Citation: S. Gilgenkrantz, ON CONNAIT LA CHANSON ... BUT SOME BETTER THAN OTHERS - THE ABSOLUTE PITCH PROCESSORS, MS. Medecine sciences, 14(5), 1998, pp. 671-672
Citation: A. Mignon et S. Gilgenkrantz, MEMBRANE-BOUND AND SOLUBLE FORM OF FAS LI GAND - A DANGEROUS CHOICE, MS. Medecine sciences, 14(4), 1998, pp. 511-514
Authors:
QUADERI NA
SCHWEIGER S
GAUDENZ K
FRANCO B
RUGARLI EI
BERGER W
FELDMAN GJ
VOLTA M
ANDOLFI G
GILGENKRANTZ S
MARION RW
HENNEKAM RCM
OPITZ JM
MUENKE M
ROPERS HH
BALLABIO A
Citation: Na. Quaderi et al., OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/, Nature genetics, 17(3), 1997, pp. 285-291
Authors:
COSSEE M
MOUTOU C
BIANCALANA V
BOUIX JC
PLESSIS G
DELOBEL B
CROQUETTE MF
GILGENKRANTZ S
LAMBERT JC
MALPUECH G
STOLL C
LANOE JL
PECHEVIS M
MANDEL JL
Citation: M. Cossee et al., THE FRAGILE-X-SYNDROME IS STILL UNDERDIAG NOSED - EFFICACY OF MOLECULAR TESTING IN MENTALLY-RETARDED PROBANDS, Archives de pediatrie, 4(3), 1997, pp. 227-236
Citation: B. Arveiler et S. Gilgenkrantz, AFTER THE YACS, HERE COME THE MAC HACS, HUMAN ARTIFICIAL CHROMOSOMES DIY/, MS. Medecine sciences, 13(8-9), 1997, pp. 1066-1068
Citation: S. Gilgenkrantz, 2 NEW HUMAN DEVELOPMENTAL GENES, TWIST AN D TBX5 INVOLVED IN SAETHRE-CHOTZEN AND IN HOLT-ORAM SYNDROMES, RESPECTIVELY, MS. Medecine sciences, 13(4), 1997, pp. 576-580
Citation: S. Gilgenkrantz, RIEGER SYNDROME - ANOTHER TRANSCRIPTION F ACTOR INVOLVED IN AN CRANIOFACIAL DYSMORPHIA, MS. Medecine sciences, 13(3), 1997, pp. 404-405