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| September 1968 (Volume 5, Number 3). [Index by author] | ||
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Book Review
Research Article
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Table of Contents (PDF) | Cover (PDF)
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The Clinical Pathology of Infancy C. O. Carter J Med Genet 1968; 5: 253. doi:10.1136/jmg.5.3.253 |
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The Placenta in Twin Pregnancy N. Morris J Med Genet 1968; 5: 253. doi:10.1136/jmg.5.3.253-a |
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Karyotyp and Phänotyp der autosomalen Chromosomenarberrationen beim Menschen Ursula Mittwoch J Med Genet 1968; 5: 253-254. doi:10.1136/jmg.5.3.253-b |
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A Comparative Osteological Study of the Ainu and the Australian Aborigines J. G. Parish J Med Genet 1968; 5: 254. doi:10.1136/jmg.5.3.254 |
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An Epidemiological Survey of Skin Diseases, Tattooing, and Rheumatic Diseases as Exemplified Initially by the Prevalence of Psoriasis and Tattooing O. L. S. Scott J Med Genet 1968; 5: 255. doi:10.1136/jmg.5.3.255 |
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Translocation in Human Chromosomes with Special Reference to Mental Retardation and Congenital Malformations John Hamerton J Med Genet 1968; 5: 255-256. doi:10.1136/jmg.5.3.255-a |
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Biochemical Genetics H. Lehmann J Med Genet 1968; 5: 256. doi:10.1136/jmg.5.3.256 |
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Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents. A Froland, R Sanger, and R R Race J Med Genet 1968; 5: 161-164. doi:10.1136/jmg.5.3.161 |
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A survey of sex chromatin abnormalities in mental hospitals. N Maclean, W M Brown, P A Jacobs, D J Mantle, and J A Strong J Med Genet 1968; 5: 165-172. doi:10.1136/jmg.5.3.165 |
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Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients. H C Soltan J Med Genet 1968; 5: 173-180. doi:10.1136/jmg.5.3.173 |
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Genetical studies in testicular feminization syndrome. K Boczkowski J Med Genet 1968; 5: 181-188. doi:10.1136/jmg.5.3.181 |
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Inheritance in epidermolysis bullosa letalis. H E Cross, R S Wells, and J R Esterly J Med Genet 1968; 5: 189-196. doi:10.1136/jmg.5.3.189 |
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Abnormality on paternal and maternal sides: observations in schizophrenia and manic-depression. E Slater and M T Tsuang J Med Genet 1968; 5: 197-199. doi:10.1136/jmg.5.3.197 |
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New translocation in three generations of a family. P Cooke J Med Genet 1968; 5: 200-204. doi:10.1136/jmg.5.3.200 |
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A family with D-D translocation. E Krmpotic, K Ramanathan, and A Grossman J Med Genet 1968; 5: 205-210. doi:10.1136/jmg.5.3.205 |
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Down's syndrome with an unusual karyotype. M E Walker J Med Genet 1968; 5: 211-214. doi:10.1136/jmg.5.3.211 |
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XYY sex chromosomes in a Jamaican with orthopaedic abnormalities. M J Thorburn, W Chutkan, R Richards, and R Bell J Med Genet 1968; 5: 215-219. doi:10.1136/jmg.5.3.215 |
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A structurally abnormal chromosome (46,XX,?17p+) associated with mental deficiency and congenital malformations. N Ricci, B Dallapiccola, and B Ventimiglia J Med Genet 1968; 5: 220-223. doi:10.1136/jmg.5.3.220 |
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Karyotypes of cultured cells from foetal membranes of normal newborns. J A Böök, B Kjessler, and B Santesson J Med Genet 1968; 5: 224-226. doi:10.1136/jmg.5.3.224 |
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Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. A I Taylor J Med Genet 1968; 5: 227-252. doi:10.1136/jmg.5.3.227 |
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