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| June 1971 (Volume 8, Number 2). [Index by author] | ||
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Miscellaneous
Correspondence
Book Review
Research Article
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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Corrigendum J Med Genet 1971; 8: 254. doi:10.1136/jmg.8.2.254 |
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Correspondence Marigold J. Thorburn J Med Genet 1971; 8: 250. doi:10.1136/jmg.8.2.250 |
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Birth Defects: Original Article Series, V, 3 Ruth Wynne-Davies J Med Genet 1971; 8: 251. doi:10.1136/jmg.8.2.251 |
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Birth Defects: Original Article Series, V, 2 J. Insley J Med Genet 1971; 8: 251-252. doi:10.1136/jmg.8.2.251-a |
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Alzheimer's Disease and Related Conditions E. Slater J Med Genet 1971; 8: 252. doi:10.1136/jmg.8.2.252 |
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Serendipity in St. Helena. A Genetical and Medical Study of an Isolated Community Arnold Sorsby J Med Genet 1971; 8: 252. doi:10.1136/jmg.8.2.252-a |
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The De Lange Syndrome Sarah Bundey J Med Genet 1971; 8: 252-253. doi:10.1136/jmg.8.2.252-b |
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Epidemiology of Mongolism C. O. Carter J Med Genet 1971; 8: 253. doi:10.1136/jmg.8.2.253 |
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An ABC of Medical Genetics M. A. Ferguson-Smith J Med Genet 1971; 8: 253-254. doi:10.1136/jmg.8.2.253-a |
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Genetic control of nortriptyline kinetics in man: a study of relatives of propositi with high plasma concentrations. M Asberg, D A Evans, and F Sjöqvist J Med Genet 1971; 8: 129-135. doi:10.1136/jmg.8.2.129 |
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The genetic basis of variation in factor 8 levels among haemophiliacs. D F Roberts J Med Genet 1971; 8: 136-139. doi:10.1136/jmg.8.2.136 |
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Ahaptoglobinaemia and predisposition to iron-deficiency anaemia. E S Azevêdo, S Assemany, M M Martins de Souza, and M E Almeida Santana J Med Genet 1971; 8: 140-142. doi:10.1136/jmg.8.2.140 |
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Genetics of childhood spinal muscular atrophy. E J Winsor, E G Murphy, M W Thompson, and T E Reed J Med Genet 1971; 8: 143-148. doi:10.1136/jmg.8.2.143 |
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Double heterozygosity for glucose-6-phosphate dehydrogenase deficiency. T K Chan and M C Lai J Med Genet 1971; 8: 149-152. doi:10.1136/jmg.8.2.149 |
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Genetic studies on hypospadias in males. Y C Chen and P V Woolley, Jr J Med Genet 1971; 8: 153-159. doi:10.1136/jmg.8.2.153 |
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Virilizing adrenal carcinoma in two sibs. M Mahloudji, H Ronaghy, and W Dutz J Med Genet 1971; 8: 160-163. doi:10.1136/jmg.8.2.160 |
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Chromosome studies in selected spontaneous abortions. Polyploidy in man. D H Carr J Med Genet 1971; 8: 164-174. doi:10.1136/jmg.8.2.164 |
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Fertility in balanced heterozygotes for a familial centric fusion translocation, t(DgDg). J A Wilson J Med Genet 1971; 8: 175-178. doi:10.1136/jmg.8.2.175 |
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47,XX,13+ with Snodgrass phenotype II. Are different chromosomes associated with two clinical varieties of D-trisomy? R L Neu, S R Assemany, and L I Gardner J Med Genet 1971; 8: 179-180. doi:10.1136/jmg.8.2.179 |
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Chromosomal aberrations induced by T strains mycoplasmas. R B Kundsin, M Ampola, S Streeter, and P Neurath J Med Genet 1971; 8: 181-187. doi:10.1136/jmg.8.2.181 |
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A family with balanced translocation, t(5p-;Gp+). B J White, L C Van de Water, and J Tjio J Med Genet 1971; 8: 188-194. doi:10.1136/jmg.8.2.188 |
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Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases. V Dubowitz, P Cooke, D Colver, and F Harris J Med Genet 1971; 8: 195-201. doi:10.1136/jmg.8.2.195 |
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A familial variant of chromosome 9. C G Palmer and J Schroder J Med Genet 1971; 8: 202-208. doi:10.1136/jmg.8.2.202 |
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Di Guglielmo syndrome in a t(DgDg) heterozygote. B Dallapiccola and P Malacarne J Med Genet 1971; 8: 209-214. doi:10.1136/jmg.8.2.209 |
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A case of XYY Down's syndrome confirmed by autoradiography. R Laxova, J A McKeown, P Saldaña, and J A Timothy J Med Genet 1971; 8: 215-219. doi:10.1136/jmg.8.2.215 |
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49,XXXXY chromossomal anomaly in a neonate. A Hayek, V Riccardi, L Atkins, and H Hendren J Med Genet 1971; 8: 220-221. doi:10.1136/jmg.8.2.220 |
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Ring 13 chromosome with normal haptoglobin inheritance. J G Hollowell, L G Littlefield, A Dharmkrong-AT, G M Folger, C W Heath, Jr, and G E Bloom J Med Genet 1971; 8: 222-226. doi:10.1136/jmg.8.2.222 |
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A group-C ring chromosome in a mentally deficient male. A J Therkelsen, B Moller, and K Henningsen J Med Genet 1971; 8: 227-230. doi:10.1136/jmg.8.2.227 |
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A child with a ring G chromosome (46,XX, Gr). N C Nevin, B MacLaverty, and W A Campbell J Med Genet 1971; 8: 231-234. doi:10.1136/jmg.8.2.231 |
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A complex chromosomal rearrangement with formation of a ring 4. M Bobrow, L F Joness, and G Clarke J Med Genet 1971; 8: 235-239. doi:10.1136/jmg.8.2.235 |
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The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities. M Bobrow and P L Pearson J Med Genet 1971; 8: 240-243. doi:10.1136/jmg.8.2.240 |
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Additional G-like chromosome in a malformed boy. M Fraccaro, M Hultén, S D Jayakar, A Lindsjö, J Lindsten, and L Tiepolo J Med Genet 1971; 8: 244-249. doi:10.1136/jmg.8.2.244 |
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