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Results: 1-18 |
Results: 18
SEQUENCE CHARACTERIZATION OF A NEWLY IDENTIFIED HUMAN ALPHA-TUBULIN GENE (TUBA2)
Authors: DODE C WEIL D LEVILLIERS J CROZET F CHAIB H LEVIACOBAS F GUILFORD P PETIT C
Citation: C. Dode et al., SEQUENCE CHARACTERIZATION OF A NEWLY IDENTIFIED HUMAN ALPHA-TUBULIN GENE (TUBA2), Genomics, 47(1), 1998, pp. 125-130
ANOSMIN-1 UNDERLYING THE X-CHROMOSOME-LINKED KALLMANN-SYNDROME IS AN ADHESION MOLECULE THAT CAN MODULATE NEURITE GROWTH IN A CELL-TYPE-SPECIFIC MANNER
Authors: SOUSSIYANICOSTAS N FAIVRESARRAILH C HARDELIN JP LEVILLIERS J ROUGON G PETIT C
Citation: N. Soussiyanicostas et al., ANOSMIN-1 UNDERLYING THE X-CHROMOSOME-LINKED KALLMANN-SYNDROME IS AN ADHESION MOLECULE THAT CAN MODULATE NEURITE GROWTH IN A CELL-TYPE-SPECIFIC MANNER, Journal of Cell Science, 111, 1998, pp. 2953-2965
PRELINGUAL DEAFNESS - HIGH PREVALENCE OF A 30DELG MUTATION IN THE CONNEXIN 26 GENE
Authors: DENOYELLE F WEIL D MAW MA WILCOX SA LENCH NJ ALLENPOWELL DR OSBORN AH DAHL HHM MIDDLETON A HOUSEMAN MJ DODE C MARLIN S BOULILAELGGAIED A GRATI M AYADI H BENARAB S BITOUN P LINAGRANADE G GODET J MUSTAPHA M LOISELET J ELZIR E AUBOIS A JOANNARD A LEVILLIERS J GARABEDIAN EN MUELLER RF GARDNER RJM PETIT C
Citation: F. Denoyelle et al., PRELINGUAL DEAFNESS - HIGH PREVALENCE OF A 30DELG MUTATION IN THE CONNEXIN 26 GENE, Human molecular genetics, 6(12), 1997, pp. 2173-2177
INITIAL CHARACTERIZATION OF ANOSMIN-1, A PUTATIVE EXTRACELLULAR-MATRIX PROTEIN SYNTHESIZED BY DEFINITE NEURONAL CELL-POPULATIONS IN THE CENTRAL-NERVOUS-SYSTEM
Authors: SOUSSIYANICOSTAS N HARDELIN JP ARROYOJIMENEZ MD ARDOUIN O LEGOUIS R LEVILLIERS J TRAINCARD F BETTON JM CABANIE L PETIT C
Citation: N. Soussiyanicostas et al., INITIAL CHARACTERIZATION OF ANOSMIN-1, A PUTATIVE EXTRACELLULAR-MATRIX PROTEIN SYNTHESIZED BY DEFINITE NEURONAL CELL-POPULATIONS IN THE CENTRAL-NERVOUS-SYSTEM, Journal of Cell Science, 109, 1996, pp. 1749-1757
A YAC CONTIG AND AN EST MAP IN THE PERICENTROMERIC REGION OF CHROMOSOME-13 SURROUNDING THE LOCI FOR NEUROSENSORY NONSYNDROMIC DEAFNESS (DFNB1 AND DFNA3) AND LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C)
Authors: GUILFORD P DODE C CROZET F BLANCHARD S CHAIB H LEVILLIERS J LEVIACOBAS F WEIL D WEISSENBACH J COHEN D LEPASLIER D KAPLAN JC PETIT C
Citation: P. Guilford et al., A YAC CONTIG AND AN EST MAP IN THE PERICENTROMERIC REGION OF CHROMOSOME-13 SURROUNDING THE LOCI FOR NEUROSENSORY NONSYNDROMIC DEAFNESS (DFNB1 AND DFNA3) AND LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C), Genomics, 29(1), 1995, pp. 163-169
PREVALENCE AND MOLECULAR ANALYSIS OF 2 HOT-SPOTS FOR ECTOPIC RECOMBINATION LEADING TO XX MALENESS
Authors: WANG I WEIL D LEVILLIERS J AFFARA NA DELACHAPELLE A PETIT C
Citation: I. Wang et al., PREVALENCE AND MOLECULAR ANALYSIS OF 2 HOT-SPOTS FOR ECTOPIC RECOMBINATION LEADING TO XX MALENESS, Genomics, 28(1), 1995, pp. 52-58
HIGH-DENSITY PHYSICAL MAPPING OF A 3-MB REGION IN XP22.3 AND REFINED LOCALIZATION OF THE GENE FOR X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA (CDPX1)
Authors: WANG I FRANCO B FERRERO GB CHINAULT AC WEISSENBACH J CHUMAKOV I LEPASLIER D LEVILLIERS J KLINK A RAPPOLD GA BALLABIO A PETIT C
Citation: I. Wang et al., HIGH-DENSITY PHYSICAL MAPPING OF A 3-MB REGION IN XP22.3 AND REFINED LOCALIZATION OF THE GENE FOR X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA (CDPX1), Genomics, 26(2), 1995, pp. 229-238
THE X-CHROMOSOME-LINKED KALLMANNS-SYNDROME - THE KAL GENE IS INVOLVEDIN THE DEVELOPMENT OF THE CENTRAL OLFACTORY SYSTEM
Authors: LEGOUIS R HARDELIN JP LEVILLIERS J AYER C PETIT C
Citation: R. Legouis et al., THE X-CHROMOSOME-LINKED KALLMANNS-SYNDROME - THE KAL GENE IS INVOLVEDIN THE DEVELOPMENT OF THE CENTRAL OLFACTORY SYSTEM, Chemical senses, 20(1), 1995, pp. 178-179
HYPOGONADOTROPIC HYPOGONADISM WITH HYPOSMIA, X-LINKED ICHTHYOSIS, ANDRENAL MALFORMATION SYNDROME
Authors: MARTUL P PINEDA J LEVILLIERS J VAZQUEZ JA RODRIGUEZSORIANO J LORIDAN L DIAZPEREZ JL
Citation: P. Martul et al., HYPOGONADOTROPIC HYPOGONADISM WITH HYPOSMIA, X-LINKED ICHTHYOSIS, ANDRENAL MALFORMATION SYNDROME, Clinical endocrinology, 42(2), 1995, pp. 121-128
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY
Authors: FRANCO B MERONI G PARENTI G LEVILLIERS J BERNARD L GEBBIA M COX L MAROTEAUX P SHEFFIELD L RAPPOLD GA ANDRIA G PETIT C BALLABIO A
Citation: B. Franco et al., A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY, Cell, 81(1), 1995, pp. 15-25
A NON-SYNDROMIC FORM OF NEUROSENSORY, RECESSIVE DEAFNESS MAPS TO THE PERICENTROMERIC REGION OF CHROMOSOME-13Q
Authors: GUILFORD P BENARAB S BLANCHARD S LEVILLIERS J WEISSENBACH J BELKAHIA A PETIT C
Citation: P. Guilford et al., A NON-SYNDROMIC FORM OF NEUROSENSORY, RECESSIVE DEAFNESS MAPS TO THE PERICENTROMERIC REGION OF CHROMOSOME-13Q, Nature genetics, 6(1), 1994, pp. 24-28
A GENE RESPONSIBLE FOR A DOMINANT FORM OF NEUROSENSORY NON-SYNDROMIC DEAFNESS MAPS TO THE NSRD1 RECESSIVE DEAFNESS GENE INTERVAL
Authors: CHAIB H LINAGRANADE G GUILFORD P PLAUCHU H LEVILLIERS J MORGON A PETIT C
Citation: H. Chaib et al., A GENE RESPONSIBLE FOR A DOMINANT FORM OF NEUROSENSORY NON-SYNDROMIC DEAFNESS MAPS TO THE NSRD1 RECESSIVE DEAFNESS GENE INTERVAL, Human molecular genetics, 3(12), 1994, pp. 2219-2222
A PROPOSED NEW CONTIGUOUS GENE SYNDROME ON 8Q CONSISTS OF BRANCHIOOTORENAL (BOR) SYNDROME, DUANE SYNDROME, A DOMINANT FORM OF HYDROCEPHALUSAND TRAPEZE APLASIA - IMPLICATIONS FOR THE MAPPING OF THE BOR GENE
Authors: VINCENT C KALATZIS V COMPAIN S LEVILLIERS J SLIM R GRAIA F PEREIRA MD NIVELON A CROQUETTE MF LACOMBE D VIGNERON J HELIAS J BROYER M CALLEN DF HAAN EA WEISSENBACH J LACROIX B BELLANECHANTELOT C LEPASLIER D COHEN D PETIT C
Citation: C. Vincent et al., A PROPOSED NEW CONTIGUOUS GENE SYNDROME ON 8Q CONSISTS OF BRANCHIOOTORENAL (BOR) SYNDROME, DUANE SYNDROME, A DOMINANT FORM OF HYDROCEPHALUSAND TRAPEZE APLASIA - IMPLICATIONS FOR THE MAPPING OF THE BOR GENE, Human molecular genetics, 3(10), 1994, pp. 1859-1866
A 45,X MALE WITH AND X-Y TRANSLOCATION - IMPLICATIONS FOR THE MAPPINGOF THE GENES RESPONSIBLE FOR TURNER SYNDROME AND X-LINKED CHONDRODYSPLASIA-PUNCTATA
Authors: WEIL D PORTNOI MF LEVILLIERS J WANG I MATHIEU M TAILLEMITE JL MEIER M BOUDAILLIEZ B PETIT C
Citation: D. Weil et al., A 45,X MALE WITH AND X-Y TRANSLOCATION - IMPLICATIONS FOR THE MAPPINGOF THE GENES RESPONSIBLE FOR TURNER SYNDROME AND X-LINKED CHONDRODYSPLASIA-PUNCTATA, Human molecular genetics, 2(11), 1993, pp. 1853-1856
CHARACTERIZATION OF THE CHICKEN AND QUAIL HOMOLOGS OF THE HUMAN GENE RESPONSIBLE FOR THE X-LINKED KALLMANN SYNDROME
Authors: LEGOUIS R COHENSALMON M DELCASTILLO I LEVILLIERS J CAPY L MORNON JP PETIT C
Citation: R. Legouis et al., CHARACTERIZATION OF THE CHICKEN AND QUAIL HOMOLOGS OF THE HUMAN GENE RESPONSIBLE FOR THE X-LINKED KALLMANN SYNDROME, Genomics, 17(2), 1993, pp. 516-518
CONSTRUCTION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG SPANNING THE PSEUDOAUTOSOMAL REGION AND ISOLATION OF 25 NEW SEQUENCE-TAGGED SITES
Authors: SLIM R LEPASLIER D COMPAIN S LEVILLIERS J OUGEN P BILLAULT A DONOHUE SJ KLEIN DC MINTZ L BERNHEIM A COHEN D WEISSENBACH J PETIT C
Citation: R. Slim et al., CONSTRUCTION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG SPANNING THE PSEUDOAUTOSOMAL REGION AND ISOLATION OF 25 NEW SEQUENCE-TAGGED SITES, Genomics, 16(3), 1993, pp. 691-697
CONSTRUCTION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG SPANNING THE PSEUDOAUTOSOMAL REGION AND ISOLATION OF 25 NEW SEQUENCE-TAGGED SITES
Authors: SLIM R LEPASLIER D COMPAIN S LEVILLIERS J OUGEN P BILLAULT A DONOHUE SJ KLEIN DC MINTZ L BERNHEIM A COHEN D WEISSENBACH J PETIT C
Citation: R. Slim et al., CONSTRUCTION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG SPANNING THE PSEUDOAUTOSOMAL REGION AND ISOLATION OF 25 NEW SEQUENCE-TAGGED SITES, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 193-193
NO EVIDENCE FOR LINKAGE TO THE TYPE-1 OR TYPE-2 NEUROFIBROMATOSIS LOCI IN NOONAN SYNDROME FAMILIES
Authors: FLINTOFF WF BAHUAU M LYONNET S GILGENKRANTZ S LACOMBE D MARCON F LEVILLIERS J KACHANER J MUNNICH A LEMERRER M
Citation: Wf. Flintoff et al., NO EVIDENCE FOR LINKAGE TO THE TYPE-1 OR TYPE-2 NEUROFIBROMATOSIS LOCI IN NOONAN SYNDROME FAMILIES, American journal of medical genetics, 46(6), 1993, pp. 700-705
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