108 related articles for article (PubMed ID: 3398874)
1. Becker muscular dystrophy recombinant DNA studies in identical twins.
Ionasescu V; Ionasescu R; Searby C; Burns T
Muscle Nerve; 1988 Apr; 11(4):287-90. PubMed ID: 3398874
[TBL] [Abstract][Full Text] [Related]
2. Duchenne muscular dystrophy in monozygotic twins: deletion of 5' fragments of the gene.
Ionasescu VV; Searby CC; Ionasescu R; Patil S
Am J Med Genet; 1989 May; 33(1):113-6. PubMed ID: 2750778
[TBL] [Abstract][Full Text] [Related]
3. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
Lupski JR; Garcia CA; Zoghbi HY; Hoffman EP; Fenwick RG
Am J Med Genet; 1991 Sep; 40(3):354-64. PubMed ID: 1683155
[TBL] [Abstract][Full Text] [Related]
4. [Spinal form of Ullrich's disease in monozygotic twins].
Aver'ianov IuN; Il'ina NA; Mazaeva IV; Berezova NIu
Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):51-4. PubMed ID: 7200707
[TBL] [Abstract][Full Text] [Related]
5. Emery-Dreifuss muscular dystrophy with unusual features.
Deymeer F; Oge AE; Bayindir C; Kaymaz C; Nişanci Y; Adalet K; Yates JR; Ozdemir C
Muscle Nerve; 1993 Dec; 16(12):1359-65. PubMed ID: 8232393
[TBL] [Abstract][Full Text] [Related]
6. Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.
Abbadi N; Philippe C; Chery M; Gilgenkrantz H; Tome F; Collin H; Theau D; Recan D; Broux O; Fardeau M
Am J Med Genet; 1994 Aug; 52(2):198-206. PubMed ID: 7802009
[TBL] [Abstract][Full Text] [Related]
7. Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins.
Gomez MR; Engel AG; Dewald G; Peterson HA
Neurology; 1977 Jun; 27(6):537-41. PubMed ID: 559260
[TBL] [Abstract][Full Text] [Related]
8. [Pseudohypertrophic forms of progressive muscular dystrophy with the onset at puberty and a malignant course of the myodystrophic process].
Badalian LO; Arkhipov BA; Temin PA; Zavadenko NN; Voloshina TG
Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(3):61-4. PubMed ID: 3381616
[TBL] [Abstract][Full Text] [Related]
9. Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy.
Chutkow JG; Hyser CL; Edwards JA; Heffner RR; Czyrny JJ
Neurology; 1987 Jul; 37(7):1147-51. PubMed ID: 2885783
[TBL] [Abstract][Full Text] [Related]
10. Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies.
Ionasescu VV; Searby CC; Ionasescu R
Acta Neurol Scand; 1989 Jun; 79(6):500-3. PubMed ID: 2782030
[TBL] [Abstract][Full Text] [Related]
11. Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy.
Tawil R; Storvick D; Weiffenbach B; Altherr MR; Feasby TE; Griggs RC
Hum Mutat; 1993; 2(6):492-4. PubMed ID: 8111417
[No Abstract] [Full Text] [Related]
12. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
Wilton SD; Chandler DC; Kakulas BA; Laing NG
Hum Mutat; 1994; 3(2):133-40. PubMed ID: 8199594
[TBL] [Abstract][Full Text] [Related]
13. Treatment of Duchenne muscular dystrophy with growth hormone inhibitors.
Zatz M; Betti RT; Frota-Pessoa O
Am J Med Genet; 1986 Jul; 24(3):549-66. PubMed ID: 3524231
[TBL] [Abstract][Full Text] [Related]
14. [HLA and familial multiple sclerosis].
Barroche G; Perrier P; Raffoux C; Gehin P; Streiff F; Weber M
Rev Neurol (Paris); 1986; 142(10):738-45. PubMed ID: 3823705
[TBL] [Abstract][Full Text] [Related]
15. [Association of sporadic limb-girdle muscular dystrophy and autonomous thyroid nodule in 3 Germans].
Di Lorenzo L; Lupoli G; Cosentini E; Rippa PG; Lombardi G
Minerva Endocrinol; 1991; 16(3):147-51. PubMed ID: 1806812
[TBL] [Abstract][Full Text] [Related]
16. [Monozygotic twins with progressive muscular dystrophy].
Radu H; Killyen I; Rosu AM; Ionescu V
Z Neurol; 1972; 202(3):241-6. PubMed ID: 4120053
[No Abstract] [Full Text] [Related]
17. In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy.
Zneimer SM; Schneider NR; Richards CS
Am J Med Genet; 1993 Mar; 45(5):601-5. PubMed ID: 8456832
[TBL] [Abstract][Full Text] [Related]
18. [Muscular dystrophy of the Becker type].
Carbajal-Rodríguez L; de Quevedo JJ; Loredo-Abdalá A; Villaseñor-Zepeda J
Bol Med Hosp Infant Mex; 1988 Sep; 45(9):605-9. PubMed ID: 3190853
[No Abstract] [Full Text] [Related]
19. Becker muscular dystrophy.
Fu HD; Tang XF; Guo YP
Chin Med J (Engl); 1989 May; 102(5):373-7. PubMed ID: 2509161
[TBL] [Abstract][Full Text] [Related]
20. Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families.
Arenas D; Coral R; Cisneros B; Peñaloza L; Salamanca F; Kofman S; Mercado R; Méndez J; Martínez C; Montañez C
Arch Med Res; 1996; 27(2):151-6. PubMed ID: 8696057
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
