AAAAAA

   
Results: 1-9 |
Results: 9
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
CONNEXIN-26 GENE LINKED TO A DOMINANT DEAFNESS
Authors: DENOYELLE F LINAGRANADE G PLAUCHU H BRUZZONE R CHAIB H LEVIACOBAS F WEIL D PETIT C
Citation: F. Denoyelle et al., CONNEXIN-26 GENE LINKED TO A DOMINANT DEAFNESS, Nature, 393(6683), 1998, pp. 319-320
THE AUTOSOMAL RECESSIVE ISOLATED DEAFNESS, DFNB2, AND THE USHER 1B SYNDROME ARE ALLELIC DEFECTS OF THE MYOSIN-VIIA GENE
Authors: WEIL D KUSSEL P BLANCHARD S LEVY G LEVIACOBAS F DRIRA M AYADI H PETIT C
Citation: D. Weil et al., THE AUTOSOMAL RECESSIVE ISOLATED DEAFNESS, DFNB2, AND THE USHER 1B SYNDROME ARE ALLELIC DEFECTS OF THE MYOSIN-VIIA GENE, Nature genetics, 16(2), 1997, pp. 191-193
CLUSTERING OF MUTATIONS RESPONSIBLE FOR BRANCHIOOTORENAL (BOR) SYNDROME IN THE EYES ABSENT HOMOLOGOUS REGION (EYAHR) OF EYA1
Authors: ABDELHAK S KALATZIS V HEILIG R COMPAIN S SAMSON D VINCENT C LEVIACOBAS F CRUAUD C LEMERRER M MATHIEU M KONIG R VIGNERON J WEISSENBACH J PETIT C WEIL D
Citation: S. Abdelhak et al., CLUSTERING OF MUTATIONS RESPONSIBLE FOR BRANCHIOOTORENAL (BOR) SYNDROME IN THE EYES ABSENT HOMOLOGOUS REGION (EYAHR) OF EYA1, Human molecular genetics, 6(13), 1997, pp. 2247-2255
MYOSIN VIIA GENE - HETEROGENEITY OF THE MUTATIONS RESPONSIBLE FOR USHER-SYNDROME TYPE IB
Authors: LEVY G LEVIACOBAS F BLANCHARD S GERBER S LARGETPIET D CHENAL V LIU XZ NEWTON V STEEL KP BROWN SDM MUNNICH A KAPLAN J PETIT C WEIL D
Citation: G. Levy et al., MYOSIN VIIA GENE - HETEROGENEITY OF THE MUTATIONS RESPONSIBLE FOR USHER-SYNDROME TYPE IB, Human molecular genetics, 6(1), 1997, pp. 111-116
CLONING OF THE GENES ENCODING 2 MURINE AND HUMAN COCHLEAR UNCONVENTIONAL TYPE-I MYOSINS
Authors: CROZET F ELAMRAOUI A BLANCHARD S LENOIR M RIPOLL C VAGO P HAMEL C FIZAMES C LEVIACOBAS F DEPETRIS D MATTEI MG WEIL D PUJOL R PETIT C
Citation: F. Crozet et al., CLONING OF THE GENES ENCODING 2 MURINE AND HUMAN COCHLEAR UNCONVENTIONAL TYPE-I MYOSINS, Genomics, 40(2), 1997, pp. 332-341
HUMAN MYOSIN VIIA RESPONSIBLE FOR THE USHER 1B SYNDROME - A PREDICTEDMEMBRANE-ASSOCIATED MOTOR PROTEIN EXPRESSED IN DEVELOPING SENSORY EPITHELIA
Authors: WEIL D LEVY G SAHLY I LEVIACOBAS F BLANCHARD S ELAMRAOUI A CROZET F PHILIPPE H ABITBOL M PETIT C
Citation: D. Weil et al., HUMAN MYOSIN VIIA RESPONSIBLE FOR THE USHER 1B SYNDROME - A PREDICTEDMEMBRANE-ASSOCIATED MOTOR PROTEIN EXPRESSED IN DEVELOPING SENSORY EPITHELIA, Proceedings of the National Academy of Sciences of the United Statesof America, 93(8), 1996, pp. 3232-3237
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
DEFECTIVE MYOSIN VIIA GENE RESPONSIBLE FOR USHER SYNDROME TYPE 1B
Authors: WELL D BLANCHARD S KAPLAN J GUILFORD P GIBSON F WALSH J MBURU P VARELA A LEVILLERS J WESTON MD KELLEY PM KIMBERLING WJ WAGENAAR M LEVIACOBAS F LARGETPIET D MUNNICH A STEEL KP BROWN SDM PETIT C
Citation: D. Well et al., DEFECTIVE MYOSIN VIIA GENE RESPONSIBLE FOR USHER SYNDROME TYPE 1B, Nature, 374(6517), 1995, pp. 60-61
Risultati: 1-9 |