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Results: 1-8 |
Results: 8
INABILITY TO INDUCE FRAGILE SITES AT CTG REPEATS IN CONGENITAL MYOTONIC-DYSTROPHY
Authors: WENGER SL GIANGRECO CA TARLETON J WESSEL HB
Citation: Sl. Wenger et al., INABILITY TO INDUCE FRAGILE SITES AT CTG REPEATS IN CONGENITAL MYOTONIC-DYSTROPHY, American journal of medical genetics, 66(1), 1996, pp. 60-63
GENETIC AND BIOCHEMICAL NORMALIZATION IN FEMALE CARRIERS OF DUCHENNE MUSCULAR-DYSTROPHY - EVIDENCE FOR FAILURE OF DYSTROPHIN PRODUCTION IN DYSTROPHIN-COMPETENT MYONUCLEI
Authors: PEGORARO E SCHIMKE RN GARCIA C STERN H CADALDINI M ANGELINI C BARBOSA E CARROLL J MARKS WA NEVILLE HE MARKS H APPLETON S TORIELLO H WESSEL HB DONNELLY J BERNES SM TABER JW WEISS L HOFFMAN EP
Citation: E. Pegoraro et al., GENETIC AND BIOCHEMICAL NORMALIZATION IN FEMALE CARRIERS OF DUCHENNE MUSCULAR-DYSTROPHY - EVIDENCE FOR FAILURE OF DYSTROPHIN PRODUCTION IN DYSTROPHIN-COMPETENT MYONUCLEI, Neurology, 45(4), 1995, pp. 677-690
NO FRAGILITY AT TRINUCLEOTIDE REPEATS IN CONGENITAL MYOTONIC-DYSTROPHY
Authors: WENGER SL GIANGRECO CA TARLETON J WESSEL HB
Citation: Sl. Wenger et al., NO FRAGILITY AT TRINUCLEOTIDE REPEATS IN CONGENITAL MYOTONIC-DYSTROPHY, American journal of human genetics, 57(4), 1995, pp. 730-730
REGURGITANT REFLUX, VS NON-REGURGITANT REFLUX, IS PRECEDED BY RECTUS-ABDOMINIS CONTRACTION IN INFANTS
Authors: ORENSTEIN SR DENT J DENEAULT LG LUTZ JW WESSEL HB KELSEY SF SHALABY TM
Citation: Sr. Orenstein et al., REGURGITANT REFLUX, VS NON-REGURGITANT REFLUX, IS PRECEDED BY RECTUS-ABDOMINIS CONTRACTION IN INFANTS, Neurogastroenterology and motility, 6(4), 1994, pp. 271-277
GENETIC NORMALIZATION IN DUCHENNE CARRIERS
Authors: PEGORARO E SCHIMKE RN ARAHATA K HIYASHI Y STERN H MARKS H GLASBERG MR CARROLL JE TABER JW WESSEL HB BAUSERMAN SC TORIELLO HV APPLETON S SCHWARTZ LS GARCIA CA HOFFMAN EP
Citation: E. Pegoraro et al., GENETIC NORMALIZATION IN DUCHENNE CARRIERS, Neurology, 44(4), 1994, pp. 10000187-10000188
DETECTION OF NEW PATERNAL DYSTROPHIN GENE-MUTATIONS IN ISOLATED CASESOF DYSTROPHINOPATHY IN FEMALES
Authors: PEGORARO E SCHIMKE RN ARAHATA K HAYASHI Y STERN H MARKS H GLASBERG MR CARROLL JE TABER JW WESSEL HB BAUSERMAN SC MARKS WA TORIELLO HV HIGGINS JV APPLETON S SCHWARTZ L GARCIA CA HOFFMAN EP
Citation: E. Pegoraro et al., DETECTION OF NEW PATERNAL DYSTROPHIN GENE-MUTATIONS IN ISOLATED CASESOF DYSTROPHINOPATHY IN FEMALES, American journal of human genetics, 54(6), 1994, pp. 989-1003
HYPERKALEMIC PERIODIC PARALYSIS - RAPID MOLECULAR DIAGNOSIS AND RELATIONSHIP OF GENOTYPE TO PHENOTYPE IN 12 FAMILIES
Authors: FEERO WG WANG J BARANY F ZHOU J TODOROVIC SM CONWIT R GALLOWAY G HAUSMANOWAPETRUSEWICZ I FIDZIANSKA A ARAHATA K WESSEL HB WADELIUS C MARKS HG HARTLAGE P HAYAKAWA H HOFFMAN EP
Citation: Wg. Feero et al., HYPERKALEMIC PERIODIC PARALYSIS - RAPID MOLECULAR DIAGNOSIS AND RELATIONSHIP OF GENOTYPE TO PHENOTYPE IN 12 FAMILIES, Neurology, 43(4), 1993, pp. 668-673
MOLECULAR-GENETIC AND GENETIC CORRELATIONS IN SODIUM CHANNELOPATHIES - LACK OF FOUNDER EFFECT AND EVIDENCE FOR A 2ND GENE
Authors: WANG J ZHOU J TODOROVIC SM FEERO WG BARANY F CONWIT R HAUSMANOWAPETRUSEWICZ I FIDZIANSKA A ARAHATA K WESSEL HB SILLEN A MARKS HG HARTLAGE P GALLOWAY G RICKER K LEHMANNHORN F HAYAKAWA H HOFFMAN EP
Citation: J. Wang et al., MOLECULAR-GENETIC AND GENETIC CORRELATIONS IN SODIUM CHANNELOPATHIES - LACK OF FOUNDER EFFECT AND EVIDENCE FOR A 2ND GENE, American journal of human genetics, 52(6), 1993, pp. 1074-1084
Risultati: 1-8 |