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| September 1966 (Volume 3, Number 3). [Index by author] | ||
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Articles
Miscellaneous
Articles
Book Reviews
Research Article
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Table of Contents (PDF) | Cover (PDF)
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Turner's Syndrome in a Phenotypic Male with XO/XY Mosaicism and Autosomal Aberrations Alide M. C. Urmenyi, Myra K. Beattie, and M. R. Mirza J Med Genet 1966; 3: 220-225. doi:10.1136/jmg.3.3.220 |
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Corrigendum J Med Genet 1966; 3: 238. doi:10.1136/jmg.3.3.238 |
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Turner's Syndrome in a Phenotypic Male with XO/XY Mosaicism and Autosomal Aberrations Alide M. C. Urmenyi, Myra K. Beattie, and M. R. Mirza J Med Genet 1966; 3: 220-225. doi:10.1136/jmg.3.3.220 |
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Renal Tubular Dysfunction J Med Genet 1966; 3: 237. doi:10.1136/jmg.3.3.237 |
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Book Reviews J Med Genet 1966; 3: 237-238. doi:10.1136/jmg.3.3.237-a |
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Expectation of abnormality on paternal and maternal sides: a computational model. E Slater J Med Genet 1966; 3: 159-161. doi:10.1136/jmg.3.3.159 |
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The X-linked blood group system Xg tests on British, Northern American, and northern European unrelated people and families. J Noades, J Gavin, P Tippett, R Sanger, and R R Race J Med Genet 1966; 3: 162-168. doi:10.1136/jmg.3.3.162 |
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Gene effect in carriers of anhidrotic ectodermal dysplasia. C B Kerr, R S Wells, and K E Cooper J Med Genet 1966; 3: 169-176. doi:10.1136/jmg.3.3.169 |
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Haemoglobin genotypes, ABO blood groups, and Burkitt's tumour. A O Williams J Med Genet 1966; 3: 177-179. doi:10.1136/jmg.3.3.177 |
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Blood group changes in leukaemia. M Ayres, F M Salzano, and O K Ludwig J Med Genet 1966; 3: 180-185. doi:10.1136/jmg.3.3.180 |
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Satellite association and translocation mongolism. H Zellweger, G Abbo, and R Cuany J Med Genet 1966; 3: 186-189. doi:10.1136/jmg.3.3.186 |
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The silent gene for serum pseudocholinesterase. A Szeinberg, S Pipano, E Ostfeld, and L Eviatar J Med Genet 1966; 3: 190-193. doi:10.1136/jmg.3.3.190 |
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Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency. G Gaull and M K Gaitonde J Med Genet 1966; 3: 194-197. doi:10.1136/jmg.3.3.194 |
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Genetic diversity in serum albumin. M S Adams J Med Genet 1966; 3: 198-202. doi:10.1136/jmg.3.3.198 |
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The use of the surname as a genetic marker in Wales. D J Ashley and H D Davies J Med Genet 1966; 3: 203-211. doi:10.1136/jmg.3.3.203 |
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A monopodal sireniform monster with dermatoglyphic and cytogenetic studies. M D Crawfurd, S R Ismail, and J S Wigglesworth J Med Genet 1966; 3: 212-216. doi:10.1136/jmg.3.3.212 |
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A pair of twins, one of whom has chronic granulocytic leukaemia. L Dougan, I D Scott, and H J Woodliff J Med Genet 1966; 3: 217-219. doi:10.1136/jmg.3.3.217 |
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Apparent deletion of X chromosome in a prepuberal girl. E Steinberger, A Steinberger, K D Smith, and W H Perloff J Med Genet 1966; 3: 226-229. doi:10.1136/jmg.3.3.226 |
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A proposed classification of genetically determined mosaicism in man. M J Corey and J R Miller J Med Genet 1966; 3: 230-236. doi:10.1136/jmg.3.3.230 |
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