Register for email alerts and news feeds:
This journal | BMJ Group
rss

Only Table of Contents and PDFs available for this issue

Other Issues: prev. next
June 1970    (Volume 7, Number 2).   [Index by author]
 Cover Image Down Book Review
Down Research Article

[Search ALL Issues]

Table of Contents (PDF) | Cover (PDF) | Administration (PDF)

Back Book Review
Grundriss der Genetik
H. Kalmus
J Med Genet 1970; 7: 189. doi:10.1136/jmg.7.2.189 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
Progress in Medical Genetics
A. E. H. Emery
J Med Genet 1970; 7: 190. doi:10.1136/jmg.7.2.190 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
Human Afflictions and Chromosome Abberations
John L. Hamerton
J Med Genet 1970; 7: 191. doi:10.1136/jmg.7.2.191 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
The Elements of Cytogenetics
John L. Hamerton
J Med Genet 1970; 7: 191. doi:10.1136/jmg.7.2.191-b [PDF] [Request Permissions]  
Endocrinopatile Genetice
Arnold Sorsby
J Med Genet 1970; 7: 191-192. doi:10.1136/jmg.7.2.191-c [PDF] [Request Permissions]  
Gene Activity in Early Development
Ursula Mittwoch
J Med Genet 1970; 7: 192. doi:10.1136/jmg.7.2.192 [PDF] [Request Permissions]  

Back Research Article
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
Dermatoglyphs in leukaemia.
J L Verbov
J Med Genet 1970; 7: 125-131. doi:10.1136/jmg.7.2.125 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
Familial hypertrichosis cubiti: hairy elbows syndrome.
P Beighton
J Med Genet 1970; 7: 158-160. doi:10.1136/jmg.7.2.158 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  
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 [PDF] [Request Permissions]  

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.

Genetics jobs

Genetics jobs