Literature DB >> 5780363

Genetic studies of a family with two unusual autosomal dominant conditions: muscular dystrophy and Pelger-Huet anomaly. Clinical, pathologic and linkage considerations.

L J Schneiderman, W I Sampson, W C Schoene, G B Haydon.   

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Year:  1969        PMID: 5780363     DOI: 10.1016/0002-9343(69)90040-0

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


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  5 in total

1.  Severe generalized muscular atrophia, nerve optic atrophia, ear problem and disability with Pelger-Huet anomaly.

Authors:  Hassan Mahmoodi Nesheli; Naimeh Nakhjavani; Tahere Galini Moghaddam
Journal:  Caspian J Intern Med       Date:  2011

2.  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

Review 3.  [New data on the genetics and classification of muscular dystrophies].

Authors:  P E Becker
Journal:  Humangenetik       Date:  1972

4.  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

Review 5.  DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies.

Authors:  Alessandra Ruggieri; Simona Saredi; Simona Zanotti; Maria Barbara Pasanisi; Lorenzo Maggi; Marina Mora
Journal:  Front Mol Biosci       Date:  2016-09-30
  5 in total

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