Report of the UKEMS Sub-Committee on Guidelines for Mutagenicity Testing
Ilse-Dore Adler
J Med Genet 1985; 22: 496. doi:10.1136/jmg.22.6.496
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Monoclonal Antibodies and Functional Cell Lines. Progress and Applications
Alan M McGregor
J Med Genet 1985; 22: 496-497. doi:10.1136/jmg.22.6.496-a
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The Laboratory Diagnosis of Selected Inborn Errors of Metabolism
J B Holton
J Med Genet 1985; 22: 497. doi:10.1136/jmg.22.6.497
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Immunogenetics. Its Application to Clinical Medicine
N Matthews
J Med Genet 1985; 22: 497-498. doi:10.1136/jmg.22.6.497-a
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The Harvey Lectures Series 78 (1982-1983)
Andrew P Read
J Med Genet 1985; 22: 498. doi:10.1136/jmg.22.6.498
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Genetics and Neurology
A E Harding
J Med Genet 1985; 22: 498-499. doi:10.1136/jmg.22.6.498-a
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Biofuture. Confronting the Genetic Era
I D Young
J Med Genet 1985; 22: 499. doi:10.1136/jmg.22.6.499
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Black Caribs. A Case Study in Biocultural Adaptation
D F Roberts
J Med Genet 1985; 22: 499-500. doi:10.1136/jmg.22.6.499-a
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Perinatal Epidemiology
Robert G Newcombe
J Med Genet 1985; 22: 500-501. doi:10.1136/jmg.22.6.500
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Laboratory Animal Medicine
D B Morton
J Med Genet 1985; 22: 501. doi:10.1136/jmg.22.6.501
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Brave New People
I D Young
J Med Genet 1985; 22: 502. doi:10.1136/jmg.22.6.502
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Issues and Reviews in Teratology
Felix Beck
J Med Genet 1985; 22: 502. doi:10.1136/jmg.22.6.502-a
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Plasmid Technology
Duncan Shaw
J Med Genet 1985; 22: 502-503. doi:10.1136/jmg.22.6.502-b
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The Biology of Idiotypes
P N Goodfellow
J Med Genet 1985; 22: 503. doi:10.1136/jmg.22.6.503
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Ectodermal dysplasias: a clinical and genetic study
John Burn
J Med Genet 1985; 22: 503-504. doi:10.1136/jmg.22.6.503-a
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Prenatal diagnosis of the common haemoglobin disorders.
D J Weatherall, J M Old, S L Thein, J S Wainscoat, and J B Clegg
J Med Genet 1985; 22: 422-430. doi:10.1136/jmg.22.6.422
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Marcella O'Grady Boveri (1865-1950) and the chromosome theory of cancer.
V A McKusick
J Med Genet 1985; 22: 431-440. doi:10.1136/jmg.22.6.431
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Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland.
J M Connor, A F Pettigrew, I M Hann, C D Forbes, G D Lowe, and N A Affara
J Med Genet 1985; 22: 441-446. doi:10.1136/jmg.22.6.441
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Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.
P S Harper, S Youngman, M A Anderson, M Sarfarazi, O Quarrell, R Tanzi, D Shaw, P Wallace, P M Conneally, and J F Gusella
J Med Genet 1985; 22: 447-450. doi:10.1136/jmg.22.6.447
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Immunogenetic studies in families with rheumatoid arthritis and autoimmune thyroid disease.
P A Sanders, D M Grennan, P A Dyer, G G de Lange, and R Harris
J Med Genet 1985; 22: 451-456. doi:10.1136/jmg.22.6.451
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Should women at high risk of neural tube defect have an amniocentesis?
K M Laurence, G Elder, K T Evans, B M Hibbard, M Hoole, and C J Roberts
J Med Genet 1985; 22: 457-461. doi:10.1136/jmg.22.6.457
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Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probe.
M E Pembrey, J M Old, J V Leonard, C H Rodeck, R Warren, and K E Davies
J Med Genet 1985; 22: 462-465. doi:10.1136/jmg.22.6.462
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Collagen genes and proteins in osteogenesis imperfecta.
F M Pope, A C Nicholls, J McPheat, P Talmud, and R Owen
J Med Genet 1985; 22: 466-478. doi:10.1136/jmg.22.6.466
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The acetylator phenotypes of Saudi Arabian diabetics.
D A Evans, S Paterson, P Francisco, and G Alvarez
J Med Genet 1985; 22: 479-483. doi:10.1136/jmg.22.6.479
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Familial complex autosomal translocations involving chromosomes 7, 8, and 9 exhibiting male and female transmission with segregation and recombination.
S Walker, P J Howard, and D Hunter
J Med Genet 1985; 22: 484-491. doi:10.1136/jmg.22.6.484
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HLA antigens in psoriasis and psoriatic arthritis.
J C Woodrow and A Ilchysyn
J Med Genet 1985; 22: 492-495. doi:10.1136/jmg.22.6.492
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