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| September 1971 (Volume 8, Number 3). [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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Genetic Concepts and Neoplasia A. G. Baikie J Med Genet 1971; 8: 395. doi:10.1136/jmg.8.3.395 |
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Elements of Medical Genetics Sarah Bundey J Med Genet 1971; 8: 395. doi:10.1136/jmg.8.3.395-a |
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Birth Defects; Original Article Series, V. 4 Ruth Wynne-Davies J Med Genet 1971; 8: 395-396. doi:10.1136/jmg.8.3.395-b |
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The Post-natal Development of Phenotype H. Kalmus J Med Genet 1971; 8: 396. doi:10.1136/jmg.8.3.396 |
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Genetic Epistemology J. H. Edwards J Med Genet 1971; 8: 396. doi:10.1136/jmg.8.3.396-a |
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Advances in Twin Studies M. G. Bulmer J Med Genet 1971; 8: 396-397. doi:10.1136/jmg.8.3.396-b |
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Klassische und Molekulare Genetik Arnold Sorsby J Med Genet 1971; 8: 397. doi:10.1136/jmg.8.3.397 |
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Genetic Counselling C. O. Carter J Med Genet 1971; 8: 397. doi:10.1136/jmg.8.3.397-a |
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Human Genetics and Medicine C. O. Carter J Med Genet 1971; 8: 397-398. doi:10.1136/jmg.8.3.397-b |
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Cold Spring Harbor Symposia on Quantitative Biology, Vol. XXXV Richard S. Hayward J Med Genet 1971; 8: 398. doi:10.1136/jmg.8.3.398 |
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Polycystic disease of kidney and liver presenting in childhood. H Blyth and B G Ockenden J Med Genet 1971; 8: 257-284. doi:10.1136/jmg.8.3.257 |
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Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance. K Fried, E Liban, M Lurie, S Friedman, and S H Reisner J Med Genet 1971; 8: 285-290. doi:10.1136/jmg.8.3.285 |
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X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data. R M Bannerman, G B Ingall, and J F Mohn J Med Genet 1971; 8: 291-301. doi:10.1136/jmg.8.3.291 |
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Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S. F I Konotey-Ahulu, J L Kinderlerer, H Lehmann, and B Ringelhann J Med Genet 1971; 8: 302-305. doi:10.1136/jmg.8.3.302 |
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Differentiation of two genetically specific types of depression by the response to antidepressant drugs. C M Pare and J W Mack J Med Genet 1971; 8: 306-309. doi:10.1136/jmg.8.3.306 |
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Mutation rate in Duchenne muscular dystrophy. H K Goswami and B D Chaurasia J Med Genet 1971; 8: 310-311. doi:10.1136/jmg.8.3.310 |
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Familial total anomalous pulmonary venous return. J E Paz and E E Castilla J Med Genet 1971; 8: 312-314. doi:10.1136/jmg.8.3.312 |
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Distribution of ABO blood groups, G6PD deficiency, and abnormal haemoglobins in leprosy. N Saha, H B Wong, B Banerjee, and M O Wong J Med Genet 1971; 8: 315-316. doi:10.1136/jmg.8.3.315 |
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Rh immunization following incompatible blood transfusion and a possible long-term complication of anti-D immunoglobulin therapy. M E Beard, J Pemberton, J Blagdon, and W F Jenkins J Med Genet 1971; 8: 317-320. doi:10.1136/jmg.8.3.317 |
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Suppression of the immune response. J Bradley and C J Elson J Med Genet 1971; 8: 321-340. doi:10.1136/jmg.8.3.321 |
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Group G deletion syndromes. R P Kelch, M Franklin, and R D Schmickel J Med Genet 1971; 8: 341-345. doi:10.1136/jmg.8.3.341 |
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The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+). J Chemke and A Robinson J Med Genet 1971; 8: 346-350. doi:10.1136/jmg.8.3.346 |
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The 13q- deletion syndrome. E Grace, J Drennan, D Colver, and R R Gordon J Med Genet 1971; 8: 351-357. doi:10.1136/jmg.8.3.351 |
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Somatic stigmata of Turner's syndrome in a patient with 46,XXq-. M Bocian, E Krmpotic, K Szego, and I M Rosenthal J Med Genet 1971; 8: 358-363. doi:10.1136/jmg.8.3.358 |
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Klinefelter's syndrome and G trisomy. B Erdtmann, A A de Freitas, R P de Souza, and F M Salzano J Med Genet 1971; 8: 364-368. doi:10.1136/jmg.8.3.364 |
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A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation. H Grotsky, L Y Hsu, and K Hirschhorn J Med Genet 1971; 8: 369-371. doi:10.1136/jmg.8.3.369 |
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A prisoner with an unusual karyotype (46,XY,Dq-). J Kahn and F Reed J Med Genet 1971; 8: 372-373. doi:10.1136/jmg.8.3.372 |
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Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient. P Genest, M Bouchard, and J Poty J Med Genet 1971; 8: 374-377. doi:10.1136/jmg.8.3.374 |
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An extra small metacentric autosome in a mentally retarded boy with multiple malformations. S Armendares, L Buentello, and F Salamanca J Med Genet 1971; 8: 378-380. doi:10.1136/jmg.8.3.378 |
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An extra small metacentric chromosome in association with multiple congenital abnormalities. W H Finley, S C Finley, and D Monsky J Med Genet 1971; 8: 381-383. doi:10.1136/jmg.8.3.381 |
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Trisomy D-trisomy E mosaicism in an infant male. R J Warren and J I Keith J Med Genet 1971; 8: 384-386. doi:10.1136/jmg.8.3.384 |
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X chromosome long arm deletion in a patient with Down's syndrome. F W Luthardt and C G Palmer J Med Genet 1971; 8: 387-391. doi:10.1136/jmg.8.3.387 |
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Trisomy 18 in one of fraternal twins. D Gertzer and G Nathenson J Med Genet 1971; 8: 392-394. doi:10.1136/jmg.8.3.392 |
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