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Literature DB >> 5659903

Coats' disease and muscular dystrophy.

R G Small.

Abstract

Entities: Disease

Mesh：

Year: 1968 PMID： 5659903

Source DB: PubMed Journal: Trans Am Acad Ophthalmol Otolaryngol ISSN： 0002-7154

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11 in total

1. A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred.

Authors: F M Häfner; A A Salam; T E Linder; D Balmer; A Baumer; A A Schinzel; T Spillmann; S M Leal
Journal: Am J Hum Genet Date: 2000-03-17 Impact factor: 11.025

2. Hearing loss in facioscapulohumeral dystrophy.

Authors: T Voit; A Lamprecht; H G Lenard; H H Goebel
Journal: Eur J Pediatr Date: 1986-09 Impact factor: 3.183

3. Electron microscopical study of Coat's disease.

Authors: R Tripathi; N Ashton
Journal: Br J Ophthalmol Date: 1971-05 Impact factor: 4.638

4. Norrie's disease in North America.

Authors: F C Blodi; W S Hunter
Journal: Doc Ophthalmol Date: 1969 Impact factor: 2.379

Review 5. Advanced Coats' disease.

Authors: B G Haik
Journal: Trans Am Ophthalmol Soc Date: 1991

6. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).

Authors: P E Jardine; M C Koch; P W Lunt; J Maynard; K D Bathke; P S Harper; M Upadhyaya
Journal: Arch Dis Child Date: 1994-09 Impact factor: 3.791

7. Dominant lethal pathologies in male mice engineered to contain an X-linked DUX4 transgene.

Authors: Abhijit Dandapat; Darko Bosnakovski; Lynn M Hartweck; Robert W Arpke; Kristen A Baltgalvis; Derek Vang; June Baik; Radbod Darabi; Rita C R Perlingeiro; F Kent Hamra; Kalpna Gupta; Dawn A Lowe; Michael Kyba
Journal: Cell Rep Date: 2014-08-28 Impact factor: 9.423