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| June 1969 (Volume 6, Number 2). [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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Books and Monographs: Blood Groups in Man H. Lehmann J Med Genet 1969; 6: 228. doi:10.1136/jmg.6.2.228 |
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Books and Monographs: The Congenital Methemoglobinemias. Physiology and Pathophysiology of the Methemoglobin Metabolism J. V. Dacie J Med Genet 1969; 6: 228-229. doi:10.1136/jmg.6.2.228-a |
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Books and Monographs: An Atlas of Mammalian Chromosomes John L. Hamerton J Med Genet 1969; 6: 229. doi:10.1136/jmg.6.2.229 |
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Books and Monographs: Primer of Chromosome Practice. Plant and Animal Chromosomes Under the Microscope John L. Hamerton J Med Genet 1969; 6: 229. doi:10.1136/jmg.6.2.229-a |
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Books and Monographs: Elements of Medical Genetics C. O. Carter J Med Genet 1969; 6: 229. doi:10.1136/jmg.6.2.229-b |
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Books and Monographs: Evolutionsprozesse. Einzelvorgänge im Wandel der Organismen. Grundbegriffe der modernen Biologie H. Lehmann J Med Genet 1969; 6: 230. doi:10.1136/jmg.6.2.230 |
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Books and Monographs: A Dictionary of Genetics Arnold Sorsby J Med Genet 1969; 6: 230. doi:10.1136/jmg.6.2.230-a |
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Books and Monographs: Biophysical Technique as Applied to Cell Biology N. B. Atkin J Med Genet 1969; 6: 230. doi:10.1136/jmg.6.2.230-b |
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Surveys, Symposia, and Transactions: Research in Muscular Dystrophy C. A. Clarke J Med Genet 1969; 6: 231. doi:10.1136/jmg.6.2.231 |
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Surveys, Symposia, and Transactions: Screening in Medical Care. Reviewing the Evidence J. H. Edwards J Med Genet 1969; 6: 231-232. doi:10.1136/jmg.6.2.231-a |
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Shorter Notices: Forerunners of Darwin, 1745-1859 J Med Genet 1969; 6: 232. doi:10.1136/jmg.6.2.232 |
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Shorter Notices: Genetische Familienberatung. Ein Leitfaden für den Artz J Med Genet 1969; 6: 232. doi:10.1136/jmg.6.2.232-a |
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Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance. L Dallaire J Med Genet 1969; 6: 113-120. doi:10.1136/jmg.6.2.113 |
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An association of Rh type and gynaecological disease with twinning. F V De George J Med Genet 1969; 6: 121-125. doi:10.1136/jmg.6.2.121 |
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Hypertrophic pyloric stenosis: adult and congenital types occurring in the same family. C Zavala, A Bolio, R Montalvo, and R Lisker J Med Genet 1969; 6: 126-128. doi:10.1136/jmg.6.2.126 |
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Inheritance of coeliac disease. W M McCrae J Med Genet 1969; 6: 129-131. doi:10.1136/jmg.6.2.129 |
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Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. K Fried, M Feinmesser, and J Tsitsianov J Med Genet 1969; 6: 132-134. doi:10.1136/jmg.6.2.132 |
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Mongolism and maternal menarche. J M Berg and J T Bavin J Med Genet 1969; 6: 135-136. doi:10.1136/jmg.6.2.135 |
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Consistent and variable chromosome anomalies in parents of children with Down's syndrome. J Kahn and K Abe J Med Genet 1969; 6: 137-149. doi:10.1136/jmg.6.2.137 |
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Studies on glucose-6-phosphate dehydrogenase deficient Egyptian families. N Hashem and A Nour J Med Genet 1969; 6: 150-156. doi:10.1136/jmg.6.2.150 |
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Comparison of strength of isoagglutinin titres in English and Finnish populations. I J Seppälä J Med Genet 1969; 6: 157-158. doi:10.1136/jmg.6.2.157 |
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XYY syndrome, and XYY-XXYY mosaicism also showing features of Klinefelter's syndrome. D A Spencer, J W Eyles, and M K Mason J Med Genet 1969; 6: 159-165. doi:10.1136/jmg.6.2.159 |
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Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p). C G Palmer, P M Conneally, and J C Christian J Med Genet 1969; 6: 166-173. doi:10.1136/jmg.6.2.166 |
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Familial transmission of a chromosomal translocation t(2q+;Cp-). C B Lozzio and A A Kattine J Med Genet 1969; 6: 174-179. doi:10.1136/jmg.6.2.174 |
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Welshness and fertility. D J Ashley J Med Genet 1969; 6: 180-182. doi:10.1136/jmg.6.2.180 |
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Blood groups and lung cancer. D J Ashley J Med Genet 1969; 6: 183-186. doi:10.1136/jmg.6.2.183 |
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A haptoglobin Johnson family with nonhypohaptoglobinaemic HpJ-Hp2. J Pintera, R Dvorák, J Vacl, and J Fiser J Med Genet 1969; 6: 187-189. doi:10.1136/jmg.6.2.187 |
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Further evidence for close linkage of the Hb-beta and Hb-delta loci in man. M K Mishu and W E Nance J Med Genet 1969; 6: 190-192. doi:10.1136/jmg.6.2.190 |
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Familial jaw cysts in Charcot-Marie-Tooth disease. M R Swift and S L Horowitz J Med Genet 1969; 6: 193-195. doi:10.1136/jmg.6.2.193 |
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Postaxial polydactyly in three Indian families. J Mohan J Med Genet 1969; 6: 196-200. doi:10.1136/jmg.6.2.196 |
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Partial trisomy in a child with features suggesting mongolism. H K Kumbnani and R A Pfeiffer J Med Genet 1969; 6: 201-205. doi:10.1136/jmg.6.2.201 |
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46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome. L Atkins and M Feingold J Med Genet 1969; 6: 206-208. doi:10.1136/jmg.6.2.206 |
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Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups. O M Garson, A G Baikie, J Ferguson, and C H Greer J Med Genet 1969; 6: 209-215. doi:10.1136/jmg.6.2.209 |
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A patient with a short arm deletion of chromosome 18 (46,XY,18p-). L Weiss and K Mayeda J Med Genet 1969; 6: 216-219. doi:10.1136/jmg.6.2.216 |
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A patient with 45,XX,Gminus-46,XX,Gr mosaicism. C E Blank and J Lorber J Med Genet 1969; 6: 220-223. doi:10.1136/jmg.6.2.220 |
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Congenital malformations associated with a ring 4 chromosome. R Carter, E Baker, and D Hayman J Med Genet 1969; 6: 224-227. doi:10.1136/jmg.6.2.224 |
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