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Results: 1-6 |
Results: 6

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
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