AAAAAA

   
Results: 1-8 |
Results: 8
THE FUNDAMENTAL AND MEDICAL IMPACTS OF RECENT PROGRESS IN RESEARCH ONHEREDITARY HEARING-LOSS
Authors: KALATZIS V PETIT C
Citation: V. Kalatzis et C. Petit, THE FUNDAMENTAL AND MEDICAL IMPACTS OF RECENT PROGRESS IN RESEARCH ONHEREDITARY HEARING-LOSS, Human molecular genetics (Print), 7(10), 1998, pp. 1589-1597
A HUMAN HOMOLOG OF THE DROSOPHILA EYES ABSENT GENE UNDERLIES BRANCHIOOTORENAL (BOR) SYNDROME AND IDENTIFIES A NOVEL GENE FAMILY
Authors: ABDELHAK S KALATZIS V HEILIG R COMPAIN S SAMSON D VINCENT C WEIL D CRUAUD C SAHLY I LEIBOVICI M BITNERGLINDZICZ M FRANCIS M LACOMBE D VIGNERON J CHARACHON R BOVEN K BEDBEDER P VANREGEMORTER N WEISSENBACH J PETIT C
Citation: S. Abdelhak et al., A HUMAN HOMOLOG OF THE DROSOPHILA EYES ABSENT GENE UNDERLIES BRANCHIOOTORENAL (BOR) SYNDROME AND IDENTIFIES A NOVEL GENE FAMILY, Nature genetics, 15(2), 1997, pp. 157-164
BOR AND BO SYNDROMES ARE ALLELIC DEFECTS OF EYA1
Authors: VINCENT C KALATZIS V ABDELHAK S CHAIB H COMPAIN S HELIAS J VANEECLOO FM PETIT C
Citation: C. Vincent et al., BOR AND BO SYNDROMES ARE ALLELIC DEFECTS OF EYA1, European journal of human genetics, 5(4), 1997, pp. 242-246
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
CHARACTERIZATION OF A TRANSLOCATION-ASSOCIATED DELETION DEFINES THE CANDIDATE REGION FOR THE GENE RESPONSIBLE FOR BRANCHIOOTORENAL SYNDROME(VOL 34, PG 422, 1996)
Authors: KALATZIS V ABDELHAK S COMPAIN S VINCENT C PETIT C
Citation: V. Kalatzis et al., CHARACTERIZATION OF A TRANSLOCATION-ASSOCIATED DELETION DEFINES THE CANDIDATE REGION FOR THE GENE RESPONSIBLE FOR BRANCHIOOTORENAL SYNDROME(VOL 34, PG 422, 1996), Genomics, 38(1), 1996, pp. 108-108
CHARACTERIZATION OF A TRANSLOCATION-ASSOCIATED DELETION DEFINES THE CANDIDATE REGION FOR THE GENE RESPONSIBLE FOR BRANCHIOOTORENAL SYNDROME
Authors: KALATZIS V ABDELHAK S COMPAIN S VINCENT C PETIT C
Citation: V. Kalatzis et al., CHARACTERIZATION OF A TRANSLOCATION-ASSOCIATED DELETION DEFINES THE CANDIDATE REGION FOR THE GENE RESPONSIBLE FOR BRANCHIOOTORENAL SYNDROME, Genomics, 34(3), 1996, pp. 422-425
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
MAPPING OF THE CHROMOSOME-11 BREAKPOINT OF THE T(4, 11)(Q21, P14-15) TRANSLOCATION
Authors: KALATZIS V PETERS GB DOBROVIC A
Citation: V. Kalatzis et al., MAPPING OF THE CHROMOSOME-11 BREAKPOINT OF THE T(4, 11)(Q21, P14-15) TRANSLOCATION, Cancer genetics and cytogenetics, 69(2), 1993, pp. 122-125
Risultati: 1-8 |