J Med Genet -- Table of Contents (18 [3])

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June 1981 (Volume 18, Number 3). [Index by author]

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Articles

Clinical Genetics Society. Abstracts of scientific papers presented on 18 and 19 September 1980 in Aberdeen
J Med Genet 1981; 18: 218-224. doi:10.1136/jmg.18.3.218 [PDF] [Request Permissions]

Book Reviews

Advances in Human Genetics
M Baraitser
J Med Genet 1981; 18: 242. doi:10.1136/jmg.18.3.242 [PDF] [Request Permissions]

Genetics
A E Harding
J Med Genet 1981; 18: 242. doi:10.1136/jmg.18.3.242-a [PDF] [Request Permissions]

Development, Growth and Ageing
D F Roberts
J Med Genet 1981; 18: 242-243. doi:10.1136/jmg.18.3.242-b [PDF] [Request Permissions]

Human Gene Mapping 5
P J L Cook
J Med Genet 1981; 18: 243. doi:10.1136/jmg.18.3.243 [PDF] [Request Permissions]

Genes and the Mind. Inheritance of Mental Illness
M Baraitser
J Med Genet 1981; 18: 243-244. doi:10.1136/jmg.18.3.243-a [PDF] [Request Permissions]

Research Article

Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.
R M Davis
J Med Genet 1981; 18: 161-195. doi:10.1136/jmg.18.3.161 [Abstract] [PDF] [Request Permissions]

Beta-Thalassaemia types in southern Sardinia.
A Cao, M Furbetta, A Ximenes, A Angius, C Rosatelli, T Tuveri, M T Scalas, A M Falchi, L Maccioni, M A Melis, and R Galanello
J Med Genet 1981; 18: 196-199. doi:10.1136/jmg.18.3.196 [Abstract] [PDF] [Request Permissions]

Huntington's disease in Tanzania.
E M Scrimgeour
J Med Genet 1981; 18: 200-203. doi:10.1136/jmg.18.3.200 [Abstract] [PDF] [Request Permissions]

Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
E S Sachs and G van Waveren
J Med Genet 1981; 18: 204-208. doi:10.1136/jmg.18.3.204 [Abstract] [PDF] [Request Permissions]

Inheritance of a ring 14 chromosome.
S B Riley, K E Buckton, S G Ratcliffe, and J Syme
J Med Genet 1981; 18: 209-213. doi:10.1136/jmg.18.3.209 [Abstract] [PDF] [Request Permissions]

Ectodermal dysplasia in females and inversion of chromosome 9.
H M Fuenmayor, L Roldan-París, and H Bermúdez
J Med Genet 1981; 18: 214-217. doi:10.1136/jmg.18.3.214 [Abstract] [PDF] [Request Permissions]

Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).
J L Watt, D A Couzin, A W Johnston, V Jandial, and E S Gray
J Med Genet 1981; 18: 225-227. doi:10.1136/jmg.18.3.225 [Abstract] [PDF] [Request Permissions]

Structural aberration of the X chromosome in a patient with gonadal dysgenesis: an approach to karyotype-phenotype correlation.
M Varella-Garcia, E H Tajara, and A R Gagliardi
J Med Genet 1981; 18: 228-231. doi:10.1136/jmg.18.3.228 [Abstract] [PDF] [Request Permissions]

Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation.
P Ferrando, C San Román, S Rodriguez de Cordoba, and A Arnaiz-Villena
J Med Genet 1981; 18: 231-234. doi:10.1136/jmg.18.3.231 [Abstract] [PDF] [Request Permissions]

An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?
N J Carpenter, L G Leichtman, S Stamper, and B Say
J Med Genet 1981; 18: 234-236. doi:10.1136/jmg.18.3.234 [Abstract] [PDF] [Request Permissions]

Presentation of mucopolysaccharidosis VII (beta-glucuronidase deficiency) in infancy.
H E Hoyme, K L Jones, M C Higginbottom, and J S O'Brien
J Med Genet 1981; 18: 237-239. doi:10.1136/jmg.18.3.237 [Abstract] [PDF] [Request Permissions]

Anal atresia and the Klein-Waardenburg syndrome.
J Nutman, I Nissenkorn, I Varsano, M Mimouni, and R M Goodman
J Med Genet 1981; 18: 239-241. doi:10.1136/jmg.18.3.239 [Abstract] [PDF] [Request Permissions]

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	Clinical Genetics Society. Abstracts of scientific papers presented on 18 and 19 September 1980 in Aberdeen J Med Genet 1981; 18: 218-224. doi:10.1136/jmg.18.3.218 [PDF] [Request Permissions]

	Advances in Human Genetics M Baraitser J Med Genet 1981; 18: 242. doi:10.1136/jmg.18.3.242 [PDF] [Request Permissions]

	Genetics A E Harding J Med Genet 1981; 18: 242. doi:10.1136/jmg.18.3.242-a [PDF] [Request Permissions]

	Development, Growth and Ageing D F Roberts J Med Genet 1981; 18: 242-243. doi:10.1136/jmg.18.3.242-b [PDF] [Request Permissions]

	Human Gene Mapping 5 P J L Cook J Med Genet 1981; 18: 243. doi:10.1136/jmg.18.3.243 [PDF] [Request Permissions]

	Genes and the Mind. Inheritance of Mental Illness M Baraitser J Med Genet 1981; 18: 243-244. doi:10.1136/jmg.18.3.243-a [PDF] [Request Permissions]

	Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome. R M Davis J Med Genet 1981; 18: 161-195. doi:10.1136/jmg.18.3.161 [Abstract] [PDF] [Request Permissions]

	Beta-Thalassaemia types in southern Sardinia. A Cao, M Furbetta, A Ximenes, A Angius, C Rosatelli, T Tuveri, M T Scalas, A M Falchi, L Maccioni, M A Melis, and R Galanello J Med Genet 1981; 18: 196-199. doi:10.1136/jmg.18.3.196 [Abstract] [PDF] [Request Permissions]

	Huntington's disease in Tanzania. E M Scrimgeour J Med Genet 1981; 18: 200-203. doi:10.1136/jmg.18.3.200 [Abstract] [PDF] [Request Permissions]

	Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation. E S Sachs and G van Waveren J Med Genet 1981; 18: 204-208. doi:10.1136/jmg.18.3.204 [Abstract] [PDF] [Request Permissions]

	Inheritance of a ring 14 chromosome. S B Riley, K E Buckton, S G Ratcliffe, and J Syme J Med Genet 1981; 18: 209-213. doi:10.1136/jmg.18.3.209 [Abstract] [PDF] [Request Permissions]

	Ectodermal dysplasia in females and inversion of chromosome 9. H M Fuenmayor, L Roldan-París, and H Bermúdez J Med Genet 1981; 18: 214-217. doi:10.1136/jmg.18.3.214 [Abstract] [PDF] [Request Permissions]

	Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0). J L Watt, D A Couzin, A W Johnston, V Jandial, and E S Gray J Med Genet 1981; 18: 225-227. doi:10.1136/jmg.18.3.225 [Abstract] [PDF] [Request Permissions]

	Structural aberration of the X chromosome in a patient with gonadal dysgenesis: an approach to karyotype-phenotype correlation. M Varella-Garcia, E H Tajara, and A R Gagliardi J Med Genet 1981; 18: 228-231. doi:10.1136/jmg.18.3.228 [Abstract] [PDF] [Request Permissions]

	Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation. P Ferrando, C San Román, S Rodriguez de Cordoba, and A Arnaiz-Villena J Med Genet 1981; 18: 231-234. doi:10.1136/jmg.18.3.231 [Abstract] [PDF] [Request Permissions]

	An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome? N J Carpenter, L G Leichtman, S Stamper, and B Say J Med Genet 1981; 18: 234-236. doi:10.1136/jmg.18.3.234 [Abstract] [PDF] [Request Permissions]

	Presentation of mucopolysaccharidosis VII (beta-glucuronidase deficiency) in infancy. H E Hoyme, K L Jones, M C Higginbottom, and J S O'Brien J Med Genet 1981; 18: 237-239. doi:10.1136/jmg.18.3.237 [Abstract] [PDF] [Request Permissions]

	Anal atresia and the Klein-Waardenburg syndrome. J Nutman, I Nissenkorn, I Varsano, M Mimouni, and R M Goodman J Med Genet 1981; 18: 239-241. doi:10.1136/jmg.18.3.239 [Abstract] [PDF] [Request Permissions]