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Results: 1-14 |
Results: 14
MOLECULAR AND CYTOGENETIC CHARACTERIZATION OF COMPLEMENTARY DELETION DUPLICATION INVOLVING THE SHORT ARM OF CHROMOSOME-7 DETECTED IN A FETUS AT AMNIOCENTESIS/
Authors: LAUNDON C VELAGALETI GVN EGGLESTON M TEAGUE K BUCHANAN P THARAPEL A
Citation: C. Laundon et al., MOLECULAR AND CYTOGENETIC CHARACTERIZATION OF COMPLEMENTARY DELETION DUPLICATION INVOLVING THE SHORT ARM OF CHROMOSOME-7 DETECTED IN A FETUS AT AMNIOCENTESIS/, Cytogenetics and cell genetics, 82(1-2), 1998, pp. 142-142
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
INFANT WITH MIDLINE THORACOABDOMINAL SCHISIS AND LIMB DEFECTS
Authors: PIVNICK EK KAUFMAN RA VELAGALETI GVN GUNTHER WM ABRAMOVICI D
Citation: Ek. Pivnick et al., INFANT WITH MIDLINE THORACOABDOMINAL SCHISIS AND LIMB DEFECTS, Teratology, 58(5), 1998, pp. 205-208
SIMULTANEOUS ADRENOCORTICAL CARCINOMA AND GANGLIONEUROBLASTOMA IN A CHILD WITH TURNER-SYNDROME AND GERMLINE P53 MUTATION
Authors: PIVNICK EK FURMAN WL VELAGALETI GVN JENKINS JJ CHASE NA RIBEIRO RC
Citation: Ek. Pivnick et al., SIMULTANEOUS ADRENOCORTICAL CARCINOMA AND GANGLIONEUROBLASTOMA IN A CHILD WITH TURNER-SYNDROME AND GERMLINE P53 MUTATION, Journal of Medical Genetics, 35(4), 1998, pp. 328-332
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
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
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
FAMILIAL DELETION OF CHROMOSOME-18 (P11.2)
Authors: VELAGALETI GVN HARRIS S CARPENTER NJ COLDWELL J SAY B
Citation: Gvn. Velagaleti et al., FAMILIAL DELETION OF CHROMOSOME-18 (P11.2), Annales de genetique, 39(4), 1996, pp. 201-204
Risultati: 1-14 |