J Med Genet -- Table of Contents (26 [11])

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November 1989 (Volume 26, Number 11). [Index by author]

		Correspondence Conference Report Research Article

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Correspondence

Correspondence
I D Young and A C Lamont
J Med Genet 1989; 26: 735-736. doi:10.1136/jmg.26.11.735-a [PDF] [Request Permissions]

Conference Report

The Association of Physicians of Great Britain and Northern Ireland, Oxford, 14 to 15 April 1989
P W Lunt
J Med Genet 1989; 26: 733-734. doi:10.1136/jmg.26.11.733 [PDF] [Request Permissions]

Research Article

Linkage disequilibrium in Huntington's disease: an improved localisation for the gene.
R G Snell, L P Lazarou, S Youngman, O W Quarrell, J J Wasmuth, D J Shaw, and P S Harper
J Med Genet 1989; 26: 673-675. doi:10.1136/jmg.26.11.673 [Abstract] [PDF] [Request Permissions]

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene.
J Theilmann, S Kanani, R Shiang, C Robbins, O Quarrell, M Huggins, A Hedrick, B Weber, C Collins, and J J Wasmuth
J Med Genet 1989; 26: 676-681. doi:10.1136/jmg.26.11.676 [Abstract] [PDF] [Request Permissions]

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.
S Hodgson, K Hart, S Abbs, J Heckmatt, E Rodillo, M Bobrow, and V Dubowitz
J Med Genet 1989; 26: 682-693. doi:10.1136/jmg.26.11.682 [Abstract] [PDF] [Request Permissions]

Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis.
L I al-Gazali, R J Arthur, J T Lamb, H M Hammer, T P Coker, P N Hirschmann, J Gibbs, and R F Mueller
J Med Genet 1989; 26: 694-703. doi:10.1136/jmg.26.11.694 [Abstract] [PDF] [Request Permissions]

A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.
S M Huson, D A Compston, P Clark, and P S Harper
J Med Genet 1989; 26: 704-711. doi:10.1136/jmg.26.11.704 [Abstract] [PDF] [Request Permissions]

A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.
S M Huson, D A Compston, and P S Harper
J Med Genet 1989; 26: 712-721. doi:10.1136/jmg.26.11.712 [Abstract] [PDF] [Request Permissions]

Fountain's syndrome: mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips.
J P Fryns
J Med Genet 1989; 26: 722-724. doi:10.1136/jmg.26.11.722 [PDF] [Request Permissions]

Abnormal chromosome complement resulting from a familial inversion of chromosome 2.
S Richter, B Lockwood, D Lockwood, and J Allanson
J Med Genet 1989; 26: 725-729. doi:10.1136/jmg.26.11.725 [Abstract] [PDF] [Request Permissions]

Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features.
L A Brueton, J C Barber, S M Huson, and R M Winter
J Med Genet 1989; 26: 729-730. doi:10.1136/jmg.26.11.729 [Abstract] [PDF] [Request Permissions]

Pituitary function studies in a case of mild Hunter's syndrome (MPS IIB).
J Nelson and D Carson
J Med Genet 1989; 26: 731-732. doi:10.1136/jmg.26.11.731 [Abstract] [PDF] [Request Permissions]

Thanatophoric dysplasia in identical twins.
A S Knisely
J Med Genet 1989; 26: 735-736. doi:10.1136/jmg.26.11.735 [PDF] [Request Permissions]

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	Correspondence I D Young and A C Lamont J Med Genet 1989; 26: 735-736. doi:10.1136/jmg.26.11.735-a [PDF] [Request Permissions]

	The Association of Physicians of Great Britain and Northern Ireland, Oxford, 14 to 15 April 1989 P W Lunt J Med Genet 1989; 26: 733-734. doi:10.1136/jmg.26.11.733 [PDF] [Request Permissions]

	Linkage disequilibrium in Huntington's disease: an improved localisation for the gene. R G Snell, L P Lazarou, S Youngman, O W Quarrell, J J Wasmuth, D J Shaw, and P S Harper J Med Genet 1989; 26: 673-675. doi:10.1136/jmg.26.11.673 [Abstract] [PDF] [Request Permissions]

	Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene. J Theilmann, S Kanani, R Shiang, C Robbins, O Quarrell, M Huggins, A Hedrick, B Weber, C Collins, and J J Wasmuth J Med Genet 1989; 26: 676-681. doi:10.1136/jmg.26.11.676 [Abstract] [PDF] [Request Permissions]

	Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. S Hodgson, K Hart, S Abbs, J Heckmatt, E Rodillo, M Bobrow, and V Dubowitz J Med Genet 1989; 26: 682-693. doi:10.1136/jmg.26.11.682 [Abstract] [PDF] [Request Permissions]

	Diagnostic and counselling difficulties using a fully comprehensive screening protocol for families at risk for tuberous sclerosis. L I al-Gazali, R J Arthur, J T Lamb, H M Hammer, T P Coker, P N Hirschmann, J Gibbs, and R F Mueller J Med Genet 1989; 26: 694-703. doi:10.1136/jmg.26.11.694 [Abstract] [PDF] [Request Permissions]

	A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity. S M Huson, D A Compston, P Clark, and P S Harper J Med Genet 1989; 26: 704-711. doi:10.1136/jmg.26.11.704 [Abstract] [PDF] [Request Permissions]

	A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling. S M Huson, D A Compston, and P S Harper J Med Genet 1989; 26: 712-721. doi:10.1136/jmg.26.11.712 [Abstract] [PDF] [Request Permissions]

	Fountain's syndrome: mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips. J P Fryns J Med Genet 1989; 26: 722-724. doi:10.1136/jmg.26.11.722 [PDF] [Request Permissions]

	Abnormal chromosome complement resulting from a familial inversion of chromosome 2. S Richter, B Lockwood, D Lockwood, and J Allanson J Med Genet 1989; 26: 725-729. doi:10.1136/jmg.26.11.725 [Abstract] [PDF] [Request Permissions]

	Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features. L A Brueton, J C Barber, S M Huson, and R M Winter J Med Genet 1989; 26: 729-730. doi:10.1136/jmg.26.11.729 [Abstract] [PDF] [Request Permissions]

	Pituitary function studies in a case of mild Hunter's syndrome (MPS IIB). J Nelson and D Carson J Med Genet 1989; 26: 731-732. doi:10.1136/jmg.26.11.731 [Abstract] [PDF] [Request Permissions]

	Thanatophoric dysplasia in identical twins. A S Knisely J Med Genet 1989; 26: 735-736. doi:10.1136/jmg.26.11.735 [PDF] [Request Permissions]

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