Literature DB >> 2570156

A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes.

M Upadhyaya1, M Sarfarazi, P W Lunt, W Broadhead, P S Harper.   

Abstract

From analysis of DNA polymorphisms in a panel of 455 subjects from 25 families with facioscapulohumeral (Landouzy-Déjérine) disease, we have found no evidence for close linkage of the disease at 24 different genetic loci, including one from a candidate chromosomal region. Added to previous data, our results provide direction for future collaborative linkage studies.

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Year:  1989        PMID： 2570156      PMCID： PMC1015669          DOI： 10.1136/jmg.26.8.490

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  10 in total

1.  Discrimination of genetic entities in muscular dystrophy.

Authors:  C S CHUNG; N E MORTON
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

2.  A pedigree of hereditary progressive muscular dystrophy.

Authors:  J W BOYES; F C FRASER
Journal:  Ann Eugen       Date:  1949-10

Review 3.  A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988.

Authors:  P W Lunt
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

4.  An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Authors:  M Sarfarazi; M Upadhyaya; G Padberg; M Pericak-Vance; T Siddique; G Lucotte; P Lunt
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

5.  Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14.

Authors:  P W Lunt; J G Noades; M Upadhyaya; M Sarfarazi; P S Harper
Journal:  J Neurol Sci       Date:  1988-12       Impact factor: 3.181

6.  Linkage studies in facioscapulohumeral muscular dystrophy.

Authors:  G W Padberg; E C Klasen; W S Volkers; G G De Lange; A R Wintzen
Journal:  Muscle Nerve       Date:  1988-08       Impact factor: 3.217

7.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

8.  Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophy.

Authors:  G Padberg; A W Eriksson; W S Volkers; L Bernini; E Van Loghem; P Meera Khan; L E Nijenhuis; J C Pronk; G M Schreuder
Journal:  J Neurol Sci       Date:  1984-09       Impact factor: 3.181

9.  Localization of the gene for familial adenomatous polyposis on chromosome 5.

Authors:  W F Bodmer; C J Bailey; J Bodmer; H J Bussey; A Ellis; P Gorman; F C Lucibello; V A Murday; S H Rider; P Scambler
Journal:  Nature       Date:  1987 Aug 13-19       Impact factor: 49.962

Review 10.  Modern methods of diagnosis of muscle diseases.

Authors:  R H Edwards; R D Griffiths; M Hayward; T Helliwell
Journal:  J R Coll Physicians Lond       Date:  1986-01
  10 in total
  6 in total

1.  The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).

Authors:  M Upadhyaya; P Lunt; M Sarfarazi; W Broadhead; J Farnham; P S Harper
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

2.  Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Authors:  K D Mathews; K A Mills; E P Bosch; V V Ionasescu; K R Wiles; K H Buetow; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

3.  A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

Authors:  M Upadhyaya; P W Lunt; M Sarfarazi; W Broadhead; J Daniels; M Owen; P S Harper
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

4.  Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

Authors:  D M Slipetz; J R Aprille; P R Goodyer; R Rozen
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

5.  A clinically homogeneous group of families with facioscapulohumeral (Landouzy-Déjérine) muscular dystrophy: linkage analysis of six autosomes.

Authors:  S J Jacobsen; E S Diala; B V Dorsey; M B Rising; R Graveline; K Falls; P Schultz; C Hogan; K Rediker; C D'Amico
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

6.  An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Authors:  M Sarfarazi; M Upadhyaya; G Padberg; M Pericak-Vance; T Siddique; G Lucotte; P Lunt
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318
  6 in total

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