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Results: 1-25/30
Authors:
AYME S
URBERO B
OZIEL D
BISCARAT AC
GESNOUIN P
VAYSSEIX G
Citation: S. Ayme et al., ORPHANET - A DATABASE ON GENETIC-DISEASES AND GENETIC SERVICES IN FRANCE, European journal of human genetics, 6, 1998, pp. 1014-1014
Authors:
LEGEAI F
AYME S
Citation: F. Legeai et S. Ayme, NATURAL MORTALITY-RATE OF DOWN-SYNDROME FETUSES - A REAPPRAISAL USINGA DATABASE OF 4966 CASES, European journal of human genetics, 6, 1998, pp. 3067-3067
Authors:
DUMARET AC
DEVIGAN C
JULIANREYNIER C
GOUJARD J
ROSSET D
AYME S
Citation: Ac. Dumaret et al., ADOPTION AND FOSTERING OF BABIES WITH DOWN-SYNDROME - A COHORT OF 593CASES, Prenatal diagnosis, 18(5), 1998, pp. 437-445
Authors:
SIGAUDY S
TOUTAIN A
MONCLA A
FREDOUILLE C
BOURLIERE B
AYME S
PHILIP N
Citation: S. Sigaudy et al., MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM TAYBI-LINDER TYPE -REPORT OF 4 CASES AND REVIEW OF THE LITERATURE, American journal of medical genetics, 80(1), 1998, pp. 16-24
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
Authors:
CORDIER S
BERGERET A
GOUJARD J
HA MC
AYME S
BIANCHI F
CALZOLARI E
DEWALLE HEK
KNILLJONES R
CANDELA S
DALE I
DANANCHE B
DEVIGAN C
FEVOTTE J
KIEL G
MANDEREAU L
Citation: S. Cordier et al., CONGENITAL-MALFORMATIONS AND MATERNAL OCCUPATIONAL EXPOSURE TO GLYCOLETHERS, Epidemiology, 8(4), 1997, pp. 355-363
Authors:
AYME S
Citation: S. Ayme, GENOA MEETING - MAY 17, 1997, European journal of human genetics, 5(5), 1997, pp. 338-340
Authors:
AYME S
BRIARD ML
MATTEI JF
Citation: S. Ayme et al., GENETIC SERVICES IN FRANCE, European journal of human genetics, 5, 1997, pp. 76-80
Authors:
AYME S
MORICHON N
GOUJARD J
NISAND I
Citation: S. Ayme et al., PRENATAL-DIAGNOSIS IN FRANCE, European journal of human genetics, 5, 1997, pp. 26-31
Authors:
AYME S
PHILIP N
Citation: S. Ayme et N. Philip, APPARENTLY NEW SYNDROME OF CONGENITAL CATARACTS, SENSORINEURAL DEAFNESS, DOWN-SYNDROME-LIKE FACIAL APPEARANCE, SHORT STATURE, AND MENTAL-RETARDATION, American journal of medical genetics, 70(3), 1997, pp. 333-333
Authors:
SEROR V
COSTET N
LEGALES C
AYME S
Citation: V. Seror et al., ECONOMIC-ANALYSIS OF MATERNAL SERUM MARKERS SCREENING FOR DOWN-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 307-307
Authors:
AYME S
Citation: S. Ayme, PRENATAL-DIAGNOSIS OF DOWN-SYNDROME ACROS S EUROPE, MS. Medecine sciences, 12(3), 1996, pp. 393-396
Authors:
AYME S
Citation: S. Ayme, CONTRIBUTION OF REGISTRIES TO THE DECISIO N-PROCESS IN PUBLIC-HEALTH - THE EXAMPLE OF TRISOMY-21, Revue d'epidemiologie et de sante publique, 44, 1996, pp. 82-89
Authors:
DUMONTCEL ST
MENDIZABAL H
AYME S
LEVY A
PHILIP N
Citation: St. Dumontcel et al., PREVALENCE OF 22Q11 MICRODELETION, Journal of Medical Genetics, 33(8), 1996, pp. 719-719
Authors:
AYME S
PHILIP N
Citation: S. Ayme et N. Philip, POSSIBLE HOMOZYGOUS WAARDENBURG SYNDROME IN A FETUS WITH EXENCEPHALY, American journal of medical genetics, 59(2), 1995, pp. 263-265
Authors:
CALZOLARI E
BIANCHI F
DOLK H
MILAN M
LECHAT M
LEURQUIN P
GOYENS S
ASTOLFI G
VOLPATO S
AYME S
CALABRO A
CLEMENTI M
TENCONI R
CORNEL M
CUSCHIERI A
GARCIAMINAUR S
GARNE E
GILLEROT Y
GOUJARD J
HANSENKOENIG D
ROULLEAUX M
HOWARD PJ
JOHNSON Z
LILLIS DF
NEVIN NC
NELEN V
PEXIEDER T
PIERINI A
STOLL C
STONE DH
Citation: E. Calzolari et al., OMPHALOCELE AND GASTROSCHISIS IN EUROPE - A SURVEY OF 3-MILLION BIRTHS 1980-1990, American journal of medical genetics, 58(2), 1995, pp. 187-194
Authors:
RAMER JC
LIN AE
DOBYNS WB
WINTER R
AYME S
PALLOTTA R
LADDA RL
Citation: Jc. Ramer et al., PREVIOUSLY APPARENTLY UNDESCRIBED SYNDROME - SHALLOW ORBITS, PTOSIS, COLOBOMA, TRIGONOCEPHALY, GYRAL MALFORMATIONS, AND MENTAL AND GROWTH-RETARDATION, American journal of medical genetics, 57(3), 1995, pp. 403-409
Authors:
CONRATH J
DENIS D
LUCIANI A
BURGUIERE O
GAMBARELLI D
AYME S
PHILIP N
Citation: J. Conrath et al., WARBURG-WALKER SYNDROME - (REPORT OF 3 CASES), Vision research, 35, 1995, pp. 3128-3128
Authors:
JULIANREYNIER C
AURRAN Y
DUMARET A
MARON A
CHABAL F
GIRAUD F
AYME S
Citation: C. Julianreynier et al., ATTITUDES TOWARDS DOWNS-SYNDROME - FOLLOW-UP OF A COHORT OF 280 CASES, Journal of Medical Genetics, 32(8), 1995, pp. 597-599
Authors:
GILBERTDUSSARDIER B
BONNEAU D
GIGAREL N
LEMERRER M
BONNET D
PHILIP N
SERVILLE F
VERLOES A
ROSSI A
AYME S
WEISSENBACH J
MATTEI MG
LYONNET S
MUNNICH A
Citation: B. Gilbertdussardier et al., A NOVEL MICROSATELLITE DNA MARKER AT LOCUS D7S1870 DETECTS HEMIZYGOSITY IN 75-PERCENT OF PATIENTS WITH WILLIAMS-SYNDROME, American journal of human genetics, 56(2), 1995, pp. 542-544
Authors:
JULIANREYNIER C
MACQUARTMOULIN G
PHILIP N
SCHEINER C
POTIER A
GAMBARELLI D
AYME S
Citation: C. Julianreynier et al., FETAL ABNORMALITIES DETECTED BY SONOGRAPHY IN LOW-RISK PREGNANCIES - DISCREPANCIES BETWEEN PRE-TERMINATION AND POST-TERMINATION FINDINGS, Fetal diagnosis and therapy, 9(5), 1994, pp. 310-320
Authors:
AYME S
Citation: S. Ayme, REDUCING THE NUMBER OF AMNIOCENTESES IN WOMEN 35 YEARS OF AGE OR OLDER WITH MATERNAL SERUM MARKERS - COMMENTS, Revue d'epidemiologie et de sante publique, 42(5), 1994, pp. 468-469
Authors:
AYME S
Citation: S. Ayme, REDUCING THE NUMBER OF AMNIOCENTESES IN WOMEN 35 YEARS OF AGE OR OLDER WITH MATERNAL SERUM MARKERS - COMMENTS, Revue d'epidemiologie et de sante publique, 42(5), 1994, pp. 468-469
Authors:
JULIANREYNIER C
MACQUARTMOULIN G
MOATTI JP
AURRAN Y
CHABAL F
AYME S
Citation: C. Julianreynier et al., REASONS FOR WOMENS NON-UPTAKE OF AMNIOCENTESIS, Prenatal diagnosis, 14(9), 1994, pp. 859-864
Authors:
CORNEL MC
BREED ASPM
TENKATE LPL
MANTINGH A
AYME S
BECKER R
BIANCHI F
CALZOLARI E
CLEMENTI M
CUSCHIERI A
GARNE E
GILLEROT Y
GOUJARD J
HANSENKOENIG D
ROULLEAUX M
HOWARD PJ
JOHNSON Z
LAURENCE KM
LILLIS DF
MISSIOUTSANGARAKI S
NELEN V
NEVIN NC
PEXIEDER T
STOLL C
STONE DH
SVEL I
Citation: Mc. Cornel et al., VARIATION IN PRENATAL CYTOGENETIC DIAGNOSIS - POLICIES IN 13 EUROPEANCOUNTRIES, 1989-1991, Prenatal diagnosis, 14(5), 1994, pp. 337-344