Authors:
CORMIERDAIRE V
LEMERRER M
GIGAREL N
MORICHON N
PRIEUR M
LYONNET S
VEKEMANS M
MUNNICH A
Citation: V. Cormierdaire et al., PREZYGOTIC ORIGIN OF THE ISOCHROMOSOME-12P IN PALLISTER-KILLIAN-SYNDROME, American journal of medical genetics, 69(2), 1997, pp. 166-168
Authors:
GIGAREL N
DEDREUZY P
THUILLIER L
ROCHETTE C
LENOIR G
MUNNICH A
BONNEFONT JP
Citation: N. Gigarel et al., A 26-KILOBASE DELETION SPANNING CFTR EXON-17A TO EXON-18 AND INTRON-19 IN CYSTIC-FIBROSIS (CF), American journal of human genetics, 61(4), 1997, pp. 2400-2400
Authors:
CORMIERDAIRE V
LEMERRER M
GIGAREL N
PRIEUR M
LYONNET S
MUNNICH A
Citation: V. Cormierdaire et al., PREZYGOTIC ORIGIN OF THE ISOCHROMOSOME-12P IN THE PALLISTER-KILLIAN-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 616-616
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