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Results: 1-25 | 26-27
Results: 1-25/27
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
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
GENE-MAPPING IN REGION 1Q42.1 AROUND A TRANSLOCATION BREAKPOINT ASSOCIATED WITH SCHIZOPHRENIA
Authors: ARVEILER B BOISSEAU P PETIT J TAINE L
Citation: B. Arveiler et al., GENE-MAPPING IN REGION 1Q42.1 AROUND A TRANSLOCATION BREAKPOINT ASSOCIATED WITH SCHIZOPHRENIA, American journal of medical genetics, 74(6), 1997, pp. 560-560
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
PRENATAL-DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS
Authors: GED C MOREAUGAUDRY F TAINE L HOMBRADOS I CALVAS P COLOMBIES P DEVERNEUIL H
Citation: C. Ged et al., PRENATAL-DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS, Prenatal diagnosis, 16(1), 1996, pp. 83-86
EXPANSION AND METHYLATION STATUS AT FRAXE CAN BE DETECTED ON ECORI BLOTS USED FOR FRAXA DIAGNOSIS - ANALYSIS OF 4 FRAXE FAMILIES WITH MILD MENTAL-RETARDATION IN MALES
Authors: BIANCALANA V TAINE L BOUIX JC FINCK S CHAUVIN A DEVERNEUIL H KNIGHT SJL STOLL C LACOMBE D MANDEL JL
Citation: V. Biancalana et al., EXPANSION AND METHYLATION STATUS AT FRAXE CAN BE DETECTED ON ECORI BLOTS USED FOR FRAXA DIAGNOSIS - ANALYSIS OF 4 FRAXE FAMILIES WITH MILD MENTAL-RETARDATION IN MALES, American journal of human genetics, 59(4), 1996, pp. 847-854
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
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
WHY CONFINE CHORIONIC VILLUS BIOPSY TO SINGLE PREGNANCIES
Authors: SAURA R TAINE L HOROVITZ J VERDIER G WEN ZQ ROUX D MAUGEY B VERGNAUD A
Citation: R. Saura et al., WHY CONFINE CHORIONIC VILLUS BIOPSY TO SINGLE PREGNANCIES, Prenatal diagnosis, 13(10), 1993, pp. 1009-1010
CHROMOSOME ANALYSIS OF ADENOMATOUS POLYPS OF THE COLON - POSSIBLE EXISTENCE OF 2 DIFFERENTLY EVOLVING CYTOGENETIC GROUPS
Authors: LONGY M SAURA R DUMAS F LESEVE JF TAINE L GOUSSOT JF COUZIGOU P
Citation: M. Longy et al., CHROMOSOME ANALYSIS OF ADENOMATOUS POLYPS OF THE COLON - POSSIBLE EXISTENCE OF 2 DIFFERENTLY EVOLVING CYTOGENETIC GROUPS, Cancer genetics and cytogenetics, 67(1), 1993, pp. 7-13
EXPERIENCE AND FETAL LOSS RATE IN TACVS
Authors: SAURA R GAUTHIER B TAINE L WEN ZQ HOROVITZ J ROUX D LAULOM B VERGNAUD A
Citation: R. Saura et al., EXPERIENCE AND FETAL LOSS RATE IN TACVS, American journal of human genetics, 53(3), 1993, pp. 1797-1797
Risultati: 1-25 | 26-27