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| June 1972 (Volume 9, Number 2). [Index by author] | ||
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Miscellaneous
Correspondence
Book Review
Research Article
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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Corrigenda J Med Genet 1972; 9: 249. doi:10.1136/jmg.9.2.249 |
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Corrigenda J Med Genet 1972; 9: 249. doi:10.1136/jmg.9.2.249-a |
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Correspondence Marcus Pembrey J Med Genet 1972; 9: 250. doi:10.1136/jmg.9.2.250 |
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The Bacteriophage Lambda S. W. Glover J Med Genet 1972; 9: 251-252. doi:10.1136/jmg.9.2.251 |
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Ecological Genetics and Evolution P. M. Sheppard J Med Genet 1972; 9: 252. doi:10.1136/jmg.9.2.252 |
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Twin heritability study of the effect of corticosteroids on intraocular pressure. J T Schwartz, F H Reuling, M Feinleib, R J Garrison, and D J Collie J Med Genet 1972; 9: 137-143. doi:10.1136/jmg.9.2.137 |
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ABO incompatibility as a cause of spontaneous abortion: evidence from abortuses. K Takano and J R Miller J Med Genet 1972; 9: 144-150. doi:10.1136/jmg.9.2.144 |
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Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S. C H Beresford, J B Clegg, and D J Weatherall J Med Genet 1972; 9: 151-153. doi:10.1136/jmg.9.2.151 |
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Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F. C Kattamis, P Lagos, A Metaxotou-Mavromati, and N Matsaniotis J Med Genet 1972; 9: 154-159. doi:10.1136/jmg.9.2.154 |
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A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family. E B Howell, A J Nelson, and O W Jones J Med Genet 1972; 9: 160-164. doi:10.1136/jmg.9.2.160 |
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Searching for XYY males through electrocardiograms. A M Vianna, O Frota-Pessoa, M F Lion, and L Decourt J Med Genet 1972; 9: 165-167. doi:10.1136/jmg.9.2.165 |
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The polymorphic acetylation of sulphapyridine in man. H Schröder and D A Evans J Med Genet 1972; 9: 168-171. doi:10.1136/jmg.9.2.168 |
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Blood enzymes in the de Lange syndrome. G F Smith, P Justice, and D Y Hsia J Med Genet 1972; 9: 172-173. doi:10.1136/jmg.9.2.172 |
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Rural-urban differentials in consanguinity. P S Rao, S G Inbaraj, and G Jesudian J Med Genet 1972; 9: 174-178. doi:10.1136/jmg.9.2.174 |
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A family study of Fallot's tetralogy. A R Boon, M B Farmer, and D F Roberts J Med Genet 1972; 9: 179-192. doi:10.1136/jmg.9.2.179 |
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Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation. S A Mirhosseini, L B Holmes, and D S Walton J Med Genet 1972; 9: 193-196. doi:10.1136/jmg.9.2.193 |
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Incidence and genetics of Legg-Perthes disease (osteochondritis deformans) in British Columbia: evidence of polygenic determination. I M Gray, R B Lowry, and D H Renwick J Med Genet 1972; 9: 197-202. doi:10.1136/jmg.9.2.197 |
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Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes. R M Goodman, M B Katznelson, and E Manor J Med Genet 1972; 9: 203-212. doi:10.1136/jmg.9.2.203 |
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Recessively inherited myotonia congenita. P S Harper and D M Johnston J Med Genet 1972; 9: 213-215. doi:10.1136/jmg.9.2.213 |
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The dominant and recessive forms of cutis laxa. P Beighton J Med Genet 1972; 9: 216-221. doi:10.1136/jmg.9.2.216 |
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Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form. C S Bartsocas and C V Papas J Med Genet 1972; 9: 222-226. doi:10.1136/jmg.9.2.222 |
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Congenital absence of the fibula and craniosynostosis in sibs. R B Lowry J Med Genet 1972; 9: 227-229. doi:10.1136/jmg.9.2.227 |
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A case of 48,XXXX female with normal intelligence. R D Blackston and A T Chen J Med Genet 1972; 9: 230-232. doi:10.1136/jmg.9.2.230 |
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A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene. R H Lindenbaum, N L Blackwell, and D J De Sa' J Med Genet 1972; 9: 232-235. doi:10.1136/jmg.9.2.232 |
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Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism. P Cooke, J A Black, and D J Curtis J Med Genet 1972; 9: 235-238. doi:10.1136/jmg.9.2.235 |
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Triple X female and a Down's syndrome offspring. J Singer, S Sachdeva, G F Smith, and D Y Hsia J Med Genet 1972; 9: 238-239. doi:10.1136/jmg.9.2.238 |
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A human ring C chromosome associated with multiple congenital abnormalities. P R De Chieri, J M Albores, A Cosín, and J M Cosín J Med Genet 1972; 9: 239-242. doi:10.1136/jmg.9.2.239 |
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Double aneuploidy (47,XX,21+-45,X) arising through simultaneous double non-disjunction. M M Cohen and R G Davidson J Med Genet 1972; 9: 242-244. doi:10.1136/jmg.9.2.242 |
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Immunological studies in congenital nephrosis. W Griswold and R M McIntosh J Med Genet 1972; 9: 245-247. doi:10.1136/jmg.9.2.245 |
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Multiple congenital defects associated with an abnormal unclassifiable karyotype. R B Surana, T M Hunt, and P E Conen J Med Genet 1972; 9: 247-249. doi:10.1136/jmg.9.2.247 |
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