Authors:
MUSTAPHA M
CHARDENOUX S
NIEDER A
SALEM N
WEISSENBACH J
ELZIR E
LOISELET J
PETIT C
Citation: M. Mustapha et al., A SENSORINEURAL PROGRESSIVE AUTOSOMAL RECESSIVE FORM OF ISOLATED DEAFNESS, DFNB13, MAPS TO CHROMOSOME 7Q34-Q36, European journal of human genetics, 6(3), 1998, pp. 245-250
Authors:
SAOUDA M
MANSOUR A
MOGLABEY YB
ELZIR E
MUSTAPHA M
CHAIB H
NEHME A
MEGARBANE A
LOISELET J
PETIT C
SLIM R
Citation: M. Saouda et al., THE USHER-SYNDROME IN THE LEBANESE POPULATION AND FURTHER REFINEMENT OF THE USH2A CANDIDATE REGION, Human genetics, 103(2), 1998, pp. 193-198
Authors:
MOUGLABEY YB
NIMRI S
SAYEGH F
ELZIR E
SLIM R
Citation: Yb. Mouglabey et al., MAP REFINEMENT OF THE USHER-SYNDROME TYPE 1B GENE, MYO7A, RELATIVE TO11Q13.5 MICROSATELLITE MARKERS, Clinical genetics, 54(2), 1998, pp. 155-158
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
Authors:
CHAIB H
PLACE C
SALEM N
DODE C
CHARDENOUX S
WEISSENBACH J
ELZIR E
LOISELET J
PETIT C
Citation: H. Chaib et al., MAPPING OF DFNB12, A GENE FOR A NON-SYNDROMAL AUTOSOMAL RECESSIVE DEAFNESS, TO CHROMOSOME 10Q21-22, Human molecular genetics, 5(7), 1996, pp. 1061-1064
Authors:
CHAIB H
PLACE C
SALEM N
CHARDENOUX S
VINCENT C
WEISSENBACH J
ELZIR E
LOISELET J
PETIT C
Citation: H. Chaib et al., A GENE RESPONSIBLE FOR A SENSORINEURAL NONSYNDROMIC RECESSIVE DEAFNESS MAPS TO CHROMOSOME 2P22-23, Human molecular genetics, 5(1), 1996, pp. 155-158