J Med Genet -- Table of Contents (23 [6])

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December 1986 (Volume 23, Number 6). [Index by author]

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Articles

Editorial
Peter S Harper
J Med Genet 1986; 23: 481. doi:10.1136/jmg.23.6.481 [PDF] [Request Permissions]

Conference Report

The elusive muscular dystrophy gene. Fifth Muscular Dystrophy Group Workshop on the X chromosome and muscular dystrophies, April 1986
Kay E Davies
J Med Genet 1986; 23: 482-483. doi:10.1136/jmg.23.6.482 [PDF] [Request Permissions]

Research Article

Muscular dystrophy in girls with X;autosome translocations.
Y Boyd, V Buckle, S Holt, E Munro, D Hunter, and I Craig
J Med Genet 1986; 23: 484-490. doi:10.1136/jmg.23.6.484 [Abstract] [PDF] [Request Permissions]

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.
V M Kean, H L Macleod, M W Thompson, P N Ray, C Verellen-Dumoulin, and R G Worton
J Med Genet 1986; 23: 491-493. doi:10.1136/jmg.23.6.491 [Abstract] [PDF] [Request Permissions]

Duchenne muscular dystrophy in one of monozygotic twin girls.
J Burn, S Povey, Y Boyd, E A Munro, L West, K Harper, and D Thomas
J Med Genet 1986; 23: 494-500. doi:10.1136/jmg.23.6.494 [Abstract] [PDF] [Request Permissions]

Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies.
A Clarke, S H Roberts, N S Thomas, A Whitfield, J Williams, and P S Harper
J Med Genet 1986; 23: 501-508. doi:10.1136/jmg.23.6.501 [Abstract] [PDF] [Request Permissions]

Molecular deletion analysis in Duchenne muscular dystrophy.
N S Thomas, P N Ray, R G Worton, and P S Harper
J Med Genet 1986; 23: 509-515. doi:10.1136/jmg.23.6.509 [Abstract] [PDF] [Request Permissions]

The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.
K Hart, C Cole, A Walker, S Hodgson, L Johnson, V Dubowitz, P Ray, R Worton, and M Bobrow
J Med Genet 1986; 23: 516-520. doi:10.1136/jmg.23.6.516 [Abstract] [PDF] [Request Permissions]

The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy.
J H Edwards
J Med Genet 1986; 23: 521-530. doi:10.1136/jmg.23.6.521 [Abstract] [PDF] [Request Permissions]

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.
C J Bertelson, J A Bartley, A P Monaco, C Colletti-Feener, K Fischbeck, and L M Kunkel
J Med Genet 1986; 23: 531-537. doi:10.1136/jmg.23.6.531 [Abstract] [PDF] [Request Permissions]

Linkage studies in Duchenne and Becker muscular dystrophies.
A Walker, K Hart, C Cole, S Hodgson, L Johnson, V Dubowitz, and M Bobrow
J Med Genet 1986; 23: 538-547. doi:10.1136/jmg.23.6.538 [Abstract] [PDF] [Request Permissions]

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
M W Thompson, P N Ray, B Belfall, C Duff, C Logan, I Oss, and R G Worton
J Med Genet 1986; 23: 548-555. doi:10.1136/jmg.23.6.548 [Abstract] [PDF] [Request Permissions]

Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
J M Old and K E Davies
J Med Genet 1986; 23: 556-559. doi:10.1136/jmg.23.6.556 [Abstract] [PDF] [Request Permissions]

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
M Lindlöf, H Kääriäinen, K E Davies, and A de la Chapelle
J Med Genet 1986; 23: 560-572. doi:10.1136/jmg.23.6.560 [Abstract] [PDF] [Request Permissions]

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
E Bakker, E J Bonten, L F De Lange, H Veenema, D Majoor-Krakauer, M H Hofker, G J Van Ommen, and P L Pearson
J Med Genet 1986; 23: 573-580. doi:10.1136/jmg.23.6.573 [Abstract] [PDF] [Request Permissions]

A register based system for gene tracking in Duchenne muscular dystrophy.
A P Read, L Kerzin-Storrar, R C Mountford, R G Elles, and R Harris
J Med Genet 1986; 23: 581-586. doi:10.1136/jmg.23.6.581 [Abstract] [PDF] [Request Permissions]

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.
J R Yates, N A Affara, D M Jamieson, M A Ferguson-Smith, I Hausmanowa-Petrusewicz, J Zaremba, J Borkowska, A W Johnston, and K Kelly
J Med Genet 1986; 23: 587-590. doi:10.1136/jmg.23.6.587 [Abstract] [PDF] [Request Permissions]

X linked muscular dystrophy with contractures.
A W Johnston and E McKay
J Med Genet 1986; 23: 591-595. doi:10.1136/jmg.23.6.591 [Abstract] [PDF] [Request Permissions]

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.
N S Thomas, H Williams, L J Elsas, L C Hopkins, M Sarfarazi, and P S Harper
J Med Genet 1986; 23: 596-598. doi:10.1136/jmg.23.6.596 [Abstract] [PDF] [Request Permissions]

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	Editorial Peter S Harper J Med Genet 1986; 23: 481. doi:10.1136/jmg.23.6.481 [PDF] [Request Permissions]

	The elusive muscular dystrophy gene. Fifth Muscular Dystrophy Group Workshop on the X chromosome and muscular dystrophies, April 1986 Kay E Davies J Med Genet 1986; 23: 482-483. doi:10.1136/jmg.23.6.482 [PDF] [Request Permissions]

	Muscular dystrophy in girls with X;autosome translocations. Y Boyd, V Buckle, S Holt, E Munro, D Hunter, and I Craig J Med Genet 1986; 23: 484-490. doi:10.1136/jmg.23.6.484 [Abstract] [PDF] [Request Permissions]

	Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy. V M Kean, H L Macleod, M W Thompson, P N Ray, C Verellen-Dumoulin, and R G Worton J Med Genet 1986; 23: 491-493. doi:10.1136/jmg.23.6.491 [Abstract] [PDF] [Request Permissions]

	Duchenne muscular dystrophy in one of monozygotic twin girls. J Burn, S Povey, Y Boyd, E A Munro, L West, K Harper, and D Thomas J Med Genet 1986; 23: 494-500. doi:10.1136/jmg.23.6.494 [Abstract] [PDF] [Request Permissions]

	Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies. A Clarke, S H Roberts, N S Thomas, A Whitfield, J Williams, and P S Harper J Med Genet 1986; 23: 501-508. doi:10.1136/jmg.23.6.501 [Abstract] [PDF] [Request Permissions]

	Molecular deletion analysis in Duchenne muscular dystrophy. N S Thomas, P N Ray, R G Worton, and P S Harper J Med Genet 1986; 23: 509-515. doi:10.1136/jmg.23.6.509 [Abstract] [PDF] [Request Permissions]

	The screening of Duchenne muscular dystrophy patients for submicroscopic deletions. K Hart, C Cole, A Walker, S Hodgson, L Johnson, V Dubowitz, P Ray, R Worton, and M Bobrow J Med Genet 1986; 23: 516-520. doi:10.1136/jmg.23.6.516 [Abstract] [PDF] [Request Permissions]

	The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy. J H Edwards J Med Genet 1986; 23: 521-530. doi:10.1136/jmg.23.6.521 [Abstract] [PDF] [Request Permissions]

	Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. C J Bertelson, J A Bartley, A P Monaco, C Colletti-Feener, K Fischbeck, and L M Kunkel J Med Genet 1986; 23: 531-537. doi:10.1136/jmg.23.6.531 [Abstract] [PDF] [Request Permissions]

	Linkage studies in Duchenne and Becker muscular dystrophies. A Walker, K Hart, C Cole, S Hodgson, L Johnson, V Dubowitz, and M Bobrow J Med Genet 1986; 23: 538-547. doi:10.1136/jmg.23.6.538 [Abstract] [PDF] [Request Permissions]

	Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy. M W Thompson, P N Ray, B Belfall, C Duff, C Logan, I Oss, and R G Worton J Med Genet 1986; 23: 548-555. doi:10.1136/jmg.23.6.548 [Abstract] [PDF] [Request Permissions]

	Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis. J M Old and K E Davies J Med Genet 1986; 23: 556-559. doi:10.1136/jmg.23.6.556 [Abstract] [PDF] [Request Permissions]

	Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms. M Lindlöf, H Kääriäinen, K E Davies, and A de la Chapelle J Med Genet 1986; 23: 560-572. doi:10.1136/jmg.23.6.560 [Abstract] [PDF] [Request Permissions]

	DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure. E Bakker, E J Bonten, L F De Lange, H Veenema, D Majoor-Krakauer, M H Hofker, G J Van Ommen, and P L Pearson J Med Genet 1986; 23: 573-580. doi:10.1136/jmg.23.6.573 [Abstract] [PDF] [Request Permissions]

	A register based system for gene tracking in Duchenne muscular dystrophy. A P Read, L Kerzin-Storrar, R C Mountford, R G Elles, and R Harris J Med Genet 1986; 23: 581-586. doi:10.1136/jmg.23.6.581 [Abstract] [PDF] [Request Permissions]

	Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene. J R Yates, N A Affara, D M Jamieson, M A Ferguson-Smith, I Hausmanowa-Petrusewicz, J Zaremba, J Borkowska, A W Johnston, and K Kelly J Med Genet 1986; 23: 587-590. doi:10.1136/jmg.23.6.587 [Abstract] [PDF] [Request Permissions]

	X linked muscular dystrophy with contractures. A W Johnston and E McKay J Med Genet 1986; 23: 591-595. doi:10.1136/jmg.23.6.591 [Abstract] [PDF] [Request Permissions]

	Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome. N S Thomas, H Williams, L J Elsas, L C Hopkins, M Sarfarazi, and P S Harper J Med Genet 1986; 23: 596-598. doi:10.1136/jmg.23.6.596 [Abstract] [PDF] [Request Permissions]