T(14Q21Q) AND NONDISJUNCTION TRISOMY-21 - ASSIGNMENT OF BIPARENTAL ORIGIN OF T(14Q21) CHROMOSOMES AND MATERNAL ORIGIN OF THE EXTRA 21 BY MICROSATELLITE POLYMORPHISM, American journal of human genetics, 57(4), 1995, pp. 691-691
RISK OF FETAL MOSAICISM WHEN PLACENTAL MOSAICISM IS DIAGNOSED BY CHORIONIC VILLUS SAMPLING
Authors: PHILLIPS OP THARAPEL AT PARK VM WACHTEL SS SHULMAN LP
Citation: Op. Phillips et al., RISK OF FETAL MOSAICISM WHEN PLACENTAL MOSAICISM IS DIAGNOSED BY CHORIONIC VILLUS SAMPLING, American journal of human genetics, 57(4), 1995, pp. 1667-1667
MOLECULAR ANALYSIS TO ASSIGN PARENTAL ORIGIN AND DISTINGUISH DE-NOVO I(21Q) FROM T(21Q21Q) IN 2 DOWN-SYNDROME FETUSES
Authors: ZHAO J THARAPEL AT SHULMAN LP SIMPSON JL ELIAS S
Citation: J. Zhao et al., MOLECULAR ANALYSIS TO ASSIGN PARENTAL ORIGIN AND DISTINGUISH DE-NOVO I(21Q) FROM T(21Q21Q) IN 2 DOWN-SYNDROME FETUSES, Journal of the Society for Gynecologic Investigation, 1(2), 1994, pp. 128-130
INABILITY TO DETECT FETAL METAPHASES IN FLOW-SORTED LYMPHOCYTE-CULTURES BASED ON MATERNAL-FETAL HLA DIFFERENCES
Authors: THARAPEL AT JASWANEY VL DOCKTER ME WACHTEL SS CHANDLER RW SIMPSON JL SHULMAN LP MEYERS CM ELIAS S
Citation: At. Tharapel et al., INABILITY TO DETECT FETAL METAPHASES IN FLOW-SORTED LYMPHOCYTE-CULTURES BASED ON MATERNAL-FETAL HLA DIFFERENCES, Fetal diagnosis and therapy, 8(2), 1993, pp. 95-101
VERY RAPID PRENATAL KARYOTYPIC ANALYSIS USING UNCULTURED FETAL NUCLEATED RED BLOOD
Authors: SHULMAN LP MERCER BM MARTENS P THARAPEL AT
Citation: Lp. Shulman et al., VERY RAPID PRENATAL KARYOTYPIC ANALYSIS USING UNCULTURED FETAL NUCLEATED RED BLOOD, Prenatal diagnosis, 13(12), 1993, pp. 1153-1156
Risultati: 1-25 | 26-29