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| December 1970 (Volume 7, Number 4). [Index by author] | ||
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Book Review
Research Article
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Table of Contents (PDF) | Cover (PDF) | Administration (PDF)
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Genetic Counseling. A Guide for the Practicing Physician E. M. Williamson J Med Genet 1970; 7: 426. doi:10.1136/jmg.7.4.426 |
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Éléments de Génétique Générale et Humaine R. Harris J Med Genet 1970; 7: 426. doi:10.1136/jmg.7.4.426-a |
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The Biology of Twinning in Man James Shields J Med Genet 1970; 7: 426-427. doi:10.1136/jmg.7.4.426-b |
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Evolution and the Genetics of Populations. A Treatise in Three Volumes. Volume 2: The Theory of Gene Frequencies M. G. Bulmer J Med Genet 1970; 7: 427. doi:10.1136/jmg.7.4.427 |
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Cold Spring Harbor Symposia on Quantitative Biology, Vol. XXXIV J. B. Clegg J Med Genet 1970; 7: 427. doi:10.1136/jmg.7.4.427-a |
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Animal models for bone-marrow transplantation. M H Seller J Med Genet 1970; 7: 305-309. doi:10.1136/jmg.7.4.305 |
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Genetics of immunity deficiency syndromes. H E Kay J Med Genet 1970; 7: 310-314. doi:10.1136/jmg.7.4.310 |
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A family study of neonatal and late-diagnosis congenital dislocation of the hip. R Wynne-Davies J Med Genet 1970; 7: 315-333. doi:10.1136/jmg.7.4.315 |
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Mutation rate in Duchenne type of muscular dystrophy. D Gardner-Medwin J Med Genet 1970; 7: 334-337. doi:10.1136/jmg.7.4.334 |
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Dermatoglyphs of Chinese children and Down's syndrome. J I Bryant, I Emanuel, S W Huang, R Kronmal, and J Lo J Med Genet 1970; 7: 338-344. doi:10.1136/jmg.7.4.338 |
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Comments on patients with sex chromosome aneuploidy: dermatoglyphs, parental ages, Xg a blood group. D S Borgaonkar and E Mules J Med Genet 1970; 7: 345-350. doi:10.1136/jmg.7.4.345 |
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Value of butyrylthiocholine assay for identification of cholinesterase variants. P K Das and J Liddell J Med Genet 1970; 7: 351-355. doi:10.1136/jmg.7.4.351 |
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Adenosine deaminase: racial distribution and report of a new phenotype. J C Detter, G Stamatoyannopoulos, E R Giblett, and A G Motulsky J Med Genet 1970; 7: 356-357. doi:10.1136/jmg.7.4.356 |
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Haemoglobin J in the French Canadian. S Kelly, L Desjardins, and D Juckett J Med Genet 1970; 7: 358-362. doi:10.1136/jmg.7.4.358 |
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Trisomy E (18) syndrome: clinical spectrum in 12 new cases, including chromosome autoradiography in 4. F M Weber and R S Sparkes J Med Genet 1970; 7: 363-366. doi:10.1136/jmg.7.4.363 |
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Protease inhibitor (Pi) phenotypes in chromosome aberrations. D Aarskog and M K Fagerhol J Med Genet 1970; 7: 367-370. doi:10.1136/jmg.7.4.367 |
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Satellite associations of D group chromosomes in translocation carriers. Y Nakagome and A D Bloom J Med Genet 1970; 7: 371-373. doi:10.1136/jmg.7.4.371 |
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Normal chromosomes in mucosol neuroma variant of medullary thyroid carcinoma syndrome. H Nankin, J Hydovitz, and J Sapira J Med Genet 1970; 7: 374-378. doi:10.1136/jmg.7.4.374 |
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A familial syndrome of short stature, deformities of the hands and feet, and an unusual facies. A E Emery and M M Nelson J Med Genet 1970; 7: 379-382. doi:10.1136/jmg.7.4.379 |
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Evidence of XX-XY sex chromosome mosaicism in a child with true hermaphroditism. P H Fitzgerald, L A Brehaut, F T Shannon, and H B Angus J Med Genet 1970; 7: 383-388. doi:10.1136/jmg.7.4.383 |
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A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome. J R Miller, F J Dill, M J Corey, and J M Rigg J Med Genet 1970; 7: 389-393. doi:10.1136/jmg.7.4.389 |
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A case of XX male syndrome. R Lisker, F Flores, A Cobo, and F G Rojas J Med Genet 1970; 7: 394-398. doi:10.1136/jmg.7.4.394 |
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D1 ring chromosome in newborn with peculiar face, polydactyly, imperforate anus, arrhinencephaly, and other malformations. A R Biles, Jr, T Lüers, and K Sperling J Med Genet 1970; 7: 399-401. doi:10.1136/jmg.7.4.399 |
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Possible X-autosomal translocation in a girl with gonadal dysgenesis. M J Thorburn, P A Martin, and U N Pathak J Med Genet 1970; 7: 402-406. doi:10.1136/jmg.7.4.402 |
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An extra chromosomal centric fragment in an infant with stigmata of Down's syndrome. I Subrt and H Prchlíková J Med Genet 1970; 7: 407-409. doi:10.1136/jmg.7.4.407 |
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Gonadoblastoma in a phenotypic female with 45,X-47,XYY mosaicism. M V Suñé, J V Centeno, and F M Salzano J Med Genet 1970; 7: 410-412. doi:10.1136/jmg.7.4.410 |
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Cytogenetic studies in a patient with a de novo t(Cq-;Gp+). B F Crandall, R E Carrel, G L Adams, and R S Sparkes J Med Genet 1970; 7: 413-416. doi:10.1136/jmg.7.4.413 |
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An unusual chromosomal aberration in a case of Chediak-Higashi syndrome. B Say, E Tunçbilek, B Yamak, and S Balci J Med Genet 1970; 7: 417-421. doi:10.1136/jmg.7.4.417 |
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Gargoylism in a Chinese boy. M T Tsuang, H Y Chang, and E K Yeh J Med Genet 1970; 7: 422-425. doi:10.1136/jmg.7.4.422 |
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