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| March 1966 (Volume 3, Number 1). [Index by author] | ||
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Book Reviews
Research Article
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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Book Reviews J Med Genet 1966; 3: 76. doi:10.1136/jmg.3.1.76 |
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Diagnosis and Genetics of Defective Colour Vision J Med Genet 1966; 3: 76. doi:10.1136/jmg.3.1.76-a |
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Pyridoxine-responsive anaemia determined by an X-linked gene. M W Elves, M S Bourne, and M C Israëls J Med Genet 1966; 3: 1-4. doi:10.1136/jmg.3.1.1 |
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Juvenile polyposis coli. A M Veale, I McColl, H J Bussey, and B C Morson J Med Genet 1966; 3: 5-16. doi:10.1136/jmg.3.1.5 |
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Sex-linked cleft palate. Report of a family and review of 77 kindreds. E D Weinstein and M M Cohen J Med Genet 1966; 3: 17-22. doi:10.1136/jmg.3.1.17 |
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The 45XO/46XY mosaic intersex syndrome. W P Jackson, M Hoffman, and H Makda J Med Genet 1966; 3: 23-32. doi:10.1136/jmg.3.1.23 |
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ABO blood groups and cirrhosis of the liver. A J Zuckerman J Med Genet 1966; 3: 33-34. doi:10.1136/jmg.3.1.33 |
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Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia. G R Fraser, P Grunwald, and G Stamatoyannopoulos J Med Genet 1966; 3: 35-41. doi:10.1136/jmg.3.1.35 |
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Bimodal distribution of erythrocytes in heterozygotes for strong Mediterranean glucose-6-phosphate dehydrogenase deficiency. E Sartori, F Panizon, and F Zacchello J Med Genet 1966; 3: 42-46. doi:10.1136/jmg.3.1.42 |
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Turner's syndrome: further demonstration of the presence of specific cognitional deficiencies. J Money and D Alexander J Med Genet 1966; 3: 47-48. doi:10.1136/jmg.3.1.47 |
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Incidence of congenital pyloric stenosis in Malta. E A Cachia and F F Fenech J Med Genet 1966; 3: 49-50. doi:10.1136/jmg.3.1.49 |
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Gonadal dysgenesis and ulcerative colitis. A case report with clinical, cytogenetic, and post-mortem studies. E D Williams, E Engel, P D Taft, and A P Forbes J Med Genet 1966; 3: 51-55. doi:10.1136/jmg.3.1.51 |
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Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome. H B Marsden, R I Mackay, A Murray, and H E Ward J Med Genet 1966; 3: 56-58. doi:10.1136/jmg.3.1.56 |
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Congenital anomalies due to transmission of a chromosome translocation. J E Gray, J A Dartnall, R D Creery, and J Croudace J Med Genet 1966; 3: 59-61. doi:10.1136/jmg.3.1.59 |
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A family showing transmission of a translocation between a 6-12 chromosome and a 21-22 chromosome. J E Gray, J A Dartnall, and B G Macnamara J Med Genet 1966; 3: 62-65. doi:10.1136/jmg.3.1.62 |
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Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome. J H Turner, L W Bass, and S Kaplan J Med Genet 1966; 3: 66-69. doi:10.1136/jmg.3.1.66 |
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Detection of chromosomal mosaicism by computer methods. J F Jackson and P E Pulley J Med Genet 1966; 3: 70-73. doi:10.1136/jmg.3.1.70 |
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Chromosome preparation from leucocyte culture. A simplified method for collecting samples by post. J M Anders, E C Moores, and R Emanuel J Med Genet 1966; 3: 74-75. doi:10.1136/jmg.3.1.74 |
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