J Med Genet -- Table of Contents (26 [4])

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April 1989 (Volume 26, Number 4). [Index by author]

		Abstracts of the Meeting of the Association of Clinical Cytogeneticists Held on 5 to 7 July 1988 in Edinburgh Research Article

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Abstracts of the Meeting of the Association of Clinical Cytogeneticists Held on 5 to 7 July 1988 in Edinburgh

Abstracts of the meeting of the Association of Clinical Cytogeneticists held on 5 to 7 July 1988 in Edinburgh
J Med Genet 1989; 26: 282-286. doi:10.1136/jmg.26.4.282 [PDF] [Request Permissions]

Research Article

Molecular genetics as a diagnostic service.
P S Harper
J Med Genet 1989; 26: 217-218. doi:10.1136/jmg.26.4.217 [PDF] [Request Permissions]

Molecular genetics in the National Health Service in Britain.
R Harris, R Elles, D Craufurd, A Dodge, A Ivinson, K Hodgkinson, R Mountford, M Schwartz, T Strachan, and A Read
J Med Genet 1989; 26: 219-225. doi:10.1136/jmg.26.4.219 [Abstract] [PDF] [Request Permissions]

Demand for DNA probe testing in three genetic centres in Britain (August 1986 to July 1987).
R J Rona, A V Swan, R Beech, L Prentice, A Reynolds, O Wilson, G Mole, and P Vadera
J Med Genet 1989; 26: 226-236. doi:10.1136/jmg.26.4.226 [Abstract] [PDF] [Request Permissions]

Genetic services in the context of DNA probes: what do they cost?
R Beech, R J Rona, A V Swan, F B Kavanagh, L Prentice, O M Wilson, G Mole, and P Vadera
J Med Genet 1989; 26: 237-244. doi:10.1136/jmg.26.4.237 [Abstract] [PDF] [Request Permissions]

Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA banking.
J R Yates, S Malcolm, and A P Read
J Med Genet 1989; 26: 245-250. doi:10.1136/jmg.26.4.245 [PDF] [Request Permissions]

Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.
G K Suthers, J I Manson, L M Stern, E A Haan, and J C Mulley
J Med Genet 1989; 26: 251-254. doi:10.1136/jmg.26.4.251 [Abstract] [PDF] [Request Permissions]

Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.
M J Kotze, E Langenhoven, A E Retief, H C Seftel, H E Henderson, and H F Weich
J Med Genet 1989; 26: 255-259. doi:10.1136/jmg.26.4.255 [Abstract] [PDF] [Request Permissions]

The recurrence risks for mild idiopathic mental retardation.
S Bundey, A Thake, and J Todd
J Med Genet 1989; 26: 260-266. doi:10.1136/jmg.26.4.260 [Abstract] [PDF] [Request Permissions]

Consanguinity related prenatal and postnatal mortality of the populations of seven Pakistani Punjab cities.
S A Shami, L H Schmitt, and A H Bittles
J Med Genet 1989; 26: 267-271. doi:10.1136/jmg.26.4.267 [Abstract] [PDF] [Request Permissions]

Congenital central hypoventilation syndrome and Hirschsprung's disease in half sibs.
J Hamilton and J N Bodurtha
J Med Genet 1989; 26: 272-274. doi:10.1136/jmg.26.4.272 [Abstract] [PDF] [Request Permissions]

Holoprosencephaly: variation of expression in face and brain in three sibs.
C P Zwetsloot, O F Brouwer, and P D Maaswinkel-Mooy
J Med Genet 1989; 26: 274-276. doi:10.1136/jmg.26.4.274 [Abstract] [PDF] [Request Permissions]

Thanatophoric dysplasia in identical twins.
I D Young, I Patel, and A C Lamont
J Med Genet 1989; 26: 276-279. doi:10.1136/jmg.26.4.276 [Abstract] [PDF] [Request Permissions]

Gastrointestinal abnormalities in the syndrome of mosaic trisomy 9.
I Levy, Y Levy, Z Mammon, M Nitzan, and R Steinherz
J Med Genet 1989; 26: 280-281. doi:10.1136/jmg.26.4.280 [PDF] [Request Permissions]

Hirschsprung's disease, distinctive facies, and microcephaly.
A Bankier
J Med Genet 1989; 26: 287-288. doi:10.1136/jmg.26.4.287 [PDF] [Request Permissions]

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	Molecular genetics as a diagnostic service. P S Harper J Med Genet 1989; 26: 217-218. doi:10.1136/jmg.26.4.217 [PDF] [Request Permissions]

	Molecular genetics in the National Health Service in Britain. R Harris, R Elles, D Craufurd, A Dodge, A Ivinson, K Hodgkinson, R Mountford, M Schwartz, T Strachan, and A Read J Med Genet 1989; 26: 219-225. doi:10.1136/jmg.26.4.219 [Abstract] [PDF] [Request Permissions]

	Demand for DNA probe testing in three genetic centres in Britain (August 1986 to July 1987). R J Rona, A V Swan, R Beech, L Prentice, A Reynolds, O Wilson, G Mole, and P Vadera J Med Genet 1989; 26: 226-236. doi:10.1136/jmg.26.4.226 [Abstract] [PDF] [Request Permissions]

	Genetic services in the context of DNA probes: what do they cost? R Beech, R J Rona, A V Swan, F B Kavanagh, L Prentice, O M Wilson, G Mole, and P Vadera J Med Genet 1989; 26: 237-244. doi:10.1136/jmg.26.4.237 [Abstract] [PDF] [Request Permissions]

	Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA banking. J R Yates, S Malcolm, and A P Read J Med Genet 1989; 26: 245-250. doi:10.1136/jmg.26.4.245 [PDF] [Request Permissions]

	Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree. G K Suthers, J I Manson, L M Stern, E A Haan, and J C Mulley J Med Genet 1989; 26: 251-254. doi:10.1136/jmg.26.4.251 [Abstract] [PDF] [Request Permissions]

	Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus. M J Kotze, E Langenhoven, A E Retief, H C Seftel, H E Henderson, and H F Weich J Med Genet 1989; 26: 255-259. doi:10.1136/jmg.26.4.255 [Abstract] [PDF] [Request Permissions]

	The recurrence risks for mild idiopathic mental retardation. S Bundey, A Thake, and J Todd J Med Genet 1989; 26: 260-266. doi:10.1136/jmg.26.4.260 [Abstract] [PDF] [Request Permissions]

	Consanguinity related prenatal and postnatal mortality of the populations of seven Pakistani Punjab cities. S A Shami, L H Schmitt, and A H Bittles J Med Genet 1989; 26: 267-271. doi:10.1136/jmg.26.4.267 [Abstract] [PDF] [Request Permissions]

	Congenital central hypoventilation syndrome and Hirschsprung's disease in half sibs. J Hamilton and J N Bodurtha J Med Genet 1989; 26: 272-274. doi:10.1136/jmg.26.4.272 [Abstract] [PDF] [Request Permissions]

	Holoprosencephaly: variation of expression in face and brain in three sibs. C P Zwetsloot, O F Brouwer, and P D Maaswinkel-Mooy J Med Genet 1989; 26: 274-276. doi:10.1136/jmg.26.4.274 [Abstract] [PDF] [Request Permissions]

	Thanatophoric dysplasia in identical twins. I D Young, I Patel, and A C Lamont J Med Genet 1989; 26: 276-279. doi:10.1136/jmg.26.4.276 [Abstract] [PDF] [Request Permissions]

	Gastrointestinal abnormalities in the syndrome of mosaic trisomy 9. I Levy, Y Levy, Z Mammon, M Nitzan, and R Steinherz J Med Genet 1989; 26: 280-281. doi:10.1136/jmg.26.4.280 [PDF] [Request Permissions]

	Hirschsprung's disease, distinctive facies, and microcephaly. A Bankier J Med Genet 1989; 26: 287-288. doi:10.1136/jmg.26.4.287 [PDF] [Request Permissions]