J Med Genet -- Table of Contents (20 [4])

Subscribe here
Activate your subscription

Home > Volume 20, Number 4

Only Abstracts and PDFs available for this issue

Other Issues:
August 1983 (Volume 20, Number 4). [Index by author]

		Articles Miscellaneous Correspondence Articles Book Reviews Research Article

Find articles in this issue containing these words: [Search ALL Issues]

Table of Contents (PDF) | Advertising (PDF) | Cover (PDF) | Administration (PDF)

To see an article, click its [Full Text] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstracts' button. To see one abstract at a time, click its [Abstract] link.

Articles

Editorial
C A Clarke
J Med Genet 1983; 20: 241-243. doi:10.1136/jmg.20.4.241 [PDF] [Request Permissions]

Abstracts of the Joint Meeting of the Clinical Genetics Society and the Royal College of Obstetricians and Gynaecologists held at the Royal College, London, on 27 October 1982
J Med Genet 1983; 20: 300-302. doi:10.1136/jmg.20.4.300 [PDF] [Request Permissions]

Miscellaneous

Correction
J Med Genet 1983; 20: 312. doi:10.1136/jmg.20.4.312 [PDF] [Request Permissions]

Correspondence

The cause(s) of neural tube defect
W H James
J Med Genet 1983; 20: 314. doi:10.1136/jmg.20.4.314 [PDF] [Request Permissions]

Book Reviews

Familial Inherited Abnormalities
A W Johnston
J Med Genet 1983; 20: 316. doi:10.1136/jmg.20.4.316 [PDF] [Request Permissions]

Histocompatibility Antigens. Structure and Function
Rodney Harris
J Med Genet 1983; 20: 316-317. doi:10.1136/jmg.20.4.316-a [PDF] [Request Permissions]

Genetic Variants and Strains of the Laboratory Mouse
M S Deol
J Med Genet 1983; 20: 317. doi:10.1136/jmg.20.4.317 [PDF] [Request Permissions]

Animal Models of Inherited Metabolic Diseases
A D Patrick
J Med Genet 1983; 20: 317. doi:10.1136/jmg.20.4.317-a [PDF] [Request Permissions]

Genetic Recombination. Understanding the Mechanisms
Kay E Davies
J Med Genet 1983; 20: 317-318. doi:10.1136/jmg.20.4.317-b [PDF] [Request Permissions]

Early Diagnosis of Fetal Defects
N R Dennis
J Med Genet 1983; 20: 318. doi:10.1136/jmg.20.4.318 [PDF] [Request Permissions]

Research Article

The teaching of human genetics in schools.
J S Fitzsimmons
J Med Genet 1983; 20: 244-248. doi:10.1136/jmg.20.4.244 [PDF] [Request Permissions]

Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences.
T O'Brien, P S Harper, K E Davies, J M Murray, M Sarfarazi, and R Williamson
J Med Genet 1983; 20: 249-251. doi:10.1136/jmg.20.4.249 [Abstract] [PDF] [Request Permissions]

The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
P S Harper, T O'Brien, J M Murray, K E Davies, P Pearson, and R Williamson
J Med Genet 1983; 20: 252-254. doi:10.1136/jmg.20.4.252 [Abstract] [PDF] [Request Permissions]

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
H M Kingston, N S Thomas, P L Pearson, M Sarfarazi, and P S Harper
J Med Genet 1983; 20: 255-258. doi:10.1136/jmg.20.4.255 [Abstract] [PDF] [Request Permissions]

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.
K E Davies, J Jackson, R Williamson, P S Harper, S Ball, M Sarfarazi, L Meredith, and G Fey
J Med Genet 1983; 20: 259-263. doi:10.1136/jmg.20.4.259 [Abstract] [PDF] [Request Permissions]

The X linked recessive form of XY gonadal dysgenesis with a high incidence of gonadal germ cell tumours: clinical and genetic studies.
J R Mann, J J Corkery, H J Fisher, A H Cameron, A Mayerová, U Wolf, A A Kennaugh, and V Woolley
J Med Genet 1983; 20: 264-270. doi:10.1136/jmg.20.4.264 [Abstract] [PDF] [Request Permissions]

Evaluation of segregation ratio in Wilson's disease.
T Saito
J Med Genet 1983; 20: 271-275. doi:10.1136/jmg.20.4.271 [Abstract] [PDF] [Request Permissions]

Thoracic-pelvic dysostosis: a 'new' autosomal dominant form.
A Bankier and D M Danks
J Med Genet 1983; 20: 276-279. doi:10.1136/jmg.20.4.276 [Abstract] [PDF] [Request Permissions]

The fragile X: a scanning electron microscope study.
C J Harrison, E M Jack, T D Allen, and R Harris
J Med Genet 1983; 20: 280-285. doi:10.1136/jmg.20.4.280 [Abstract] [PDF] [Request Permissions]

Fragile X trait in a large kindred: transmission also through normal males.
B C Van Roy, M C De Smedt, R A Raes, J E Dumon, and J G Leroy
J Med Genet 1983; 20: 286-289. doi:10.1136/jmg.20.4.286 [Abstract] [PDF] [Request Permissions]

Chiasma distribution, genetic lengths, and recombination fractions: a comparison between chromosomes 15 and 16.
N Saadallah and M Hultén
J Med Genet 1983; 20: 290-299. doi:10.1136/jmg.20.4.290 [Abstract] [PDF] [Request Permissions]

Cardiac rhabdomyomata as a marker for the antenatal detection of tuberous sclerosis.
D C Crawford, C Garrett, M Tynan, B G Neville, and L D Allan
J Med Genet 1983; 20: 303-304. doi:10.1136/jmg.20.4.303 [Abstract] [PDF] [Request Permissions]

Unusual ocular findings in an infant with cri-du-chat syndrome.
S Kitsiou-Tzeli, H D Dellagrammaticas, C B Papas, I D Ladas, and C S Bartsocas
J Med Genet 1983; 20: 304-307. doi:10.1136/jmg.20.4.304 [Abstract] [PDF] [Request Permissions]

Phenazopyridine induced methaemoglobinaemia associated with decreased activity of erythrocyte cytochrome b5 reductase.
J S Daly, D E Hultquist, and D L Rucknagel
J Med Genet 1983; 20: 307-309. doi:10.1136/jmg.20.4.307 [Abstract] [PDF] [Request Permissions]

Involvement of dorsal root ganglia in Fabry's disease.
N Gadoth and U Sandbank
J Med Genet 1983; 20: 309-312. doi:10.1136/jmg.20.4.309 [Abstract] [PDF] [Request Permissions]

Does sacral agenesis predispose to spina bifida?
R Magnus, J G Rogers, and E A Haan
J Med Genet 1983; 20: 313. doi:10.1136/jmg.20.4.313 [PDF] [Request Permissions]

Absence of the fragile X in a group of patients with idiopathic mental retardation.
A G Hunter, J MacDonald, and J A Evans
J Med Genet 1983; 20: 314-315. doi:10.1136/jmg.20.4.314-a [PDF] [Request Permissions]

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Genetics jobs

Show me all >>

	Editorial C A Clarke J Med Genet 1983; 20: 241-243. doi:10.1136/jmg.20.4.241 [PDF] [Request Permissions]

	Abstracts of the Joint Meeting of the Clinical Genetics Society and the Royal College of Obstetricians and Gynaecologists held at the Royal College, London, on 27 October 1982 J Med Genet 1983; 20: 300-302. doi:10.1136/jmg.20.4.300 [PDF] [Request Permissions]

	Correction J Med Genet 1983; 20: 312. doi:10.1136/jmg.20.4.312 [PDF] [Request Permissions]

	The cause(s) of neural tube defect W H James J Med Genet 1983; 20: 314. doi:10.1136/jmg.20.4.314 [PDF] [Request Permissions]

	Familial Inherited Abnormalities A W Johnston J Med Genet 1983; 20: 316. doi:10.1136/jmg.20.4.316 [PDF] [Request Permissions]

	Histocompatibility Antigens. Structure and Function Rodney Harris J Med Genet 1983; 20: 316-317. doi:10.1136/jmg.20.4.316-a [PDF] [Request Permissions]

	Genetic Variants and Strains of the Laboratory Mouse M S Deol J Med Genet 1983; 20: 317. doi:10.1136/jmg.20.4.317 [PDF] [Request Permissions]

	Animal Models of Inherited Metabolic Diseases A D Patrick J Med Genet 1983; 20: 317. doi:10.1136/jmg.20.4.317-a [PDF] [Request Permissions]

	Genetic Recombination. Understanding the Mechanisms Kay E Davies J Med Genet 1983; 20: 317-318. doi:10.1136/jmg.20.4.317-b [PDF] [Request Permissions]

	Early Diagnosis of Fetal Defects N R Dennis J Med Genet 1983; 20: 318. doi:10.1136/jmg.20.4.318 [PDF] [Request Permissions]

	The teaching of human genetics in schools. J S Fitzsimmons J Med Genet 1983; 20: 244-248. doi:10.1136/jmg.20.4.244 [PDF] [Request Permissions]

	Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences. T O'Brien, P S Harper, K E Davies, J M Murray, M Sarfarazi, and R Williamson J Med Genet 1983; 20: 249-251. doi:10.1136/jmg.20.4.249 [Abstract] [PDF] [Request Permissions]

	The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy. P S Harper, T O'Brien, J M Murray, K E Davies, P Pearson, and R Williamson J Med Genet 1983; 20: 252-254. doi:10.1136/jmg.20.4.252 [Abstract] [PDF] [Request Permissions]

	Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome. H M Kingston, N S Thomas, P L Pearson, M Sarfarazi, and P S Harper J Med Genet 1983; 20: 255-258. doi:10.1136/jmg.20.4.255 [Abstract] [PDF] [Request Permissions]

	Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe. K E Davies, J Jackson, R Williamson, P S Harper, S Ball, M Sarfarazi, L Meredith, and G Fey J Med Genet 1983; 20: 259-263. doi:10.1136/jmg.20.4.259 [Abstract] [PDF] [Request Permissions]

	The X linked recessive form of XY gonadal dysgenesis with a high incidence of gonadal germ cell tumours: clinical and genetic studies. J R Mann, J J Corkery, H J Fisher, A H Cameron, A Mayerová, U Wolf, A A Kennaugh, and V Woolley J Med Genet 1983; 20: 264-270. doi:10.1136/jmg.20.4.264 [Abstract] [PDF] [Request Permissions]

	Evaluation of segregation ratio in Wilson's disease. T Saito J Med Genet 1983; 20: 271-275. doi:10.1136/jmg.20.4.271 [Abstract] [PDF] [Request Permissions]

	Thoracic-pelvic dysostosis: a 'new' autosomal dominant form. A Bankier and D M Danks J Med Genet 1983; 20: 276-279. doi:10.1136/jmg.20.4.276 [Abstract] [PDF] [Request Permissions]

	The fragile X: a scanning electron microscope study. C J Harrison, E M Jack, T D Allen, and R Harris J Med Genet 1983; 20: 280-285. doi:10.1136/jmg.20.4.280 [Abstract] [PDF] [Request Permissions]

	Fragile X trait in a large kindred: transmission also through normal males. B C Van Roy, M C De Smedt, R A Raes, J E Dumon, and J G Leroy J Med Genet 1983; 20: 286-289. doi:10.1136/jmg.20.4.286 [Abstract] [PDF] [Request Permissions]

	Chiasma distribution, genetic lengths, and recombination fractions: a comparison between chromosomes 15 and 16. N Saadallah and M Hultén J Med Genet 1983; 20: 290-299. doi:10.1136/jmg.20.4.290 [Abstract] [PDF] [Request Permissions]

	Cardiac rhabdomyomata as a marker for the antenatal detection of tuberous sclerosis. D C Crawford, C Garrett, M Tynan, B G Neville, and L D Allan J Med Genet 1983; 20: 303-304. doi:10.1136/jmg.20.4.303 [Abstract] [PDF] [Request Permissions]

	Unusual ocular findings in an infant with cri-du-chat syndrome. S Kitsiou-Tzeli, H D Dellagrammaticas, C B Papas, I D Ladas, and C S Bartsocas J Med Genet 1983; 20: 304-307. doi:10.1136/jmg.20.4.304 [Abstract] [PDF] [Request Permissions]

	Phenazopyridine induced methaemoglobinaemia associated with decreased activity of erythrocyte cytochrome b5 reductase. J S Daly, D E Hultquist, and D L Rucknagel J Med Genet 1983; 20: 307-309. doi:10.1136/jmg.20.4.307 [Abstract] [PDF] [Request Permissions]

	Involvement of dorsal root ganglia in Fabry's disease. N Gadoth and U Sandbank J Med Genet 1983; 20: 309-312. doi:10.1136/jmg.20.4.309 [Abstract] [PDF] [Request Permissions]

	Does sacral agenesis predispose to spina bifida? R Magnus, J G Rogers, and E A Haan J Med Genet 1983; 20: 313. doi:10.1136/jmg.20.4.313 [PDF] [Request Permissions]

	Absence of the fragile X in a group of patients with idiopathic mental retardation. A G Hunter, J MacDonald, and J A Evans J Med Genet 1983; 20: 314-315. doi:10.1136/jmg.20.4.314-a [PDF] [Request Permissions]