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Results: 1-25/32
Authors:
AGULHON C
KOBETZ A
BLANCHET P
SARDA P
BIANCALANA V
SITTLER A
MALAFOSSE A
ABITHOL M
Citation: C. Agulhon et al., EXPRESSION OF FMR1, FXR1, AND FXR2 GENES IN HUMAN PRENATAL TISSUES, European journal of neuroscience, 10, 1998, pp. 9814-9814
Authors:
KLOSOWSKI S
DELOBEL B
MORISOT C
KONGOLO G
BIANCALANA V
THELLIEZ P
DJEBARA A
CROQUETTE MF
DEROUBAIX P
Citation: S. Klosowski et al., UNUSUAL MECHANISM IN PRADER-WILLI-SYNDROME - CONSEQUENCES FOR GENETIC-COUNSELING, Archives de pediatrie, 5(8), 1998, pp. 934-935
Authors:
NAGEL A
GRAF L
NAUMOV A
MARIOTTI E
BIANCALANA V
MESCHEDE D
WYNANDS R
Citation: A. Nagel et al., EXPERIMENTAL REALIZATION OF COHERENT DARK-STATE MAGNETOMETERS, Europhysics letters (Print), 44(1), 1998, pp. 31-36
Authors:
FRANKE P
LEBOYER M
GANSICKE M
WEIFFENBACH O
BIANCALANA V
CORNILLETLEFEBRE P
CROQUETTE MF
FROSTER U
SCHWAB SG
POUSTKA F
HAUTZINGER M
MAIER W
Citation: P. Franke et al., GENOTYPE-PHENOTYPE RELATIONSHIP IN FEMALE CARRIERS OF THE PREMUTATIONAND FULL MUTATION OF FMR-1, Psychiatry research, 80(2), 1998, pp. 113-127
Authors:
FRANKE P
LEBOYER M
WEIFFENBACH O
BIANCALANA V
CORNILLETLEFEBRE P
CROQUETTE MF
FROSTER U
SCHWAB SG
POUSTKA F
MAIER W
Citation: P. Franke et al., GENOTYPE-PHENOTYPE RELATIONSHIP IN FEMALE PRE-MUTATION AND FULL MUTATION FRA-X CARRIERS, American journal of medical genetics, 81(6), 1998, pp. 552-552
Authors:
MOUTOU C
VINCENT MC
BIANCALANA V
MANDEL JL
Citation: C. Moutou et al., TRANSITION FROM PREMUTATION TO FULL MUTATION IN FRAGILE-X-SYNDROME ISLIKELY TO BE PREZYGOTIC, Human molecular genetics, 6(7), 1997, pp. 971-979
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
Authors:
COUPRY I
IMBERT G
TAINE L
BOISSEAU P
BIANCALANA V
SAURA R
BATTIN J
MANDEL JL
LACOMBE D
ARVEILER B
Citation: I. Coupry et al., A 2ND CHOREA LOCUS ON CHROMOSOME-4, American journal of human genetics, 61(4), 1997, pp. 685-685
Authors:
MALZAC P
BIANCALANA V
VOELCKEL MA
MONCLA A
PELLISSIER MC
BOCCACCIO I
MATTEI JF
Citation: P. Malzac et al., UNEXPECTED INHERITANCE OF THE (CGG)(N) TRINUCLEOTIDE EXPANSION IN A FRAGILE-X SYNDROME FAMILY, European journal of human genetics, 4(1), 1996, pp. 8-12
Authors:
MALZAC P
BIANCALANA V
VOELCKEL MA
MONCLA A
PELLISSIER MC
BOCCACCIO I
MANDEL JL
MATTEI JF
Citation: P. Malzac et al., A RARE EXAMPLE OF A REVERSE MUTATION IN A FRAGILE-X SYNDROME FAMILY, American journal of medical genetics, 64(1), 1996, pp. 17-17
Authors:
BIANCALANA V
TAINE L
BOUIX JC
FINCK S
CHAUVIN A
DEVERNEUIL H
KNIGHT SJL
STOLL C
LACOMBE D
MANDEL JL
Citation: V. Biancalana et al., EXPANSION AND METHYLATION STATUS AT FRAXE CAN BE DETECTED ON ECORI BLOTS USED FOR FRAXA DIAGNOSIS - ANALYSIS OF 4 FRAXE FAMILIES WITH MILD MENTAL-RETARDATION IN MALES, American journal of human genetics, 59(4), 1996, pp. 847-854
Authors:
RUBINSZTEIN DC
LEGGO J
COLES R
ALMQVIST E
BIANCALANA V
CASSIMAN JJ
CHOTAI K
CONNARTY M
CRAUFURD D
CURTIS A
CURTIS D
DAVIDSON MJ
DIFFER AM
DODE C
DODGE A
FRONTALI M
RANEN NG
STINE OC
SHERR M
ABBOTT MH
FRANZ ML
GRAHAM CA
HARPER PS
HEDREEN JC
JACKSON A
KAPLAN JC
LOSEKOOT M
MACMILLAN JC
MORRISON P
TROTTIER Y
NOVELLETTO A
SIMPSON SA
THEILMANN J
WHITTAKER JL
FOLSTEIN SE
ROSS CA
HAYDEN MR
Citation: Dc. Rubinsztein et al., PHENOTYPIC CHARACTERIZATION OF INDIVIDUALS WITH 30-40 CAG REPEATS IN THE HUNTINGTON DISEASE (HD) GENE REVEALS HD CASES WITH 36 REPEATS AND APPARENTLY NORMAL ELDERLY INDIVIDUALS WITH 36-39 REPEATS, American journal of human genetics, 59(1), 1996, pp. 16-22
Authors:
CECCOTTI T
BASTIANI S
GIULIETTI A
BIANCALANA V
CHESSA P
GIULIETTI D
DANSON C
Citation: T. Ceccotti et al., A STUDY OF RANDOM PHASED LASER SPOTS, Laser and particle beams, 13(4), 1995, pp. 469-480
Authors:
DAHL N
LAPORTE J
HU LJ
BIANCALANA V
LEPASLIER D
COHEN D
PIUSSAN C
MANDEL JL
Citation: N. Dahl et al., DELETION MAPPING OF X-LINKED MIXED DEAFNESS (DFN3) IDENTIFIES A 265-525-KB REGION CENTROMERIC OF DXS26, American journal of human genetics, 56(4), 1995, pp. 999-1002
Authors:
PIUSSAN C
HANAUER A
DAHL N
MATHIEU M
KOLSKI C
BIANCALANA V
HEYBERGER S
STRUNSKI V
Citation: C. Piussan et al., X-LINKED PROGRESSIVE MIXED DEAFNESS - A NEW MICRODELETION THAT INVOLVES A MORE PROXIMAL REGION IN XQ21, American journal of human genetics, 56(1), 1995, pp. 224-230
Authors:
GIZZI LA
GIULIETTI D
GIULIETTI A
AFSHARRAD T
BIANCALANA V
CHESSA P
DANSON C
SCHIFANO E
VIANA SM
WILLI O
Citation: La. Gizzi et al., CHARACTERIZATION OF LASER PLASMAS FOR INTERACTION STUDIES (VOL 49, PG5628, 1994), Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics, 50(5), 1994, pp. 4266-4266
Authors:
GIZZI LA
GIULIETTI D
GIULIETTI A
AFSHARRAD T
BIANCALANA V
CHESSA P
DANSON C
SCHIFANO E
VIANA SM
WILLI O
Citation: La. Gizzi et al., CHARACTERIZATION OF LASER PLASMAS FOR INTERACTION STUDIES, Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics, 49(6), 1994, pp. 5628-5643
Authors:
RICHARDS RI
HOLMAN K
FRIEND K
STAPLES A
SUTHERLAND GR
OUDET C
BIANCALANA V
MANDEL JL
Citation: Ri. Richards et al., FRAXAC2 INSTABILITY, Nature genetics, 7(2), 1994, pp. 122-122
Authors:
BIANCALANA V
TRIVIER E
WEBER C
WEISSENBACH J
ROWE PSN
ORIORDAN JLH
PARTINGTON MW
HEYBERGER S
OUDET C
HANAUER A
Citation: V. Biancalana et al., CONSTRUCTION OF A HIGH-RESOLUTION LINKAGE MAP FOR XP22.1-P22.2 AND REFINEMENT OF THE GENETIC LOCALIZATION OF THE COFFIN-LOWRY SYNDROME GENE, Genomics, 22(3), 1994, pp. 617-625
Authors:
BATANI D
GIULIETTI A
BIANCALANA V
BIANCONI F
BORGHESI M
CHESSA P
GIULIETTI D
GIZZI L
DEHA I
SCHIFANO E
Citation: D. Batani et al., 2ND-HARMONIC LIGHT GENERATION IN THE INTERACTION OF LASER-BEAMS WITH UNDERCRITICAL PLASMAS, Physics essays, 7(1), 1994, pp. 87-94
Authors:
CHERY M
BIANCALANA V
PHILIPPE C
MALPUECH G
CARLA H
GILGENKRANTZ S
MANDEL JL
HANAUER A
Citation: M. Chery et al., HYPOMAGENSEMIA WITH SECONDARY HYPOCALCEMIA IN A FEMALE WITH BALANCED X9 TRANSLOCATION - MAPPING OF THE XP22 CHROMOSOME BREAKPOINT, Human genetics, 93(5), 1994, pp. 587-591
Authors:
ROWE PSN
GOULDING J
READ A
LEHRACH H
FRANCIS F
HANAUER A
OUDET C
BIANCALANA V
KOOH SW
DAVIES KE
ORIORDAN JLH
Citation: Psn. Rowe et al., REFINING THE GENETIC-MAP FOR THE REGION FLANKING THE X-LINKED HYPOPHOSPHATEMIC RICKETS LOCUS (XP22.1-22.2), Human genetics, 93(3), 1994, pp. 291-294
Authors:
DAHL N
BIANCALANA V
HANAUER A
HU L
LAPORTE J
LEPASLIER D
COHEN D
PIUSSAN C
MANDEL JL
Citation: N. Dahl et al., DELETION MAPPING OF THE DFN3 LOCUS AT XQ21.1, Cytogenetics and cell genetics, 67(4), 1994, pp. 336-336
Authors:
OUDET C
TRIVIER E
BIANCALANA V
HANAUER A
Citation: C. Oudet et al., REFINED PHYSICAL LOCALIZATION OF 4 GENES AND 2 EXPRESSED SEQUENCED TAGS (EST) IN THE XP22.2-]XP22.1 REGION, Cytogenetics and cell genetics, 67(4), 1994, pp. 357-358
Authors:
SCHIFANO E
BATON SD
BIANCALANA V
GIULIETTI A
GIULIETTI D
LABAUNE C
RENARD N
Citation: E. Schifano et al., 2ND-HARMONIC EMISSION FROM LASER-PREFORMED PLASMAS AS A DIAGNOSTIC FOR FILAMENTATION IN VARIOUS INTERACTION CONDITIONS, Laser and particle beams, 12(3), 1994, pp. 435-444