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Results: 1-25 | 26-34
Results: 1-25/34
SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT AND CHROMOSOME INSTABILITY
Authors: LACOMBE D TAINE L SAURA R
Citation: D. Lacombe et al., SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT AND CHROMOSOME INSTABILITY, European journal of human genetics, 6, 1998, pp. 1113-1113
REFINED LOCALIZATION OF THE VOLTAGE-GATED CHLORIDE CHANNEL, CLCN3, TO4Q33
Authors: TAINE L COUPRY I BOISSEAU P SAURA R LACOMBE D ARVEILER B
Citation: L. Taine et al., REFINED LOCALIZATION OF THE VOLTAGE-GATED CHLORIDE CHANNEL, CLCN3, TO4Q33, Human genetics, 102(2), 1998, pp. 178-181
FALSE-NEGATIVE RESULTS OF TRISOMY-21 ON DIRECT ANALYSIS ON CHORIONIC VILLUS SAMPLING
Authors: SAURA R ROUX D MAUGEYLAULON B TAINE L WEN ZQ VERGNAUD A HOROVITZ J
Citation: R. Saura et al., FALSE-NEGATIVE RESULTS OF TRISOMY-21 ON DIRECT ANALYSIS ON CHORIONIC VILLUS SAMPLING, Prenatal diagnosis, 18(8), 1998, pp. 866-867
SUBMICROSCOPIC DELETION OF CHROMOSOME 16P13.3 IN PATIENTS WITH RUBINSTEIN-TAYBI-SYNDROME
Authors: TAINE L GOIZET C WEN ZQ PETRIJ F BREUNING MH AYME S SAURA R ARVEILER B LACOMBE D
Citation: L. Taine et al., SUBMICROSCOPIC DELETION OF CHROMOSOME 16P13.3 IN PATIENTS WITH RUBINSTEIN-TAYBI-SYNDROME, American journal of medical genetics, 78(3), 1998, pp. 267-270
SAFETY AND FETAL-OUTCOME OF EARLY AND MIDTRIMESTER AMNIOCENTESIS
Authors: SAURA R TAINE L GUYON F MANGIONE R HOROVITZ J
Citation: R. Saura et al., SAFETY AND FETAL-OUTCOME OF EARLY AND MIDTRIMESTER AMNIOCENTESIS, Lancet, 351(9113), 1998, pp. 1434-1435
ESOPHAGEAL ATRESIA, VACTERL ASSOCIATION - FANCONIS ANEMIA RELATED SPECTRUM OF ANOMALIES
Authors: PEREL Y BUTENANDT O CARRERE A SAURA R FAYON M LAMIREAU T VERGNES P
Citation: Y. Perel et al., ESOPHAGEAL ATRESIA, VACTERL ASSOCIATION - FANCONIS ANEMIA RELATED SPECTRUM OF ANOMALIES, Archives of Disease in Childhood, 78(4), 1998, pp. 375-376
QUALITY GUIDELINES AND STANDARDS FOR GENETIC LABORATORIES CLINICS IN PRENATAL-DIAGNOSIS ON FETAL SAMPLES OBTAINED BY INVASIVE PROCEDURES - AN ATTEMPT TO ESTABLISH A COMMON EUROPEAN FRAMEWORK FOR QUALITY ASSESSMENT/
Authors: KROISEL PM FRYNS JP MATTHIJS G BRONDUMNIELSEN K VEJERSLEV L VONKOSKULL H GIRAUDON E SAURA R HELD K MULLERREIBLE CR METAXOTOU C GENUARDI M PIOMBO G SCHNEIDER F SMEETS D VANDENOUWELAND A PACHECO P CORREIA H BINKERT F GABARRON J GALLANO P KRISTOFFERSSON U ANVRET M HOWELL R STENHOUSE S
Citation: Pm. Kroisel et al., QUALITY GUIDELINES AND STANDARDS FOR GENETIC LABORATORIES CLINICS IN PRENATAL-DIAGNOSIS ON FETAL SAMPLES OBTAINED BY INVASIVE PROCEDURES - AN ATTEMPT TO ESTABLISH A COMMON EUROPEAN FRAMEWORK FOR QUALITY ASSESSMENT/, European journal of human genetics, 5(6), 1997, pp. 342-350
FIRST-TRIMESTER NUCHAL TRANSLUCENCY AND CYSTIC HYGROMA - A RISK A RISK ANALYSIS ON FETAL CHROMOSOME ABNORMALITY - A REPORT ON 183 CASES
Authors: SAURA R LECHAT X TAINE L WEN ZQ GUYON F HOROVITZ J
Citation: R. Saura et al., FIRST-TRIMESTER NUCHAL TRANSLUCENCY AND CYSTIC HYGROMA - A RISK A RISK ANALYSIS ON FETAL CHROMOSOME ABNORMALITY - A REPORT ON 183 CASES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 81-81
FETOPLACENTAL DISCREPANCIES - LITERATURE-REVIEW (CONCERNING 36,981 TESTS)
Authors: SAURA R TAINE L WEN ZQ GUYON F HOROVITZ J
Citation: R. Saura et al., FETOPLACENTAL DISCREPANCIES - LITERATURE-REVIEW (CONCERNING 36,981 TESTS), Cytogenetics and cell genetics, 77(1-2), 1997, pp. 182-182
MATERNAL HETERODISOMY-16 AND INTRAUTERINE GROWTH-RETARDATION (IUGR)
Authors: SAURA R TAINE L WEN ZQ GUYON F HOROVITZ J
Citation: R. Saura et al., MATERNAL HETERODISOMY-16 AND INTRAUTERINE GROWTH-RETARDATION (IUGR), Cytogenetics and cell genetics, 77(1-2), 1997, pp. 183-183
CHORIONIC VILLUS SAMPLING AND MATERNAL CELL CONTAMINATION ON LONG-TERM CULTURE
Authors: SAURA R RUIZ B TAINE L WEN ZQ GUYON F HOROVITZ J
Citation: R. Saura et al., CHORIONIC VILLUS SAMPLING AND MATERNAL CELL CONTAMINATION ON LONG-TERM CULTURE, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 184-184
FREQUENCY OF 16P13.3 SUBMICROSCOPIC DELETIONS IN FRENCH PATIENTS WITHRUBINSTEIN-TAYBI-SYNDROME
Authors: TAINE L GOIZET C WEN ZQ PETRIJ F BREUNING M SAURA R ARVEILER B LACOMBE D
Citation: L. Taine et al., FREQUENCY OF 16P13.3 SUBMICROSCOPIC DELETIONS IN FRENCH PATIENTS WITHRUBINSTEIN-TAYBI-SYNDROME, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 284-284
18P MONOSOMY WITH MIDLINE DEFECTS AND A DE-NOVO SATELLITE IDENTIFIED BY FISH
Authors: TAINE L GOIZET C WEN ZQ CHATEIL JF BATTIN J SAURA R LACOMBE D
Citation: L. Taine et al., 18P MONOSOMY WITH MIDLINE DEFECTS AND A DE-NOVO SATELLITE IDENTIFIED BY FISH, Annales de genetique, 40(3), 1997, pp. 158-163
SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT, AND CHROMOSOME INSTABILITY
Authors: LACOMBE D TAINE L SAURA R
Citation: D. Lacombe et al., SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT, AND CHROMOSOME INSTABILITY, American journal of human genetics, 61(4), 1997, pp. 583-583
A 2ND CHOREA LOCUS ON CHROMOSOME-4
Authors: COUPRY I IMBERT G TAINE L BOISSEAU P BIANCALANA V SAURA R BATTIN J MANDEL JL LACOMBE D ARVEILER B
Citation: I. Coupry et al., A 2ND CHOREA LOCUS ON CHROMOSOME-4, American journal of human genetics, 61(4), 1997, pp. 685-685
APOPTOSIS OF BOVINE ARTICULAR CHONDROCYTES INDUCED BY PROSTAGLANDIN-E2
Authors: MIWA M SAURA R HIRATA S ISHIKAWA H MIZUNO K
Citation: M. Miwa et al., APOPTOSIS OF BOVINE ARTICULAR CHONDROCYTES INDUCED BY PROSTAGLANDIN-E2, Arthritis and rheumatism, 39(9), 1996, pp. 1449-1449
PRENATAL-DIAGNOSIS OF TRISOMY-9 - 6 CASES AND A REVIEW OF THE LITERATURE
Authors: SAURA R TRAORE W TAINE L WEN ZQ ROUX D MAUGEYLAULOM B RUFFIE M VERGNAUD A HOROVITZ J
Citation: R. Saura et al., PRENATAL-DIAGNOSIS OF TRISOMY-9 - 6 CASES AND A REVIEW OF THE LITERATURE, Prenatal diagnosis, 15(7), 1995, pp. 609-614
FIRST TRIMESTER DIAGNOSIS OF FETAL NUCHAL EDEMA - REPORT OF 29 CASES
Authors: BRUN JL SAURA R HOROVITZ J MAUGEY B TAINE L ROUX D VERGNAUD A
Citation: Jl. Brun et al., FIRST TRIMESTER DIAGNOSIS OF FETAL NUCHAL EDEMA - REPORT OF 29 CASES, Fetal diagnosis and therapy, 9(4), 1994, pp. 246-251
AMNIOTIC-FLUID LEAKAGE AND MISCARRIAGES AFTER TA-CVS
Authors: SAURA R TAINE L WEN ZQ TRAORE W HOROVITZ J
Citation: R. Saura et al., AMNIOTIC-FLUID LEAKAGE AND MISCARRIAGES AFTER TA-CVS, Prenatal diagnosis, 14(9), 1994, pp. 897-897
IS NON-ECHOGENIC NUCHAL EDEMA A MARKER IN TRISOMY-21 SCREENING
Authors: SAURA R BRUN JL TAINE L HOROVITZ J MAUGEY B ROUX D
Citation: R. Saura et al., IS NON-ECHOGENIC NUCHAL EDEMA A MARKER IN TRISOMY-21 SCREENING, Prenatal diagnosis, 14(1), 1994, pp. 69-70
OPERATOR EXPERIENCE AND FETAL LOSS RATE IN TRANSABDOMINAL CVS
Authors: SAURA R GAUTHIER B TAINE L WEN ZQ HOROVITZ J ROUX D LAULOM B VERGNAUD A
Citation: R. Saura et al., OPERATOR EXPERIENCE AND FETAL LOSS RATE IN TRANSABDOMINAL CVS, Prenatal diagnosis, 14(1), 1994, pp. 70-71
INHIBITION OF NEOVASCULARIZATION IN-VIVO BY GOLD COMPOUNDS
Authors: SAURA R MATSUBARA T MIZUNO K
Citation: R. Saura et al., INHIBITION OF NEOVASCULARIZATION IN-VIVO BY GOLD COMPOUNDS, Rheumatology international, 14(1), 1994, pp. 1-7
EARLY AMNIOCENTESIS VERSUS CHORIONIC VILLUS SAMPLING FOR FETAL KARYOTYPING
Authors: SAURA R ROUX D TAINE L MAUGEY B LAULON D LAPLACE JP HOROVITZ J
Citation: R. Saura et al., EARLY AMNIOCENTESIS VERSUS CHORIONIC VILLUS SAMPLING FOR FETAL KARYOTYPING, Lancet, 344(8925), 1994, pp. 825-826
C-MITOTIC AGGREGATIONS RESULT FROM FAILURE OF CYTOKINESIS
Authors: CHAMLA Y SAURA R
Citation: Y. Chamla et R. Saura, C-MITOTIC AGGREGATIONS RESULT FROM FAILURE OF CYTOKINESIS, Annales de genetique, 37(1), 1994, pp. 39-41
GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES
Authors: BOESPFLUGTANGUY O MIMAULT C MELKI J CAVAGNA A GIRAUD G DINH DP DASTUGUE B DAUTIGNY A AICARDI J GOUTTIERES F BAUMANN N BERTINI E DAVID A HENOCQ A LANDRIEU P TARDIEU M LEBERRE C LEMAREC B LYON G MAYER M PINARD JM PONSOT G MATHIEU M SAINTIVE JP SAURA R VALLEE L
Citation: O. Boespflugtanguy et al., GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES, American journal of human genetics, 55(3), 1994, pp. 461-467
Risultati: 1-25 | 26-34