Literature DB >> 5637795

Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.

C E Jackson, D A Strehler.   

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Year:  1968        PMID: 5637795

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


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  11 in total

1.  Report of ENMC workshop on the limb-girdle muscular dystrophies.

Authors:  A Clarke
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

2.  Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Authors:  M C Speer; L H Yamaoka; J H Gilchrist; C P Gaskell; J M Stajich; J M Vance; A Kazantsev; A A Lastra; C S Haynes; J S Beckmann
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

3.  Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.

Authors:  M C Speer; J M Vance; J M Grubber; F Lennon Graham; J M Stajich; K D Viles; A Rogala; R McMichael; J Chutkow; C Goldsmith; R W Tim; M A Pericak-Vance
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

4.  DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.

Authors:  V M Pratt; C E Jackson; D C Wallace; D S Gurley; A Feit; G L Feldman
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

5.  Fortuitous detection of a sporadic carrier of Duchenne's muscular dystrophy.

Authors:  J W Hanson; H Zellweger; A K Afifi; W F McCormick
Journal:  Humangenetik       Date:  1968

6.  Consanguinity and blood group distribution in an Amish Isolate.

Authors:  C E Jackson; W E Symon; E L Pruden; I M Kaehr; J D Mann
Journal:  Am J Hum Genet       Date:  1968-11       Impact factor: 11.025

7.  Amish albinism: a distinctive autosomal recessive phenotype.

Authors:  W E Nance; C E Jackson; C J Witkop
Journal:  Am J Hum Genet       Date:  1970-09       Impact factor: 11.025

8.  Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.

Authors:  V Allamand; O Broux; I Richard; F Fougerousse; N Chiannilkulchai; N Bourg; L Brenguier; C Devaud; P Pasturaud; A Pereira de Souza
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

9.  Limb girdle muscular dystrophy: a radiologic and manometric study of the pharynx and esophagus.

Authors:  J P Stübgen
Journal:  Dysphagia       Date:  1996       Impact factor: 3.438

10.  Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.

Authors:  M C Speer; J M Gilchrist; J G Chutkow; R McMichael; C A Westbrook; J M Stajich; E M Jorgenson; P C Gaskell; B L Rosi; R Ramesar
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

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