Only Table of Contents and PDFs available for this issue |
||
 |
||
Other Issues:
|
||
| March 1970 (Volume 7, Number 1). [Index by author] | ||
|
||
|
|
Book Review
Research Article
|
|
||
Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
|
Humangenetik. Ein kurzes Handbuch in fünf Bänden Arnold Sorsby J Med Genet 1970; 7: 101. doi:10.1136/jmg.7.1.101 |
|
|
Progress in Human Behaviour Genetics: Recent Reports on Genetic Syndromes, Twin Studies, and Statistical Advances H. J. Eysenck J Med Genet 1970; 7: 101. doi:10.1136/jmg.7.1.101-a |
|
|
Genetics and Counseling in Medical Practice Alan E. H. Emery J Med Genet 1970; 7: 102. doi:10.1136/jmg.7.1.102 |
|
|
Atlas of Mental Retardation Syndromes. Visual Diagnosis of Facies and Physical Findings L. T. Hilliard J Med Genet 1970; 7: 102. doi:10.1136/jmg.7.1.102-a |
|
|
The Future of the Brain Sciences. Proceedings of a Conference held at the New York Academy of Medicine, May 2-4, 1968 Valerie Cowie J Med Genet 1970; 7: 102-103. doi:10.1136/jmg.7.1.102-b |
|
|
Some Inherited Disorders of Brain and Muscle. Proceedings of the Fifth Symposium of the Society for the Study of Inborn Errors of Metabolism Arnold Sorsby J Med Genet 1970; 7: 103. doi:10.1136/jmg.7.1.103 |
|
|
Chromosomale Aberrationen und Psyche Ursula Mittwoch J Med Genet 1970; 7: 103. doi:10.1136/jmg.7.1.103-a |
|
|
Diagnosis and Treatment of Fetal Disorders J. S. Scott J Med Genet 1970; 7: 103-104. doi:10.1136/jmg.7.1.103-b |
|
|
Modern Biology J Med Genet 1970; 7: 104. doi:10.1136/jmg.7.1.104 |
|
|
Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome. F Hecht, D L Jones, M Delay, and H Klevit J Med Genet 1970; 7: 1-4. doi:10.1136/jmg.7.1.1 |
|
|
Genetic factors influencing human serum trehalase activity. L C Eze, M C Tweedie, and D A Evans J Med Genet 1970; 7: 5-10. doi:10.1136/jmg.7.1.5 |
|
|
Absent IgA and deletions of chromosome 18. J M Stewart, S Go, E Ellis, and A Robinson J Med Genet 1970; 7: 11-19. doi:10.1136/jmg.7.1.11 |
|
|
Affected parent and age of onset in Huntington's chorea. M B Jones and C R Phillips J Med Genet 1970; 7: 20-21. doi:10.1136/jmg.7.1.20 |
|
|
Severe achondroplasia: demonstration of probable heterogeneity within this clinical syndrome. D C Wallace, L A Exton, D A Pritchard, Y Leung, and R A Cooke J Med Genet 1970; 7: 22-26. doi:10.1136/jmg.7.1.22 |
|
|
Congenital adrenal hypoplasia--an X-linked disease. L Weiss and R C Mellinger J Med Genet 1970; 7: 27-32. doi:10.1136/jmg.7.1.27 |
|
|
A deleted B chromosome in a mosaic mother and her cri du chat progeny. J Philip, N J Brandt, B Friis-Hansen, M Mikkelsen, and I Tygstrup J Med Genet 1970; 7: 33-36. doi:10.1136/jmg.7.1.33 |
|
|
A family with a large Y chromosome. O S el-Alfi J Med Genet 1970; 7: 37-40. doi:10.1136/jmg.7.1.37 |
|
|
Huntington's chorea. Report of a chinese family in Singapore. C H Tay J Med Genet 1970; 7: 41-43. doi:10.1136/jmg.7.1.41 |
|
|
Prevalence of abnormal haemoglobins in pulmonary tuberculosis in three different ethnic groups. N Saha J Med Genet 1970; 7: 44-46. doi:10.1136/jmg.7.1.44 |
|
|
Thalassaemia intermedia: a genetic study in 11 patients. M Aksoy J Med Genet 1970; 7: 47-51. doi:10.1136/jmg.7.1.47 |
|
|
ABO and Rh blood groups in relation to marital status and childlessness in blood donors. T M Allan J Med Genet 1970; 7: 52-55. doi:10.1136/jmg.7.1.52 |
|
|
ABO blood groups, haemoglobin genotypes, and loiasis. E O Ogunba J Med Genet 1970; 7: 56-58. doi:10.1136/jmg.7.1.56 |
|
|
Inherited pericentric inversion of a human Y chromosome in trisomic Down's syndrome. R S Sparkes, H M Muller, and I C Veomett J Med Genet 1970; 7: 59-62. doi:10.1136/jmg.7.1.59 |
|
|
Achondroplasia and Down's syndrome. A Sommer and A P Eaton J Med Genet 1970; 7: 63-66. doi:10.1136/jmg.7.1.63 |
|
|
Down's syndrome and acute leukaemia: a cytogenetic study. J G Buchanan and D M Becroft J Med Genet 1970; 7: 67-69. doi:10.1136/jmg.7.1.67 |
|
|
Trisomy E and T-E fistula. A Sommer and J L Grosfeld J Med Genet 1970; 7: 70-74. doi:10.1136/jmg.7.1.70 |
|
|
New human double trisomy or tetrasomy. R K Dhadial J Med Genet 1970; 7: 75-76. doi:10.1136/jmg.7.1.75 |
|
|
A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-). G J Bargman, R L Neu, H O Powers, and L I Gardner J Med Genet 1970; 7: 77-80. doi:10.1136/jmg.7.1.77 |
|
|
t(2q-; Dq+) in a mentally retarded female child. B C Davison, J Bedford, and W Dunn J Med Genet 1970; 7: 81-82. doi:10.1136/jmg.7.1.81 |
|
|
A female with the 48,XXXX karyotype. M I Berkeley and M J Faed J Med Genet 1970; 7: 83-85. doi:10.1136/jmg.7.1.83 |
|
|
Median facial cleft associated with ring E chromosome. K W Dumars, L G Carnahan, and R V Barrett J Med Genet 1970; 7: 86-90. doi:10.1136/jmg.7.1.86 |
|
|
Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum. P Fischer, E Golob, F Friedrich, E Kunze-Mühl, W Doleschel, and H Aichmair J Med Genet 1970; 7: 91-98. doi:10.1136/jmg.7.1.91 |
|
|
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosome. G J Bargman, R L Neu, H O Powers, and L I Gardner J Med Genet 1970; 7: 99-100. doi:10.1136/jmg.7.1.99 |
|
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
