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| June 1966 (Volume 3, Number 2). [Index by author] | ||
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Book Reviews
Research Article
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Table of Contents (PDF) | Cover (PDF)
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British Medical Bulletin H. Kalmus J Med Genet 1966; 3: 157. doi:10.1136/jmg.3.2.157 |
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Genetic Polymorphism. (All Souls Studies V.) H. Kalmus J Med Genet 1966; 3: 157. doi:10.1136/jmg.3.2.157-a |
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The Early Conceptus, Normal and Abnormal. Papers and Discussions Presented at a Symposium held at Queen's College, Dundee, September 17th, 18th, and 19th, 1964 J. H. Edwards J Med Genet 1966; 3: 157. doi:10.1136/jmg.3.2.157-b |
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Vergleichende Untersuchungen über die Häufigkeit angeborener menschlicher Missbildungen J. H. Edwards J Med Genet 1966; 3: 158. doi:10.1136/jmg.3.2.158 |
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Genetics of the Norway Rat Arnold Sorsby J Med Genet 1966; 3: 158. doi:10.1136/jmg.3.2.158-a |
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Teach Yourself Genetics Arnold Sorsby J Med Genet 1966; 3: 158. doi:10.1136/jmg.3.2.158-b |
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Congenital asymmetry. A W Johnston and L S Penrose J Med Genet 1966; 3: 77-85. doi:10.1136/jmg.3.2.77 |
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A family study of the late infantile and juvenile forms of metachromatic leucodystrophy. H S Schutta, R T Pratt, H Metz, K A Evans, and C O Carter J Med Genet 1966; 3: 86-91. doi:10.1136/jmg.3.2.86 |
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Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy. A E Emery J Med Genet 1966; 3: 92-95. doi:10.1136/jmg.3.2.92 |
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Chromosome studies in familial leukaemia. P H Fitzgerald, P E Crossen, A C Adams, C V Sharman, and F W Gunz J Med Genet 1966; 3: 96-100. doi:10.1136/jmg.3.2.96 |
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ABO and rhesus blood group distribution among patients attending veneral diseases clinics. C B Schofield J Med Genet 1966; 3: 101-103. doi:10.1136/jmg.3.2.101 |
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Hereditary contractures of the fingers (camptodactyly). J P Welch and S A Temtamy J Med Genet 1966; 3: 104-113. doi:10.1136/jmg.3.2.104 |
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Twins in sibships with Klinefelter's syndrome. J Nielsen J Med Genet 1966; 3: 114-116. doi:10.1136/jmg.3.2.114 |
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Monozygotic twins of different sex. J H Edwards, T Dent, and J Kahn J Med Genet 1966; 3: 117-123. doi:10.1136/jmg.3.2.117 |
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Turner's syndrome in monozygotic twins. I B Shine and G Corney J Med Genet 1966; 3: 124-128. doi:10.1136/jmg.3.2.124 |
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An XO-X ring X chromosome mosaicism in an individual with normal secondary sexual development. A M Bishop, C E Blank, K Simpson, and C J Dewhurst J Med Genet 1966; 3: 129-133. doi:10.1136/jmg.3.2.129 |
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An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development. L Atkins, R T Sceery, and M E Keenan J Med Genet 1966; 3: 134-138. doi:10.1136/jmg.3.2.134 |
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Klinefelter's syndrome with a presumptive deleted X chromosome. J Nielsen J Med Genet 1966; 3: 139-141. doi:10.1136/jmg.3.2.139 |
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13-15 trisomy mosiacism in a normal-looking 14-year-old retarded girl. D Stone, A S Akad, C Noyes, and E Lamson J Med Genet 1966; 3: 142-144. doi:10.1136/jmg.3.2.142 |
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Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies. C C Tucker, S C Finley, E S Tucker, and W H Finley J Med Genet 1966; 3: 145-147. doi:10.1136/jmg.3.2.145 |
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Bloch-Sulzberger Syndrome (incontinentia pigmenti). N Shotts and A E Emery J Med Genet 1966; 3: 148-152. doi:10.1136/jmg.3.2.148 |
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Epiloia (tuberous sclerosis): a report of a case with unusual tumours. J M Berg, E A Green, and M A Ridler J Med Genet 1966; 3: 153-155. doi:10.1136/jmg.3.2.153 |
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Hypertrichosis terminalis with simian characteristics. A K Ray J Med Genet 1966; 3: 156. doi:10.1136/jmg.3.2.156 |
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