AAAAAA

   
Results: 1-5 |
Results: 5

Authors: CANKIKLAIN N RECAN D LLENSE S BARBOT JC LETURCQ F DEBURGRAVE N KAPLAN JC DEBEVEC M ZURAK N
Citation: N. Cankiklain et al., DIRECT MOLECULAR-GENETIC DIAGNOSIS AND CARRIER IDENTIFICATION IN ONE EMERY-DREIFUSS MUSCULAR-DYSTROPHY FAMILY, European journal of human genetics, 6, 1998, pp. 1033-1033

Authors: MANILAL S RECAN D SEWRY CA HOELTZENBEIN M LLENSE S LETURCQ F DEBURGRAVE N BARBOT JC MAN NT MUNTONI F WEHNERT M KAPLAN JC MORRIS GE
Citation: S. Manilal et al., MUTATIONS IN EMERY-DREIFUSS MUSCULAR-DYSTROPHY AND THEIR EFFECTS ON EMERIN PROTEIN EXPRESSION, Human molecular genetics, 7(5), 1998, pp. 855-864

Authors: MUNTONI F LICHTAROWICZKRYNSKA EJ SEWRY CA MANILAL S RECAN D LLENSE S TAYLOR J MORRIS GE DUBOWITZ V
Citation: F. Muntoni et al., EARLY PRESENTATION OF X-LINKED EMERY-DREIFUSS MUSCULAR-DYSTROPHY RESEMBLING LIMB-GIRDLE MUSCULAR-DYSTROPHY, Neuromuscular disorders, 8(2), 1998, pp. 72-76

Authors: ROMERO NB RECAN D RIGAL O LETURCQ F LLENSE S BARBOT JC DEBURGRAVE N CHEVAL MA DENIAU F KAPLAN JC
Citation: Nb. Romero et al., A POINT MUTATION IN THE GLYCEROL KINASE GENE ASSOCIATED WITH A DELETION IN THE DYSTROPHIN GENE IN A FAMILIAL X-LINKED MUSCULAR-DYSTROPHY - NONCONTIGUOUS GENE SYNDROME INVOLVING BECKER MUSCULAR-DYSTROPHY AND GLYCEROL KINASE LOCI, Neuromuscular disorders, 7(8), 1997, pp. 499-504

Authors: BILLUART P VINET MC PORTES VD LLENSE S RICHARD L MOUTARD ML RECAN D BRULS T BIENVENU T KAHN A BELDJORD C CHELLY J
Citation: P. Billuart et al., IDENTIFICATION BY STS PCR SCREENING OF A MICRODELETION IN XP21.3-22.1ASSOCIATED WITH NONSPECIFIC MENTAL-RETARDATION, Human molecular genetics, 5(7), 1996, pp. 977-979
Risultati: 1-5 |