J Med Genet -- Table of Contents (12 [2])

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June 1975 (Volume 12, Number 2). [Index by author]

		Book Reviews Research Article

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Book Reviews

Treatment of Parkinsonism—The Role of Dopa Decarboxulase Inhibitors.
David L. Stevens
J Med Genet 1975; 12: 213. doi:10.1136/jmg.12.2.213 [PDF] [Request Permissions]

The XYY Syndrome and Klinefelter's Syndrome
M. D. Casey
J Med Genet 1975; 12: 213-214. doi:10.1136/jmg.12.2.213-a [PDF] [Request Permissions]

Birth Defects
Sarah Bundey
J Med Genet 1975; 12: 214. doi:10.1136/jmg.12.2.214 [PDF] [Request Permissions]

The Genetics of Locomotor Disorders
Rodney Harris
J Med Genet 1975; 12: 214. doi:10.1136/jmg.12.2.214-a [PDF] [Request Permissions]

Human Gene Mapping
J. H. Edwards
J Med Genet 1975; 12: 214-215. doi:10.1136/jmg.12.2.214-b [PDF] [Request Permissions]

Nucleus and Cytoplasm, 3rd ed
Susan Povey
J Med Genet 1975; 12: 215. doi:10.1136/jmg.12.2.215 [PDF] [Request Permissions]

Methods in Human Cytogenetics
Karin Buckton
J Med Genet 1975; 12: 215. doi:10.1136/jmg.12.2.215-a [PDF] [Request Permissions]

Biomathematics, vol. 5—The Genetic Structure of Populations.
Charles Smith
J Med Genet 1975; 12: 215-216. doi:10.1136/jmg.12.2.215-b [PDF] [Request Permissions]

Einführung in die Immonogenetik
G. M. Taylor
J Med Genet 1975; 12: 216. doi:10.1136/jmg.12.2.216 [PDF] [Request Permissions]

Psychiatrie. Vol. 8. Die Erblichen Myoklonisch-Epileptische-Dementiellen Kernsyndrome.
R. T. C. Pratt
J Med Genet 1975; 12: 216. doi:10.1136/jmg.12.2.216-a [PDF] [Request Permissions]

Research Article

The mechanism of genetic predisposition in congenital dislocation of the hip.
A Czeizel, G Tusnády, G Vaczó, and T Vizkelety
J Med Genet 1975; 12: 121-124. doi:10.1136/jmg.12.2.121 [Abstract] [PDF] [Request Permissions]

Two family studies on congenital dislocation of the hip after early orthopaedic screening Hungary.
A Czeizel, J Szentpétery, G Tusnády, and T Vizkelety
J Med Genet 1975; 12: 125-130. doi:10.1136/jmg.12.2.125 [Abstract] [PDF] [Request Permissions]

The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.
R Skinner, A E Emery, A J Anderson, and C Foxall
J Med Genet 1975; 12: 131-134. doi:10.1136/jmg.12.2.131 [PDF] [Request Permissions]

Amniotic fluid macrophages and the antenatal diagnosis of anencephaly and spina bifida.
G R Sutherland, D J Brock, and J B Scrimgeour
J Med Genet 1975; 12: 135-137. doi:10.1136/jmg.12.2.135 [Abstract] [PDF] [Request Permissions]

Alpha-feto-protein during development and in disease.
A Adinolfi, M Adinolfi, and Lessof
J Med Genet 1975; 12: 138-151. doi:10.1136/jmg.12.2.138 [Abstract] [PDF] [Request Permissions]

Population studies on Gilbert's syndrome.
D Owens and J Evans
J Med Genet 1975; 12: 152-156. doi:10.1136/jmg.12.2.152 [Abstract] [PDF] [Request Permissions]

Carbohydrate metabolism in dystrophia myotonica.
A G Cudworth and B A Walker
J Med Genet 1975; 12: 157-161. doi:10.1136/jmg.12.2.157 [Abstract] [PDF] [Request Permissions]

Genetical components of physiological tremor.
P J Tyrer and J Kasriel
J Med Genet 1975; 12: 162-164. doi:10.1136/jmg.12.2.162 [Abstract] [PDF] [Request Permissions]

Homozygous beta thalassaemia in Liberia.
M C Willcox, D J Weatherall, and J B Clegg
J Med Genet 1975; 12: 165-173. doi:10.1136/jmg.12.2.165 [Abstract] [PDF] [Request Permissions]

Cell membrane receptors for serological reagents.
G W Bird
J Med Genet 1975; 12: 174-184. doi:10.1136/jmg.12.2.174 [PDF] [Request Permissions]

Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy.
P Saldaña-Garcia
J Med Genet 1975; 12: 185-192. doi:10.1136/jmg.12.2.185 [Abstract] [PDF] [Request Permissions]

Trisomy 22. Two new cases and delineation of the phenotype.
V B Penchaszadeh and R Coco
J Med Genet 1975; 12: 193-199. doi:10.1136/jmg.12.2.193 [Abstract] [PDF] [Request Permissions]

Familial trisomy 7 mosaicism.
L E DeBault and K A Halmi
J Med Genet 1975; 12: 200-203. doi:10.1136/jmg.12.2.200 [Abstract] [PDF] [Request Permissions]

A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)].
C Kempen
J Med Genet 1975; 12: 204-207. doi:10.1136/jmg.12.2.204 [Abstract] [PDF] [Request Permissions]

A mentally retarded child with a translocation involving chromosomes 12 and 19.
T W Histinx, F J Gabreëls, F J Rutten, I I Korten, J M Scheres, and E M Joosten
J Med Genet 1975; 12: 207-210. doi:10.1136/jmg.12.2.207 [Abstract] [PDF] [Request Permissions]

Dicentric Y chromosome in mixed gonadal dysgenesis.
A Hayek and E Yunis
J Med Genet 1975; 12: 210-212. doi:10.1136/jmg.12.2.210 [Abstract] [PDF] [Request Permissions]

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	Treatment of Parkinsonism—The Role of Dopa Decarboxulase Inhibitors. David L. Stevens J Med Genet 1975; 12: 213. doi:10.1136/jmg.12.2.213 [PDF] [Request Permissions]

	The XYY Syndrome and Klinefelter's Syndrome M. D. Casey J Med Genet 1975; 12: 213-214. doi:10.1136/jmg.12.2.213-a [PDF] [Request Permissions]

	Birth Defects Sarah Bundey J Med Genet 1975; 12: 214. doi:10.1136/jmg.12.2.214 [PDF] [Request Permissions]

	The Genetics of Locomotor Disorders Rodney Harris J Med Genet 1975; 12: 214. doi:10.1136/jmg.12.2.214-a [PDF] [Request Permissions]

	Human Gene Mapping J. H. Edwards J Med Genet 1975; 12: 214-215. doi:10.1136/jmg.12.2.214-b [PDF] [Request Permissions]

	Nucleus and Cytoplasm, 3rd ed Susan Povey J Med Genet 1975; 12: 215. doi:10.1136/jmg.12.2.215 [PDF] [Request Permissions]

	Methods in Human Cytogenetics Karin Buckton J Med Genet 1975; 12: 215. doi:10.1136/jmg.12.2.215-a [PDF] [Request Permissions]

	Biomathematics, vol. 5—The Genetic Structure of Populations. Charles Smith J Med Genet 1975; 12: 215-216. doi:10.1136/jmg.12.2.215-b [PDF] [Request Permissions]

	Einführung in die Immonogenetik G. M. Taylor J Med Genet 1975; 12: 216. doi:10.1136/jmg.12.2.216 [PDF] [Request Permissions]

	Psychiatrie. Vol. 8. Die Erblichen Myoklonisch-Epileptische-Dementiellen Kernsyndrome. R. T. C. Pratt J Med Genet 1975; 12: 216. doi:10.1136/jmg.12.2.216-a [PDF] [Request Permissions]

	The mechanism of genetic predisposition in congenital dislocation of the hip. A Czeizel, G Tusnády, G Vaczó, and T Vizkelety J Med Genet 1975; 12: 121-124. doi:10.1136/jmg.12.2.121 [Abstract] [PDF] [Request Permissions]

	Two family studies on congenital dislocation of the hip after early orthopaedic screening Hungary. A Czeizel, J Szentpétery, G Tusnády, and T Vizkelety J Med Genet 1975; 12: 125-130. doi:10.1136/jmg.12.2.125 [Abstract] [PDF] [Request Permissions]

	The detection of carriers of benign (Becker-type) X-linked muscular dystrophy. R Skinner, A E Emery, A J Anderson, and C Foxall J Med Genet 1975; 12: 131-134. doi:10.1136/jmg.12.2.131 [PDF] [Request Permissions]

	Amniotic fluid macrophages and the antenatal diagnosis of anencephaly and spina bifida. G R Sutherland, D J Brock, and J B Scrimgeour J Med Genet 1975; 12: 135-137. doi:10.1136/jmg.12.2.135 [Abstract] [PDF] [Request Permissions]

	Alpha-feto-protein during development and in disease. A Adinolfi, M Adinolfi, and Lessof J Med Genet 1975; 12: 138-151. doi:10.1136/jmg.12.2.138 [Abstract] [PDF] [Request Permissions]

	Population studies on Gilbert's syndrome. D Owens and J Evans J Med Genet 1975; 12: 152-156. doi:10.1136/jmg.12.2.152 [Abstract] [PDF] [Request Permissions]

	Carbohydrate metabolism in dystrophia myotonica. A G Cudworth and B A Walker J Med Genet 1975; 12: 157-161. doi:10.1136/jmg.12.2.157 [Abstract] [PDF] [Request Permissions]

	Genetical components of physiological tremor. P J Tyrer and J Kasriel J Med Genet 1975; 12: 162-164. doi:10.1136/jmg.12.2.162 [Abstract] [PDF] [Request Permissions]

	Homozygous beta thalassaemia in Liberia. M C Willcox, D J Weatherall, and J B Clegg J Med Genet 1975; 12: 165-173. doi:10.1136/jmg.12.2.165 [Abstract] [PDF] [Request Permissions]

	Cell membrane receptors for serological reagents. G W Bird J Med Genet 1975; 12: 174-184. doi:10.1136/jmg.12.2.174 [PDF] [Request Permissions]

	Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy. P Saldaña-Garcia J Med Genet 1975; 12: 185-192. doi:10.1136/jmg.12.2.185 [Abstract] [PDF] [Request Permissions]

	Trisomy 22. Two new cases and delineation of the phenotype. V B Penchaszadeh and R Coco J Med Genet 1975; 12: 193-199. doi:10.1136/jmg.12.2.193 [Abstract] [PDF] [Request Permissions]

	Familial trisomy 7 mosaicism. L E DeBault and K A Halmi J Med Genet 1975; 12: 200-203. doi:10.1136/jmg.12.2.200 [Abstract] [PDF] [Request Permissions]

	A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)]. C Kempen J Med Genet 1975; 12: 204-207. doi:10.1136/jmg.12.2.204 [Abstract] [PDF] [Request Permissions]

	A mentally retarded child with a translocation involving chromosomes 12 and 19. T W Histinx, F J Gabreëls, F J Rutten, I I Korten, J M Scheres, and E M Joosten J Med Genet 1975; 12: 207-210. doi:10.1136/jmg.12.2.207 [Abstract] [PDF] [Request Permissions]

	Dicentric Y chromosome in mixed gonadal dysgenesis. A Hayek and E Yunis J Med Genet 1975; 12: 210-212. doi:10.1136/jmg.12.2.210 [Abstract] [PDF] [Request Permissions]