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| December 1966 (Volume 3, Number 4). [Index by author] | ||
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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The Increased Risk of Death from Ischaemic Heart Disease in First Degree Relatives of 121 Men and 96 Women with Ischaemic Heart Disease J. Slack and K. A. Evans J Med Genet 1966; 3: 239-257. doi:10.1136/jmg.3.4.239 |
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A Complex Pattern of Chromosome Abnormalities in the Acute Phase of Chronic Granulocytic Leukaemia P. H. Fitzgerald J Med Genet 1966; 3: 258-264. doi:10.1136/jmg.3.4.258 |
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Familial Camptodactyly with Taurinuria N. C. Nevin, L. J. Hurwitz, and D. W. Neill J Med Genet 1966; 3: 265-268. doi:10.1136/jmg.3.4.265 |
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Family Studies on Ocular Refraction and Its Components Arnold Sorsby, G. A. Leary, and G. R. Fraser J Med Genet 1966; 3: 269-273. doi:10.1136/jmg.3.4.269 |
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Astrocytomas and the ABO Blood Groups R. R. Strang, D. Tovi, and J. Lopez J Med Genet 1966; 3: 274-275. doi:10.1136/jmg.3.4.274 |
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Distribution of Haptoglobin Subtypes in Greeks B. Angelopoulos, A. Tsoukantas, and E. Danopoulos J Med Genet 1966; 3: 276-278. doi:10.1136/jmg.3.4.276 |
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Haptoglobin Phenotypes Among Egyptians Nemat Hashem, K. Kamel, and E. I. Hammoud J Med Genet 1966; 3: 279-280. doi:10.1136/jmg.3.4.279 |
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Quantitative Variations of Haptoglobins in a Caucasian Family G. I. Higashi and H. A. Lubs, Jr. J Med Genet 1966; 3: 281-284. doi:10.1136/jmg.3.4.281 |
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The Increased Risk of Death from Ischaemic Heart Disease in First Degree Relatives of 121 Men and 96 Women with Ischaemic Heart Disease J. Slack and K. A. Evans J Med Genet 1966; 3: 239-257. doi:10.1136/jmg.3.4.239 |
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A Complex Pattern of Chromosome Abnormalities in the Acute Phase of Chronic Granulocytic Leukaemia P. H. Fitzgerald J Med Genet 1966; 3: 258-264. doi:10.1136/jmg.3.4.258 |
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Familial Camptodactyly with Taurinuria N. C. Nevin, L. J. Hurwitz, and D. W. Neill J Med Genet 1966; 3: 265-268. doi:10.1136/jmg.3.4.265 |
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Family Studies on Ocular Refraction and Its Components Arnold Sorsby, G. A. Leary, and G. R. Fraser J Med Genet 1966; 3: 269-273. doi:10.1136/jmg.3.4.269 |
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Astrocytomas and the ABO Blood Groups R. R. Strang, D. Tovi, and J. Lopez J Med Genet 1966; 3: 274-275. doi:10.1136/jmg.3.4.274 |
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Distribution of Haptoglobin Subtypes in Greeks B. Angelopoulos, A. Tsoukantas, and E. Danopoulos J Med Genet 1966; 3: 276-278. doi:10.1136/jmg.3.4.276 |
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Haptoglobin Phenotypes Among Egyptians Nemat Hashem, K. Kamel, and E. I. Hammoud J Med Genet 1966; 3: 279-280. doi:10.1136/jmg.3.4.279 |
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Quantitative Variations of Haptoglobins in a Caucasian Family G. I. Higashi and H. A. Lubs, Jr. J Med Genet 1966; 3: 281-284. doi:10.1136/jmg.3.4.281 |
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The Metabolic Basis of Inherited Disease, 2nd ed J Med Genet 1966; 3: 315. doi:10.1136/jmg.3.4.315 |
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Book Reviews J Med Genet 1966; 3: 315-316. doi:10.1136/jmg.3.4.315-a |
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New Directions in Human Genetics. A Symposium J Med Genet 1966; 3: 316. doi:10.1136/jmg.3.4.316 |
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Die Angeborenen Fehlbildungen der Hand und ihre Operative Behandlung J Med Genet 1966; 3: 316. doi:10.1136/jmg.3.4.316-a |
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Malformations Associées de la Tête et des Extrémités J Med Genet 1966; 3: 316. doi:10.1136/jmg.3.4.316-b |
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Symphalangism: A Pedigree from South India Gemma Savarinathan and Willard R. Centerwall J Med Genet 1966; 3: 285-289. doi:10.1136/jmg.3.4.285 |
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Apparent Monosomy of a G Autosome in a Jamaican Infant Marigold J. Thorburn and Barbara E. Johnson J Med Genet 1966; 3: 290-292. doi:10.1136/jmg.3.4.290 |
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A Fatal Congenital Defect Associated with a Unique Chromosome Abnormality A. D. Bain and I. K. Gauld J Med Genet 1966; 3: 293-294. doi:10.1136/jmg.3.4.293 |
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An Extra Small Metacentric Chromosome in a Female Child Robert F. Tamburro and Charles E. Johnson J Med Genet 1966; 3: 295-297. doi:10.1136/jmg.3.4.295 |
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Huntington's Chorea Ntinos C. Myrianthopoulos J Med Genet 1966; 3: 298-314. doi:10.1136/jmg.3.4.298 |
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