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| December 1968 (Volume 5, Number 4). [Index by author] | ||
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Book Review
Research Article
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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Books and Monographs: The Origin of Life Arnold Sorsby J Med Genet 1968; 5: 360. doi:10.1136/jmg.5.4.360 |
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Books and Monographs: Clinical Genetics in Psychiatry. Problems in Nosological Classification Eliot Slater J Med Genet 1968; 5: 360-361. doi:10.1136/jmg.5.4.360-a |
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Books and Monographs: A Neuropsychiatric and Genetical Investigation of Acute Intermittent Porphyria Eliot Slater J Med Genet 1968; 5: 361-362. doi:10.1136/jmg.5.4.361 |
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Books and Monographs: Biological Psychiatry John Price J Med Genet 1968; 5: 362. doi:10.1136/jmg.5.4.362 |
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Books and Monographs: Sex Chromosomes and Sex Linked Genes John L. Hamerton J Med Genet 1968; 5: 363. doi:10.1136/jmg.5.4.363 |
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Books and Monographs: Humangenetik. Ein kurzes Handbuch in fünf Bänden. Band I/1 Grundlinien, Terminologie, Methoden, Geschichte der Humangenetik, Abstammungsgeschichte, Chromosomen, Mass und Formmerkmale, Entwicklung, Konstitution, Geschlecht, Normale Merkmale von Haut-und Anhanggebilden Arnold Sorsby J Med Genet 1968; 5: 363-364. doi:10.1136/jmg.5.4.363-a |
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Books and Monographs: Recent Results in Cancer Research C. A. Clarke J Med Genet 1968; 5: 364. doi:10.1136/jmg.5.4.364 |
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Surveys, Symposia, and Transactions: Progress in Medical Genetics R. Harris J Med Genet 1968; 5: 364-365. doi:10.1136/jmg.5.4.364-a |
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Surveys, Symposia, and Transactions: Annual Review of Genetics, Volume 1, 1967 Martin Bobrow J Med Genet 1968; 5: 365. doi:10.1136/jmg.5.4.365 |
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Surveys, Symposia, and Transactions: Proceedings of the Third International Congress of Human Genetics A. C. Stevenson J Med Genet 1968; 5: 365. doi:10.1136/jmg.5.4.365-a |
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Surveys, Symposia, and Transactions: Symposium on Autoimmunity and Genetics J. H. Thomson J Med Genet 1968; 5: 365-366. doi:10.1136/jmg.5.4.365-b |
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Surveys, Symposia, and Transactions: Phenotypic Expression. Immunological, Biochemical, and Morphological Joseph Chayen J Med Genet 1968; 5: 366. doi:10.1136/jmg.5.4.366 |
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Surveys, Symposia, and Transactions: Primates in Medicine J. H. Thomson J Med Genet 1968; 5: 366. doi:10.1136/jmg.5.4.366-a |
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Surveys, Symposia, and Transactions: Cell Differentiation J. Chayen J Med Genet 1968; 5: 366-367. doi:10.1136/jmg.5.4.366-b |
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Surveys, Symposia, and Transactions: Social and Genetic Influences on Life and Death Arnold Sorsby J Med Genet 1968; 5: 367. doi:10.1136/jmg.5.4.367 |
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Surveys, Symposia, and Transactions: Pathogenesis of Nervous and Mental Diseases in Children Valerie Cowie J Med Genet 1968; 5: 367. doi:10.1136/jmg.5.4.367-a |
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Surveys, Symposia, and Transactions: Comptes Rendus du 1er Congrès International de Neurogénétique et Neuro-optalmologie Arnold Sorsby J Med Genet 1968; 5: 367. doi:10.1136/jmg.5.4.367-b |
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Surveys, Symposia, and Transactions: Probleme der molekularen und allgemeinen Biologie der Zelle. 3.Gesamttagung der Deutschen Gesellschaft für experimentelle Medizin Joseph Chayen J Med Genet 1968; 5: 368. doi:10.1136/jmg.5.4.368 |
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New Editions: The Causes of Evolution J Med Genet 1968; 5: 368. doi:10.1136/jmg.5.4.368-a |
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New Editions: Genetics for Medical Students J Med Genet 1968; 5: 368. doi:10.1136/jmg.5.4.368-b |
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Genetic study of sample of 70 patients with myasthenia gravis. A Jacob, E R Clack, and A E Emery J Med Genet 1968; 5: 257-261. doi:10.1136/jmg.5.4.257 |
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Incidence of fibrocystic disease in Wessex. B D Hall and M J Simpkiss J Med Genet 1968; 5: 262-265. doi:10.1136/jmg.5.4.262 |
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Multiple sclerosis: discordance in three pairs of dizygotic twins. W S Cendrowski J Med Genet 1968; 5: 266-268. doi:10.1136/jmg.5.4.266 |
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Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies. R S Rapp and W E Hodgkin J Med Genet 1968; 5: 269-272. doi:10.1136/jmg.5.4.269 |
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Diagnostic and genetical aspects of tuberous sclerosis. N C Nevin and W G Pearce J Med Genet 1968; 5: 273-280. doi:10.1136/jmg.5.4.273 |
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Amino acid patterns in cystinuric families. S Kelly and W Copeland J Med Genet 1968; 5: 281-285. doi:10.1136/jmg.5.4.281 |
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Testosterone excretion rates in normal males and males with an XYY complement. B T Rudd, O M Galal, and M D Casey J Med Genet 1968; 5: 286-288. doi:10.1136/jmg.5.4.286 |
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Familial microtia with meatal atresia in two sibships. L C Ellwood, S T Winter, and H Dar J Med Genet 1968; 5: 289-291. doi:10.1136/jmg.5.4.289 |
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Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline. R W Opfell, P A Lorkin, and H Lehmann J Med Genet 1968; 5: 292-297. doi:10.1136/jmg.5.4.292 |
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Combination of hereditary elliptocytosis and heterozygous beta-thalassaemia: a family study. M Aksoy and S Erdem J Med Genet 1968; 5: 298-301. doi:10.1136/jmg.5.4.298 |
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Secretor status in asthma and hay fever. M A Denborough and H J Downing J Med Genet 1968; 5: 302-305. doi:10.1136/jmg.5.4.302 |
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Incidence of ABO and RH blood groups in pulmonary tuberculosis in different ethnic groups. N Saha and B Banerjee J Med Genet 1968; 5: 306-307. doi:10.1136/jmg.5.4.306 |
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ABO blood groups and vitiligo. V N Sehgal and B Dube J Med Genet 1968; 5: 308-309. doi:10.1136/jmg.5.4.308 |
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Further observations on Kell blood groups in families ascertained via a mongol propositus. D A Evans, P J Wren, W T Donohoe, M F Bullen, M Lewis, H Kaita, B Chown, and I Uchida J Med Genet 1968; 5: 310-313. doi:10.1136/jmg.5.4.310 |
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Diverse chromosomal anomalies in a family. L Atkins, C S Bartsocas, and P J Porter J Med Genet 1968; 5: 314-318. doi:10.1136/jmg.5.4.314 |
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Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs. W H Galloway and A P Mowat J Med Genet 1968; 5: 319-321. doi:10.1136/jmg.5.4.319 |
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A large deletion of chromosome no. 1 (46,XY,1?--). D Aarskog J Med Genet 1968; 5: 322-325. doi:10.1136/jmg.5.4.322 |
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X-linked hydrocephalus. M W Shannon and H L Nadler J Med Genet 1968; 5: 326-328. doi:10.1136/jmg.5.4.326 |
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Multiple anomalies associated with a small extra metacentric autosome. A B Mukherjee, M W Partington, N E Simpson, and K A Walmsley J Med Genet 1968; 5: 329-334. doi:10.1136/jmg.5.4.329 |
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An extra small metacentric chromosome in a mentally retarded boy. J Ishmael and K M Laurence J Med Genet 1968; 5: 335-340. doi:10.1136/jmg.5.4.335 |
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Males with an XYY sex chromosome complement. W M Brown J Med Genet 1968; 5: 341-359. doi:10.1136/jmg.5.4.341 |
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