Authors:
VIOT G
BRISSET S
FERT S
OZILOU C
ALLARD L
DEBLOIS MC
RAOUL O
LEMERRER M
LYONNET S
MUNNICH A
Citation: G. Viot et al., CHROMOSOME ANALYSIS ON FIBROBLASTS OF PATIENTS WITH MCA MR SYNDROME/, European journal of human genetics, 6, 1998, pp. 2099-2099
Authors:
ISERIN L
DELONLAY P
VIOT G
SIDI D
KACHANER J
MUNNICH A
LYONNET S
VEKEMANS M
BONNET D
Citation: L. Iserin et al., PREVALENCE OF THE MICRODELETION 22Q11 IN NEWBORN-INFANTS WITH CONGENITAL CONOTRUNCAL CARDIAC ANOMALIES, European journal of pediatrics, 157(11), 1998, pp. 881-884
Authors:
FAIVRE L
MORICHONDELVALLEZ N
VIOT G
NARCY F
LOISON S
MANDELBROT L
AUBRY MC
RACLIN V
EDERY P
MUNNICH A
VEKEMANS M
Citation: L. Faivre et al., PRENATAL-DIAGNOSIS OF AN 8P23.1 DELETION IN A FETUS WITH A DIAPHRAGMATIC-HERNIA AND REVIEW OF THE LITERATURE, Prenatal diagnosis, 18(10), 1998, pp. 1055-1060
Citation: G. Viot et M. Vekemans, THE NATURAL OUTCOME OF MOSAIC AND NONMOSAIC TRISOMY-21 ZYGOTES, American journal of human genetics, 61(4), 1997, pp. 2198-2198