J Med Genet -- Table of Contents (25 [9])

Home > Volume 25, Number 9

Only Abstracts and PDFs available for this issue

Other Issues:
September 1988 (Volume 25, Number 9). [Index by author]

		Articles Miscellaneous Articles Book Reviews Research Article

Find articles in this issue containing these words: [Search ALL Issues]

Table of Contents (PDF) | Cover (PDF) | Administration (PDF)

To see an article, click its [Full Text] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstracts' button. To see one abstract at a time, click its [Abstract] link.

Articles

Abstracts of the meeting of the Clinical Genetics Society held on 7 and 8 April 1988 at the University of Oxford
J Med Genet 1988; 25: 638-646. doi:10.1136/jmg.25.9.638 [PDF] [Request Permissions]

Miscellaneous

Correction
J Med Genet 1988; 25: 646. doi:10.1136/jmg.25.9.646 [PDF] [Request Permissions]

Book Reviews

Oncology and Immunology of Down Syndrome
Alan E H Emery
J Med Genet 1988; 25: 647. doi:10.1136/jmg.25.9.647 [PDF] [Request Permissions]

Genetic Risk, Risk Perception, and Decision Making
L Kerzin-Storrar
J Med Genet 1988; 25: 647-648. doi:10.1136/jmg.25.9.647-a [PDF] [Request Permissions]

Cystic Fibrosis: The Facts
M Goodchild
J Med Genet 1988; 25: 648. doi:10.1136/jmg.25.9.648 [PDF] [Request Permissions]

Genetics and Malformations in Art
Alan E H Emery
J Med Genet 1988; 25: 648. doi:10.1136/jmg.25.9.648-a [PDF] [Request Permissions]

Research Article

Considerations in using linkage analysis as a presymptomatic test for Huntington's disease.
L A Farrer, R H Myers, L A Cupples, and P M Conneally
J Med Genet 1988; 25: 577-588. doi:10.1136/jmg.25.9.577 [Abstract] [PDF] [Request Permissions]

Anticipation in Huntington's disease is inherited through the male line but may originate in the female.
R M Ridley, C D Frith, T J Crow, and P M Conneally
J Med Genet 1988; 25: 589-595. doi:10.1136/jmg.25.9.589 [Abstract] [PDF] [Request Permissions]

Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.
G Rumsby, A H Fielder, W M Hague, and J W Honour
J Med Genet 1988; 25: 596-599. doi:10.1136/jmg.25.9.596 [Abstract] [PDF] [Request Permissions]

Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy.
J Poulton, D M Turnbull, A B Mehta, J Wilson, and R M Gardiner
J Med Genet 1988; 25: 600-605. doi:10.1136/jmg.25.9.600 [Abstract] [PDF] [Request Permissions]

Prospective prenatal screening for fetal abnormalities using a quantitative immunoassay for acetylcholinesterase.
D J Brock and L Barron
J Med Genet 1988; 25: 606-608. doi:10.1136/jmg.25.9.606 [Abstract] [PDF] [Request Permissions]

Sequential sampling in clinical cytogenetics: a quality control viewpoint.
M A De Arce and S P McManus
J Med Genet 1988; 25: 609-618. doi:10.1136/jmg.25.9.609 [Abstract] [PDF] [Request Permissions]

A probably distinct autosomal recessive thoraco-limb dysplasia.
H Rivera, J M Perez-Salas, Z Nazara, and M L Ramirez
J Med Genet 1988; 25: 619-622. doi:10.1136/jmg.25.9.619 [Abstract] [PDF] [Request Permissions]

Alport's syndrome.
M A Crawfurd
J Med Genet 1988; 25: 623-627. doi:10.1136/jmg.25.9.623 [PDF] [Request Permissions]

Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment.
T Motegi, K Nakamura, T Terakawa, A Oohira, K Minoda, K Kishi, Y Yanagawa, and H Hayakawa
J Med Genet 1988; 25: 628-630. doi:10.1136/jmg.25.9.628 [Abstract] [PDF] [Request Permissions]

Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents.
R L Neu, B G Kousseff, D E Hardy, Y P Essig, K L Miller, G A Jervis, and T A Tedesco
J Med Genet 1988; 25: 631-633. doi:10.1136/jmg.25.9.631 [Abstract] [PDF] [Request Permissions]

Linkage analysis of manic depression in an Irish family using H-ras 1 and INS DNA markers.
M Gill, P McKeon, and P Humphries
J Med Genet 1988; 25: 634-635. doi:10.1136/jmg.25.9.634 [PDF] [Request Permissions]

Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line.
M G Wilson and M S Lin
J Med Genet 1988; 25: 635-636. doi:10.1136/jmg.25.9.635 [PDF] [Request Permissions]

A new centromeric heteromorphism in the short arm of chromosome 20.
J P Fryns, A Kleczkowska, E Smeets, and H van den Berghe
J Med Genet 1988; 25: 636-637. doi:10.1136/jmg.25.9.636 [PDF] [Request Permissions]

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

	Abstracts of the meeting of the Clinical Genetics Society held on 7 and 8 April 1988 at the University of Oxford J Med Genet 1988; 25: 638-646. doi:10.1136/jmg.25.9.638 [PDF] [Request Permissions]

	Correction J Med Genet 1988; 25: 646. doi:10.1136/jmg.25.9.646 [PDF] [Request Permissions]

	Oncology and Immunology of Down Syndrome Alan E H Emery J Med Genet 1988; 25: 647. doi:10.1136/jmg.25.9.647 [PDF] [Request Permissions]

	Genetic Risk, Risk Perception, and Decision Making L Kerzin-Storrar J Med Genet 1988; 25: 647-648. doi:10.1136/jmg.25.9.647-a [PDF] [Request Permissions]

	Cystic Fibrosis: The Facts M Goodchild J Med Genet 1988; 25: 648. doi:10.1136/jmg.25.9.648 [PDF] [Request Permissions]

	Genetics and Malformations in Art Alan E H Emery J Med Genet 1988; 25: 648. doi:10.1136/jmg.25.9.648-a [PDF] [Request Permissions]

	Considerations in using linkage analysis as a presymptomatic test for Huntington's disease. L A Farrer, R H Myers, L A Cupples, and P M Conneally J Med Genet 1988; 25: 577-588. doi:10.1136/jmg.25.9.577 [Abstract] [PDF] [Request Permissions]

	Anticipation in Huntington's disease is inherited through the male line but may originate in the female. R M Ridley, C D Frith, T J Crow, and P M Conneally J Med Genet 1988; 25: 589-595. doi:10.1136/jmg.25.9.589 [Abstract] [PDF] [Request Permissions]

	Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency. G Rumsby, A H Fielder, W M Hague, and J W Honour J Med Genet 1988; 25: 596-599. doi:10.1136/jmg.25.9.596 [Abstract] [PDF] [Request Permissions]

	Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy. J Poulton, D M Turnbull, A B Mehta, J Wilson, and R M Gardiner J Med Genet 1988; 25: 600-605. doi:10.1136/jmg.25.9.600 [Abstract] [PDF] [Request Permissions]

	Prospective prenatal screening for fetal abnormalities using a quantitative immunoassay for acetylcholinesterase. D J Brock and L Barron J Med Genet 1988; 25: 606-608. doi:10.1136/jmg.25.9.606 [Abstract] [PDF] [Request Permissions]

	Sequential sampling in clinical cytogenetics: a quality control viewpoint. M A De Arce and S P McManus J Med Genet 1988; 25: 609-618. doi:10.1136/jmg.25.9.609 [Abstract] [PDF] [Request Permissions]

	A probably distinct autosomal recessive thoraco-limb dysplasia. H Rivera, J M Perez-Salas, Z Nazara, and M L Ramirez J Med Genet 1988; 25: 619-622. doi:10.1136/jmg.25.9.619 [Abstract] [PDF] [Request Permissions]

	Alport's syndrome. M A Crawfurd J Med Genet 1988; 25: 623-627. doi:10.1136/jmg.25.9.623 [PDF] [Request Permissions]

	Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment. T Motegi, K Nakamura, T Terakawa, A Oohira, K Minoda, K Kishi, Y Yanagawa, and H Hayakawa J Med Genet 1988; 25: 628-630. doi:10.1136/jmg.25.9.628 [Abstract] [PDF] [Request Permissions]

	Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents. R L Neu, B G Kousseff, D E Hardy, Y P Essig, K L Miller, G A Jervis, and T A Tedesco J Med Genet 1988; 25: 631-633. doi:10.1136/jmg.25.9.631 [Abstract] [PDF] [Request Permissions]

	Linkage analysis of manic depression in an Irish family using H-ras 1 and INS DNA markers. M Gill, P McKeon, and P Humphries J Med Genet 1988; 25: 634-635. doi:10.1136/jmg.25.9.634 [PDF] [Request Permissions]

	Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line. M G Wilson and M S Lin J Med Genet 1988; 25: 635-636. doi:10.1136/jmg.25.9.635 [PDF] [Request Permissions]

	A new centromeric heteromorphism in the short arm of chromosome 20. J P Fryns, A Kleczkowska, E Smeets, and H van den Berghe J Med Genet 1988; 25: 636-637. doi:10.1136/jmg.25.9.636 [PDF] [Request Permissions]

Register for free content

Genetics jobs