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| June 1970 (Volume 7, Number 2). [Index by author] | ||
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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Grundriss der Genetik H. Kalmus J Med Genet 1970; 7: 189. doi:10.1136/jmg.7.2.189 |
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Nucleic Acid Metabolism Cell Differentiation and Cancer Growth: Proceedings of the second international symposium for cellular chemistry J. Chayen J Med Genet 1970; 7: 189-190. doi:10.1136/jmg.7.2.189-a |
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Progress in Medical Genetics A. E. H. Emery J Med Genet 1970; 7: 190. doi:10.1136/jmg.7.2.190 |
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The Chromosome Disorders. An Introduction for Clinicians John L. Hamerton J Med Genet 1970; 7: 190-191. doi:10.1136/jmg.7.2.190-a |
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Human Afflictions and Chromosome Abberations John L. Hamerton J Med Genet 1970; 7: 191. doi:10.1136/jmg.7.2.191 |
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Chromosomes and Genes. The Biological Basis of Heredity John L. Hamerton J Med Genet 1970; 7: 191. doi:10.1136/jmg.7.2.191-a |
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The Elements of Cytogenetics John L. Hamerton J Med Genet 1970; 7: 191. doi:10.1136/jmg.7.2.191-b |
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Endocrinopatile Genetice Arnold Sorsby J Med Genet 1970; 7: 191-192. doi:10.1136/jmg.7.2.191-c |
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Gene Activity in Early Development Ursula Mittwoch J Med Genet 1970; 7: 192. doi:10.1136/jmg.7.2.192 |
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Familial XY gonadal dysgenesis. J Chemke, R Carmichael, J M Stewart, R H Geer, and A Robinson J Med Genet 1970; 7: 105-111. doi:10.1136/jmg.7.2.105 |
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Relation of face shape to susceptibility to congenital cleft lip. A preliminary report. F C Fraser and H Pashayan J Med Genet 1970; 7: 112-117. doi:10.1136/jmg.7.2.112 |
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Chromosome abnormalities in early spontaneous abortions. D T Arakaki and S H Waxman J Med Genet 1970; 7: 118-124. doi:10.1136/jmg.7.2.118 |
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Dermatoglyphs in leukaemia. J L Verbov J Med Genet 1970; 7: 125-131. doi:10.1136/jmg.7.2.125 |
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Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence. F C Yu, L T Gutman, S W Huang, J W Fresh, and I Emanuel J Med Genet 1970; 7: 132-137. doi:10.1136/jmg.7.2.132 |
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Trisomy 18 syndrome in Chinese infants. Clinical findings and incidence. I Emanuel, S W Huang, W T Chiang, and C P Yang J Med Genet 1970; 7: 138-141. doi:10.1136/jmg.7.2.138 |
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Significance of chromosome 17ps+ in three generations of a family. J H Priest, D C Peakman, S R Patil, and A Robinson J Med Genet 1970; 7: 142-147. doi:10.1136/jmg.7.2.142 |
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Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women. M A Ridler, J M Berg, M J Pendrey, P Saldaña, and J A Timothy J Med Genet 1970; 7: 148-152. doi:10.1136/jmg.7.2.148 |
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Recessive albinism in three children and both parents. M Oliver and K Fried J Med Genet 1970; 7: 153-154. doi:10.1136/jmg.7.2.153 |
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Von Hippel-Lindau syndrome: a report on three kindreds. M H Shokeir J Med Genet 1970; 7: 155-157. doi:10.1136/jmg.7.2.155 |
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Familial hypertrichosis cubiti: hairy elbows syndrome. P Beighton J Med Genet 1970; 7: 158-160. doi:10.1136/jmg.7.2.158 |
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A 45,XY,5-15-,t(5q15q) cri-du-chat child. L Jackson and M Barr J Med Genet 1970; 7: 161-163. doi:10.1136/jmg.7.2.161 |
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Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4. M G Wilson, J W Towner, and L D Negus J Med Genet 1970; 7: 164-170. doi:10.1136/jmg.7.2.164 |
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Deletion of short arm of no. 4 (4p-)--a detailed case report. A R Wilcock, F G Adams, P Cooke, and R R Gordon J Med Genet 1970; 7: 171-176. doi:10.1136/jmg.7.2.171 |
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Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr). G Gacs, D Schuler, and M Sellyei J Med Genet 1970; 7: 177-179. doi:10.1136/jmg.7.2.177 |
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Developmental abnormalities in a patient with karyotype 46,XX,bq+. J E Chakanovskis and G R Sutherland J Med Genet 1970; 7: 180-184. doi:10.1136/jmg.7.2.180 |
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Hemifacial microsomia--oculo-auriculo-vertebral dysplasia. A patient with overlapping features. H Pashayan, L Pinsky, and F C Fraser J Med Genet 1970; 7: 185-188. doi:10.1136/jmg.7.2.185 |
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