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On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy

โœ Scribed by Dr. G. W. Padberg; Dr. O. F. Brouwer; Dr. R. J. W. de Keizer; G. Dijkman; Dr. C. Wijmenga; Dr. J. J. Grote; R. R. Frants

Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
835 KB
Volume
18
Category
Article
ISSN
0148-639X

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Characterization of a tandemly repeated
Characterization of a tandemly repeated 3.3-kb Kpnl unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35
โœ Dr. Je Hyeon Lee; Ms. Kanako Goto; Dr. Chie Matsuda; Dr. Kiichi Arahata ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 769 KB

A 3.3-kb Kpnl repeat unit within the tandem repeat locus (D4Z4) and its upstream 2.5-kb HinclllKpnl fragment of the facioscapulohumeral muscular dystrophy (FSHD) gene region at 4q35-qter were sequenced and characterized. The 3.3-kb Kpnl unit was 3303 bp in length and contained two homeodomain sequen