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Results: 1-8 |
Results: 8

Authors: BELIN V CUSIN V VIOT G GIRLICH D TOUTAIN A MONCLA A VEKEMANS M LEMERRER M MUNNICH A CORMIERDAIRE V
Citation: V. Belin et al., SHOX MUTATIONS IN DYSCHONDROSTEOSIS (LERI-WEILL-SYNDROME), Nature genetics, 19(1), 1998, pp. 67-69

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: FAIVRE L MORICHON N VIOT G MARTINOVIC J PINSON MP RACLIN V EDERY P DUMEZ Y MUNNICH A VEKEMANS M
Citation: L. Faivre et al., PRENATAL-DIAGNOSIS OF A CHROMOSOME 1P36 DELETION, European journal of human genetics, 6, 1998, pp. 2123-2123

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

Authors: VIOT G VEKEMANS M
Citation: G. Viot et M. Vekemans, THE NATURAL OUTCOME OF TRISOMY-21 MOSAICISM, Cytogenetics and cell genetics, 77, 1997, pp. 4-4

Authors: BANNATYNE R VIOT G
Citation: R. Bannatyne et G. Viot, USING HIGH-LEVEL LANGUAGES WITH MICROCONTROLLERS, Electronic engineering, 69(849), 1997, pp. 56-57

Authors: VIOT G VEKEMANS M
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
Risultati: 1-8 |