Citation: Y. Alembik et C. Stoll, A PATIENT WITH 13Q-SYNDROME WITH MILD MENTAL-RETARDATION AND WITH GROWTH-RETARDATION, European journal of human genetics, 6, 1998, pp. 2022-2022
Citation: C. Stoll et al., IMPACT OF ROUTINE FETAL ULTRASONOGRAPHIC SCREENING ON THE PREVALENCE OF DOWN-SYNDROME IN NON AGED MOTHERS, Annales de genetique, 41(1), 1998, pp. 27-30
Citation: Y. Alembik et al., IMPACT OF ROUTINE FETAL ULTRASONOGRAPHIC SCREENING ON THE PREVALENCE OF DOWN-SYNDROME IN NON AGED MOTHERS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 133-133
Authors:
MEDEIROS P
GILGENKRANTZ S
DEGEETER B
LIVOLSI A
GERAUDEL A
ALEMBIK Y
STOLL C
Citation: P. Medeiros et al., FURTHER DEMONSTRATION OF PHENOTYPIC HETEROGENEITY IN CHROMOSOME 22Q11.2 DELETION, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 252-252
Authors:
STOLL C
ROYDORAY B
GINGLINGER E
DOTT B
ALEMBIK Y
Citation: C. Stoll et al., ARE SOME MULTIPLE CONGENITAL-ANOMALIES THE CLINICAL EXPRESSION OF RARE AUTOSOMAL FRAGILE SITES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 281-281
Citation: C. Stoll et al., HEIGHT, WEIGHT AND OCCIPITO-FRONTAL CIRCUMFERENCE OF CHILDREN WITH DOWN-SYNDROME, Cytogenetics and cell genetics, 77, 1997, pp. 24-24
Citation: Y. Alembik et al., PREVALENCE OF NEURAL-TUBE DEFECTS IN NORTHEASTERN FRANCE, 1979-1994 IMPACT OF PRENATAL-DIAGNOSIS, Annales de genetique, 40(2), 1997, pp. 69-71
Citation: B. Dott et al., ARE SOME MULTIPLE CONGENITAL-ANOMALIES THE CLINICAL EXPRESSION OF RARE AUTOSOMAL FRAGILE SITES, American journal of human genetics, 61(4), 1997, pp. 694-694
Citation: C. Stoll et al., EVALUATION OF PRENATAL-DIAGNOSIS OF CONGENITAL GASTROINTESTINAL ATRESIAS, European journal of epidemiology, 12(6), 1996, pp. 611-616
Citation: C. Stoll et al., MULTIPLE FAMILIAL LIPOMATOSIS WITH POLYNEUROPATHY, AN INHERITED DOMINANT CONDITION, Annales de genetique, 39(4), 1996, pp. 193-196
Citation: C. Stoll et al., PRENATAL DETECTION OF INTERNAL URINARY SYSTEMS ANOMALIES - A REGISTRY-BASED STUDY, European journal of epidemiology, 11(3), 1995, pp. 283-290
Citation: C. Stoll et al., EVALUATION OF ROUTINE PRENATAL-DIAGNOSIS BY A REGISTRY OF CONGENITAL-ANOMALIES, Prenatal diagnosis, 15(9), 1995, pp. 791-800
Citation: C. Stoll et al., DISTRIBUTION OF SINGLE ORGAN MALFORMATIONS IN EUROPEAN POPULATIONS (VOL 38, PG 32, 1995), Annales de genetique, 38(4), 1995, pp. 216-216