Only Table of Contents and PDFs available for this issue |
||
 |
||
Other Issues:
|
||
| December 1972 (Volume 9, Number 4). [Index by author] | ||
|
||
|
|
Book Review
Research Article
|
|
||
Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
|
Biomathematics J. H. Edwards J Med Genet 1972; 9: 485. doi:10.1136/jmg.9.4.485 |
|
|
Comparative Genetics in Monkeys, Apes and Man C. O. Carter J Med Genet 1972; 9: 485-486. doi:10.1136/jmg.9.4.485-a |
|
|
Progress in Medical Genetics, Vol. 8 Alan E. H. Emery J Med Genet 1972; 9: 486. doi:10.1136/jmg.9.4.486 |
|
|
The Role of Genetics in Mental Retardation B. W. Richards J Med Genet 1972; 9: 486-487. doi:10.1136/jmg.9.4.486-a |
|
|
Aminoacidopathies, Immunoglobinopathies, Neuro-genetics and Neuro-ophthalmology Sarah Bundey J Med Genet 1972; 9: 487. doi:10.1136/jmg.9.4.487 |
|
|
A rare blood group antigen An a (Ahonen). U Furuhjelm, H R Nevanlinna, J Gavin, and R Sanger J Med Genet 1972; 9: 385-391. doi:10.1136/jmg.9.4.385 |
|
|
The Dombrock system: linkage relations with other blood group loci. P Tippett, J Gavin, and R Sanger J Med Genet 1972; 9: 392-395. doi:10.1136/jmg.9.4.392 |
|
|
Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization. T Révész, D Schuler, B Goldschmidt, and S Elödi J Med Genet 1972; 9: 396-400. doi:10.1136/jmg.9.4.396 |
|
|
A new genetic variant of the spinal muscular atrophies in infancy. H Zellweger, E Hanhart, and H J Schneider J Med Genet 1972; 9: 401-407. doi:10.1136/jmg.9.4.401 |
|
|
Pedigrees with diabetes insipidus, diabetes mellitus, and optic atrophy. J H Sunder, T S Danowski, F M Kenny, R C Khurana, A Sun, S Nolan, and T Stephan J Med Genet 1972; 9: 408-412. doi:10.1136/jmg.9.4.408 |
|
|
Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals. H Hauksdóttir, S Halldórsson, O Jensson, M Mikkelsen, and A McDermott J Med Genet 1972; 9: 413-421. doi:10.1136/jmg.9.4.413 |
|
|
Reciprocal chromosome translocations: analysis of two mutants by interactive computer. R W Dickerson, N H Xuong, and O W Jones J Med Genet 1972; 9: 422-429. doi:10.1136/jmg.9.4.422 |
|
|
The nature and inheritance of Kirner's deformity. T J David and R L Burwood J Med Genet 1972; 9: 430-433. doi:10.1136/jmg.9.4.430 |
|
|
Erythrocyte acid phosphatase polymorphism and haemolysis. E Bottini, P Lucarelli, V Bastianon, and F Gloria J Med Genet 1972; 9: 434-435. doi:10.1136/jmg.9.4.434 |
|
|
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. P K Sukumaran, S M Merchant, M P Desai, B G Wiltshire, and H Lehmann J Med Genet 1972; 9: 436-442. doi:10.1136/jmg.9.4.436 |
|
|
Palmar dermatoglyphs in tuberous sclerosis. T J David J Med Genet 1972; 9: 443-447. doi:10.1136/jmg.9.4.443 |
|
|
The effect of absence of thumb on palmar dermatoglyphics. S B Holt J Med Genet 1972; 9: 448-450. doi:10.1136/jmg.9.4.448 |
|
|
Familial cancer of the colon and rectum. G H Dunstone and T W Knaggs J Med Genet 1972; 9: 451-456. doi:10.1136/jmg.9.4.451 |
|
|
Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family. R Schmidt, G Mundel, M Rosenblatt, and M B Katznelson J Med Genet 1972; 9: 457-461. doi:10.1136/jmg.9.4.457 |
|
|
Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography. H Müller, E M Bühler, E Signer, F Egli, and G R Stalder J Med Genet 1972; 9: 462-467. doi:10.1136/jmg.9.4.462 |
|
|
Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells. H Van den Berghe, J P Fryns, and H Verresen J Med Genet 1972; 9: 468-470. doi:10.1136/jmg.9.4.468 |
|
|
Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease. M Faed, H G Morton, and J Robertson J Med Genet 1972; 9: 470-473. doi:10.1136/jmg.9.4.470 |
|
|
Bone marrow chromosomes in Fanconi's anaemia. S R Wolman and M Swift J Med Genet 1972; 9: 473-474. doi:10.1136/jmg.9.4.473 |
|
|
Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells. M J Shahid, F P Khouri, and S K Ballas J Med Genet 1972; 9: 474-478. doi:10.1136/jmg.9.4.474 |
|
|
Down's syndrome with an atypical G-G translocation derived from familial pericentric inversion in one chromosome of the G group. S Moric-Petrovic, Z Laca, and P Kalicanin J Med Genet 1972; 9: 478-482. doi:10.1136/jmg.9.4.478 |
|
|
A new HGPRT-deficient phenotype? S Kelly, E J Hart, and L Desjardins J Med Genet 1972; 9: 482-484. doi:10.1136/jmg.9.4.482 |
|
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.
