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Results:
1-12
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Results: 12
Authors:
SANLAVILLE D
LAPIERRE JM
BAUMANN C
ROMANA S
COLLOT N
TURLEAU C
TACHDJIAN G
Citation: D. Sanlaville et al., MOLECULAR CYTOGENETIC ANALYSIS OF A DE-NOVO DUPLICATION 9(P21PTER) AND GENOTYPE-PHENOTYPE CORRELATION, European journal of human genetics, 6, 1998, pp. 2108-2108
Authors:
MATHIEU M
PIUSSAN C
THEPOT F
GOUGET A
LACOMBE D
PEDESPAN JM
SERVILLE F
FONTAN D
RUFFIE M
NIVELONCHEVALLIER A
AMBLARD F
CHAUVEAU P
MOIROT H
CHABROLLE JP
CROQUETTE MF
TEYSSIER M
PLAUCHU H
PELISSIER MC
GILGENKRANTZ S
TURCCAREL C
TURLEAU C
PRIEUR M
LEMERRER M
GONZALES M
JOYE N
TAILLEMITE JL
BOUILLIE J
ESCHARD C
MOTTE J
JOURNEL H
Citation: M. Mathieu et al., COLLABORATIVE STUDY OF MOSAIC TETRASOMY 12P OR PALLISTER-KILLIAN-SYNDROME (19 FETUSES OR CHILDREN), Annales de genetique, 40(1), 1997, pp. 45-54
Authors:
BRIAULT S
VILLARD L
ODENT S
LUCAS J
RONCE N
TOUTAIN A
GUICHET A
LEMERRER M
TURLEAU C
MUNNICH A
FONTES M
MORAINE CL
Citation: S. Briault et al., PHYSICAL MAPPING OF THE BREAKPOINTS OF AN X-CHROMOSOME PARACENTRIC INVERSION INV(X) (Q11Q28) WHICH COSEGRATES WITH THE FG SYNDROME IN A FRENCH FAMILY, American journal of medical genetics, 64(1), 1996, pp. 20-20
Authors:
TURLEAU C
SIMONBOUY B
AUSTRUY E
GRISARD MC
LEMAIRE F
MOLINAGOMES D
SIFFROI JP
BOUE J
Citation: C. Turleau et al., PARENTAL ORIGIN AND MECHANISMS OF FORMATION OF 3 CASES OF 12P TETRASOMY, Clinical genetics, 50(1), 1996, pp. 41-46
Authors:
GUICHET A
BRIAULT S
MORAINE C
TURLEAU C
Citation: A. Guichet et al., TRISOMY-X - ACLF SOCIATION-DES-CYTOGENETICIENS-DE-LANGUE-FRANCAISE) RETROSPECTIVE STUDY, Annales de genetique, 39(3), 1996, pp. 117-122
Authors:
BLANQUET V
TURLEAU C
GROSSMORAND MS
BEAUFORT CS
DOZ F
BESMOND C
Citation: V. Blanquet et al., SPECTRUM OF GERMLINE MUTATIONS IN THE RB1 GENE - A STUDY OF 232 PATIENTS WITH HEREDITARY AND NON HEREDITARY RETINOBLASTOMA, Human molecular genetics, 4(3), 1995, pp. 383-388
Authors:
MATHIEU M
PIUSSAN C
THEPOT F
SERVILLE F
FONTA D
RUFFLER M
NIVELONCHEVALLIER A
TURCCAREL C
CHAUVEAU P
MOIROT H
CHABROLLE JP
MOTTE J
ESCHARD C
CROQUETTE MF
JOURNEL H
TURLEAU C
GOUGET A
PELISSIER MC
TEYSSIER M
PLAUCHU H
AMBLARD F
GILGENKRANZ S
LEMERRER M
PRIEUR M
Citation: M. Mathieu et al., IS PALLISTER-KILLIAN SYNDROME UNDERDIAGNOSED - A FRENCH COLLABORATIVESTUDY OF MOSAIC TETRASOMY 12P, American journal of human genetics, 57(4), 1995, pp. 532-532
Authors:
SALINAS CF
CANTU ES
PAI GS
TURLEAU C
Citation: Cf. Salinas et al., TRICHORHINOPHALANGEAL SYNDROME TYPE-II (LANGER-GIEDION) WITH BILATERAL AGENESIS OF TIBIA AND FIRST METATARSUS IN A BOY WITH 8Q INTERSTITIAL, American journal of human genetics, 57(4), 1995, pp. 560-560
Authors:
BLANQUET V
GROSS MS
TURLEAU C
SENAMAUDBEAUFORT C
DOZ F
BESMOND C
Citation: V. Blanquet et al., 3 NOVEL GERMLINE MUTATIONS IN EXON-8 AND EXON-18 OF THE RETINOBLASTOMA GENE, Human molecular genetics, 3(7), 1994, pp. 1185-1186
Authors:
BLANQUET V
TURLEAU C
GROSS MS
GOOSSENS M
BESMOND C
Citation: V. Blanquet et al., IDENTIFICATION OF GERMLINE MUTATIONS IN THE RB1 GENE BY DENATURANT GRADIENT GEL-ELECTROPHORESIS AND POLYMERASE CHAIN-REACTION DIRECT SEQUENCING, Human molecular genetics, 2(7), 1993, pp. 975-979
Authors:
JEANPIERRE M
TURLEAU C
AURIAS A
PRIEUR M
LEDEIST F
FISCHER A
VIEGASPEQUIGNOT E
Citation: M. Jeanpierre et al., AN EMBRYONIC-LIKE METHYLATION PATTERN OF CLASSICAL SATELLITE DNA IS OBSERVED IN ICF SYNDROME, Human molecular genetics, 2(6), 1993, pp. 731-735
Authors:
SAUGIERVEBER P
ABADIE V
MONCLA A
MATHIEU M
PIUSSAN C
TURLEAU C
MATTEI JF
MUNNICH A
LYONNET S
Citation: P. Saugierveber et al., THE JUBERG-MARSIDI SYNDROME MAPS TO THE PROXIMAL LONG ARM OF THE X-CHROMOSOME (XQ12-Q21), American journal of human genetics, 52(6), 1993, pp. 1040-1045
Risultati:
1-12
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