J Med Genet -- Table of Contents (16 [3])

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June 1979 (Volume 16, Number 3). [Index by author]

		Articles Editorials Miscellaneous Articles Book Reviews Research Article

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Articles

A family study of renal agenesis
C. O. Carter, Kathleen Evans, and G. Pescia
J Med Genet 1979; 16: 176-188. doi:10.1136/jmg.16.3.176 [Abstract] [PDF] [Request Permissions]

Editorials

Guidelines for cytogenetic case reports
D. G. Harnden
J Med Genet 1979; 16: 165. doi:10.1136/jmg.16.3.165 [PDF] [Request Permissions]

Miscellaneous

Errata
J Med Genet 1979; 16: 237. doi:10.1136/jmg.16.3.237 [PDF] [Request Permissions]

Articles

A family study of renal agenesis
C. O. Carter, Kathleen Evans, and G. Pescia
J Med Genet 1979; 16: 176-188. doi:10.1136/jmg.16.3.176 [Abstract] [PDF] [Request Permissions]

Book Reviews

Medical Genetic Studies of the Amish. Selected Papers
P. S. Harper
J Med Genet 1979; 16: 238. doi:10.1136/jmg.16.3.238 [PDF] [Request Permissions]

British Medical Bulletin: The HLA System
R. Harris
J Med Genet 1979; 16: 238-239. doi:10.1136/jmg.16.3.238-a [PDF] [Request Permissions]

Basic Immunogenetics 2nd Edition
R. Harris
J Med Genet 1979; 16: 239. doi:10.1136/jmg.16.3.239 [PDF] [Request Permissions]

The Genetics of Aging
J. H. Edwards
J Med Genet 1979; 16: 239-241. doi:10.1136/jmg.16.3.239-a [PDF] [Request Permissions]

Blood Groups and Diseases. A Study of Associations of Diseases with Blood Groups and Other Polymorphisms. Oxford Monographs on Medical Genetics
Marcus E. Pembrey
J Med Genet 1979; 16: 241-242. doi:10.1136/jmg.16.3.241 [PDF] [Request Permissions]

Inherited Disorders of the Skeleton
N. R. Dennis
J Med Genet 1979; 16: 242. doi:10.1136/jmg.16.3.242 [PDF] [Request Permissions]

The Study of Man. An Introduction to Human Biology 2nd Edition
D. F. Roberts
J Med Genet 1979; 16: 242-243. doi:10.1136/jmg.16.3.242-a [PDF] [Request Permissions]

Textbook of Human Genetics 2nd ed
A. E. H. Emery
J Med Genet 1979; 16: 243-244. doi:10.1136/jmg.16.3.243 [PDF] [Request Permissions]

The Eukaryotic Chromosome
Marina Seabright
J Med Genet 1979; 16: 244. doi:10.1136/jmg.16.3.244 [PDF] [Request Permissions]

Research Article

Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems.
P E Polani, E Alberman, B J Alexander, P F Benson, A C Berry, S Blunt, M G Daker, A H Fensom, D M Garrett, V M McGuire, J A Roberts, M J Seller, and J D Singer
J Med Genet 1979; 16: 166-175. doi:10.1136/jmg.16.3.166 [Abstract] [PDF] [Request Permissions]

Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.
A G Whitelaw, P A Rogers, D A Hopkinson, H Gordon, P M Emerson, J H Darley, C Reid, and M A Crawfurd
J Med Genet 1979; 16: 189-196. doi:10.1136/jmg.16.3.189 [Abstract] [PDF] [Request Permissions]

Inherited anaemias in the Greek community of Cape Town.
R P Bonafede, M C Botha, and P Beighton
J Med Genet 1979; 16: 197-200. doi:10.1136/jmg.16.3.197 [Abstract] [PDF] [Request Permissions]

Hepatitis--Bs antigen in an isolated Indian population of southern Venezuela: a family study.
A Soyano, Z Layrisse, M Layrisse, and J V Neel
J Med Genet 1979; 16: 201-205. doi:10.1136/jmg.16.3.201 [Abstract] [PDF] [Request Permissions]

Studies in mice on the mutagenicity of two contraceptive drugs.
M E Wallace, F M Badr, and R S Badr
J Med Genet 1979; 16: 206-209. doi:10.1136/jmg.16.3.206 [Abstract] [PDF] [Request Permissions]

May spina bifida result from an X-linked defect in a selective abortion mechanism?
J Burn and D Gibbens
J Med Genet 1979; 16: 210-214. doi:10.1136/jmg.16.3.210 [Abstract] [PDF] [Request Permissions]

Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1.
H N Bass and R S Sparkes
J Med Genet 1979; 16: 215-218. doi:10.1136/jmg.16.3.215 [Abstract] [PDF] [Request Permissions]

No increased chromosome breakage in three Bloom's syndrome heterozygotes.
E M Kuhn and E Therman
J Med Genet 1979; 16: 219-222. doi:10.1136/jmg.16.3.219 [Abstract] [PDF] [Request Permissions]

X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.
G Filippi, A Rinaldi, G Crisponi, G L Daniels, and M Siniscalco
J Med Genet 1979; 16: 223-224. doi:10.1136/jmg.16.3.223 [Abstract] [PDF] [Request Permissions]

Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.
A Rinaldi, N Archidiacono, M Rocchi, and G Filippi
J Med Genet 1979; 16: 225-226. doi:10.1136/jmg.16.3.225 [Abstract] [PDF] [Request Permissions]

Normal phenotype and partial trisomy for the G positive region of chromosome 21.
A Daniel
J Med Genet 1979; 16: 227-229. doi:10.1136/jmg.16.3.227 [Abstract] [PDF] [Request Permissions]

Trisomy 20p from maternal t(3;20) translocation.
N Archidiacono, D Tecilazich, G Tonini, M Rocchi, and G Filippi
J Med Genet 1979; 16: 229-232. doi:10.1136/jmg.16.3.229 [Abstract] [PDF] [Request Permissions]

Triple mosaicism 45,XY,--18/46, XY/47,XY,+18.
M Frydman, F Shabtai, Y Barak, I Halbrecht, and E Elian
J Med Genet 1979; 16: 232-234. doi:10.1136/jmg.16.3.232 [Abstract] [PDF] [Request Permissions]

The Prader-Willi syndrome with a 15/3 translocation.
M Kucerová, M Straková, and Z Polívková
J Med Genet 1979; 16: 234-235. doi:10.1136/jmg.16.3.234 [Abstract] [PDF] [Request Permissions]

Hereditary brachydactyly with nail dysplasia.
G D Schott
J Med Genet 1979; 16: 236. doi:10.1136/jmg.16.3.236 [PDF] [Request Permissions]

The Rieger syndrome.
R J Jorgenson, F E Yoder, and L S Levin
J Med Genet 1979; 16: 236-237. doi:10.1136/jmg.16.3.236-a [PDF] [Request Permissions]

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	A family study of renal agenesis C. O. Carter, Kathleen Evans, and G. Pescia J Med Genet 1979; 16: 176-188. doi:10.1136/jmg.16.3.176 [Abstract] [PDF] [Request Permissions]

	Guidelines for cytogenetic case reports D. G. Harnden J Med Genet 1979; 16: 165. doi:10.1136/jmg.16.3.165 [PDF] [Request Permissions]

	Errata J Med Genet 1979; 16: 237. doi:10.1136/jmg.16.3.237 [PDF] [Request Permissions]

	Medical Genetic Studies of the Amish. Selected Papers P. S. Harper J Med Genet 1979; 16: 238. doi:10.1136/jmg.16.3.238 [PDF] [Request Permissions]

	British Medical Bulletin: The HLA System R. Harris J Med Genet 1979; 16: 238-239. doi:10.1136/jmg.16.3.238-a [PDF] [Request Permissions]

	Basic Immunogenetics 2nd Edition R. Harris J Med Genet 1979; 16: 239. doi:10.1136/jmg.16.3.239 [PDF] [Request Permissions]

	The Genetics of Aging J. H. Edwards J Med Genet 1979; 16: 239-241. doi:10.1136/jmg.16.3.239-a [PDF] [Request Permissions]

	Blood Groups and Diseases. A Study of Associations of Diseases with Blood Groups and Other Polymorphisms. Oxford Monographs on Medical Genetics Marcus E. Pembrey J Med Genet 1979; 16: 241-242. doi:10.1136/jmg.16.3.241 [PDF] [Request Permissions]

	Inherited Disorders of the Skeleton N. R. Dennis J Med Genet 1979; 16: 242. doi:10.1136/jmg.16.3.242 [PDF] [Request Permissions]

	The Study of Man. An Introduction to Human Biology 2nd Edition D. F. Roberts J Med Genet 1979; 16: 242-243. doi:10.1136/jmg.16.3.242-a [PDF] [Request Permissions]

	Textbook of Human Genetics 2nd ed A. E. H. Emery J Med Genet 1979; 16: 243-244. doi:10.1136/jmg.16.3.243 [PDF] [Request Permissions]

	The Eukaryotic Chromosome Marina Seabright J Med Genet 1979; 16: 244. doi:10.1136/jmg.16.3.244 [PDF] [Request Permissions]

	Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems. P E Polani, E Alberman, B J Alexander, P F Benson, A C Berry, S Blunt, M G Daker, A H Fensom, D M Garrett, V M McGuire, J A Roberts, M J Seller, and J D Singer J Med Genet 1979; 16: 166-175. doi:10.1136/jmg.16.3.166 [Abstract] [PDF] [Request Permissions]

	Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis. A G Whitelaw, P A Rogers, D A Hopkinson, H Gordon, P M Emerson, J H Darley, C Reid, and M A Crawfurd J Med Genet 1979; 16: 189-196. doi:10.1136/jmg.16.3.189 [Abstract] [PDF] [Request Permissions]

	Inherited anaemias in the Greek community of Cape Town. R P Bonafede, M C Botha, and P Beighton J Med Genet 1979; 16: 197-200. doi:10.1136/jmg.16.3.197 [Abstract] [PDF] [Request Permissions]

	Hepatitis--Bs antigen in an isolated Indian population of southern Venezuela: a family study. A Soyano, Z Layrisse, M Layrisse, and J V Neel J Med Genet 1979; 16: 201-205. doi:10.1136/jmg.16.3.201 [Abstract] [PDF] [Request Permissions]

	Studies in mice on the mutagenicity of two contraceptive drugs. M E Wallace, F M Badr, and R S Badr J Med Genet 1979; 16: 206-209. doi:10.1136/jmg.16.3.206 [Abstract] [PDF] [Request Permissions]

	May spina bifida result from an X-linked defect in a selective abortion mechanism? J Burn and D Gibbens J Med Genet 1979; 16: 210-214. doi:10.1136/jmg.16.3.210 [Abstract] [PDF] [Request Permissions]

	Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1. H N Bass and R S Sparkes J Med Genet 1979; 16: 215-218. doi:10.1136/jmg.16.3.215 [Abstract] [PDF] [Request Permissions]

	No increased chromosome breakage in three Bloom's syndrome heterozygotes. E M Kuhn and E Therman J Med Genet 1979; 16: 219-222. doi:10.1136/jmg.16.3.219 [Abstract] [PDF] [Request Permissions]

	X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency. G Filippi, A Rinaldi, G Crisponi, G L Daniels, and M Siniscalco J Med Genet 1979; 16: 223-224. doi:10.1136/jmg.16.3.223 [Abstract] [PDF] [Request Permissions]

	Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis. A Rinaldi, N Archidiacono, M Rocchi, and G Filippi J Med Genet 1979; 16: 225-226. doi:10.1136/jmg.16.3.225 [Abstract] [PDF] [Request Permissions]

	Normal phenotype and partial trisomy for the G positive region of chromosome 21. A Daniel J Med Genet 1979; 16: 227-229. doi:10.1136/jmg.16.3.227 [Abstract] [PDF] [Request Permissions]

	Trisomy 20p from maternal t(3;20) translocation. N Archidiacono, D Tecilazich, G Tonini, M Rocchi, and G Filippi J Med Genet 1979; 16: 229-232. doi:10.1136/jmg.16.3.229 [Abstract] [PDF] [Request Permissions]

	Triple mosaicism 45,XY,--18/46, XY/47,XY,+18. M Frydman, F Shabtai, Y Barak, I Halbrecht, and E Elian J Med Genet 1979; 16: 232-234. doi:10.1136/jmg.16.3.232 [Abstract] [PDF] [Request Permissions]

	The Prader-Willi syndrome with a 15/3 translocation. M Kucerová, M Straková, and Z Polívková J Med Genet 1979; 16: 234-235. doi:10.1136/jmg.16.3.234 [Abstract] [PDF] [Request Permissions]

	Hereditary brachydactyly with nail dysplasia. G D Schott J Med Genet 1979; 16: 236. doi:10.1136/jmg.16.3.236 [PDF] [Request Permissions]

	The Rieger syndrome. R J Jorgenson, F E Yoder, and L S Levin J Med Genet 1979; 16: 236-237. doi:10.1136/jmg.16.3.236-a [PDF] [Request Permissions]