J Med Genet -- Table of Contents (22 [4])

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August 1985 (Volume 22, Number 4). [Index by author]

		Correspondence Book Reviews Research Article

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Correspondence

Triple aneuploidy
Digamber S Borgaonkar
J Med Genet 1985; 22: 319. doi:10.1136/jmg.22.4.319 [PDF] [Request Permissions]

Correspondence
F M Pope and A C Nicholls
J Med Genet 1985; 22: 320. doi:10.1136/jmg.22.4.320 [PDF] [Request Permissions]

Book Reviews

Practical Genetic Counselling
Rodney Harris
J Med Genet 1985; 22: 324. doi:10.1136/jmg.22.4.324 [PDF] [Request Permissions]

Genetic Analysis of the Cell Surface
Alan Emery
J Med Genet 1985; 22: 324-325. doi:10.1136/jmg.22.4.324-a [PDF] [Request Permissions]

Genetic Aspects of Speech and Language Disorders
M Baraitser
J Med Genet 1985; 22: 325. doi:10.1136/jmg.22.4.325 [PDF] [Request Permissions]

The Hereditary Ataxias and Related Disorders
Sarah Bundey
J Med Genet 1985; 22: 325-326. doi:10.1136/jmg.22.4.325-a [PDF] [Request Permissions]

Annual Review of Genetics
Peter S Harper
J Med Genet 1985; 22: 326. doi:10.1136/jmg.22.4.326 [PDF] [Request Permissions]

Mutagenicity, Carcinogenicity, and Teratogenicity of Industrial Pollutants
J Parry
J Med Genet 1985; 22: 326-327. doi:10.1136/jmg.22.4.326-a [PDF] [Request Permissions]

Research Article

Gene mapping and medical genetics.
P S Harper
J Med Genet 1985; 22: 241-242. doi:10.1136/jmg.22.4.241 [PDF] [Request Permissions]

Molecular genetics of the human X chromosome.
K E Davies
J Med Genet 1985; 22: 243-249. doi:10.1136/jmg.22.4.243 [Abstract] [PDF] [Request Permissions]

A population study of adult onset limb-girdle muscular dystrophy.
J R Yates and A E Emery
J Med Genet 1985; 22: 250-257. doi:10.1136/jmg.22.4.250 [Abstract] [PDF] [Request Permissions]

A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology.
S Bundey, T P Webb, A Thake, and J Todd
J Med Genet 1985; 22: 258-266. doi:10.1136/jmg.22.4.258 [Abstract] [PDF] [Request Permissions]

Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder.
R A Pagon, T D Bird, J C Detter, and I Pierce
J Med Genet 1985; 22: 267-273. doi:10.1136/jmg.22.4.267 [Abstract] [PDF] [Request Permissions]

The inheritance of primary lymphoedema.
R F Dale
J Med Genet 1985; 22: 274-278. doi:10.1136/jmg.22.4.274 [Abstract] [PDF] [Request Permissions]

Zygosity determination in newborn twins using DNA variants.
C Derom, E Bakker, R Vlietinck, R Derom, H Van den Berghe, M Thiery, and P Pearson
J Med Genet 1985; 22: 279-282. doi:10.1136/jmg.22.4.279 [Abstract] [PDF] [Request Permissions]

A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.
J L Watt, I A Olson, A W Johnston, H S Ross, D A Couzin, and G S Stephen
J Med Genet 1985; 22: 283-287. doi:10.1136/jmg.22.4.283 [Abstract] [PDF] [Request Permissions]

Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
M Aksoy, A Kutlar, F Kutlar, G Dinçol, S Erdem, and S Bastesbihçi
J Med Genet 1985; 22: 288-290. doi:10.1136/jmg.22.4.288 [Abstract] [PDF] [Request Permissions]

Admission of Hb S heterozygotes to a general hospital is relatively reduced in malarial areas.
B Colombo and L Felicetti
J Med Genet 1985; 22: 291-292. doi:10.1136/jmg.22.4.291 [Abstract] [PDF] [Request Permissions]

Evaluation of haematological findings in 50 Bahraini patients with sickle cell disease and in some of their parents.
M A Buhazza, A B Bikhazi, and F P Khouri
J Med Genet 1985; 22: 293-295. doi:10.1136/jmg.22.4.293 [Abstract] [PDF] [Request Permissions]

Cornelia de Lange syndrome in several members of the same family.
D Kumar, C E Blank, and B L Griffiths
J Med Genet 1985; 22: 296-300. doi:10.1136/jmg.22.4.296 [Abstract] [PDF] [Request Permissions]

High incidence of Meckel's syndrome in Gujarati Indians.
I D Young, A B Rickett, and M Clarke
J Med Genet 1985; 22: 301-304. doi:10.1136/jmg.22.4.301 [Abstract] [PDF] [Request Permissions]

Gene deletion in an Italian haemophilia B subject.
F Bernardi, L del Senno, R Barbieri, D Buzzoni, R Gambari, G Marchetti, F Conconi, F Panicucci, M Positano, and S Pitruzzello
J Med Genet 1985; 22: 305-307. doi:10.1136/jmg.22.4.305 [Abstract] [PDF] [Request Permissions]

Two brothers with Martsolf's syndrome.
J M Sánchez, C Barreiro, and H Freilij
J Med Genet 1985; 22: 308-310. doi:10.1136/jmg.22.4.308 [Abstract] [PDF] [Request Permissions]

Familial pulmonary valve stenosis, atrial septal defect, and unique electrocardiogram abnormalities.
A A Ciuffo, E Cunningham, and T A Traill
J Med Genet 1985; 22: 311-313. doi:10.1136/jmg.22.4.311 [Abstract] [PDF] [Request Permissions]

Complex translocation in a boy with trichorhinophalangeal syndrome.
L M Sánchez, J D Labarta, T C De Negrotti, and A M Migliorini
J Med Genet 1985; 22: 314-316. doi:10.1136/jmg.22.4.314 [Abstract] [PDF] [Request Permissions]

Interstitial deletion of chromosome 7p detected antenatally.
K Marks, L Hill, R G Chitham, and W L Whitehouse
J Med Genet 1985; 22: 316-318. doi:10.1136/jmg.22.4.316 [Abstract] [PDF] [Request Permissions]

A possible mechanism underlying the sex selectivity of neural tube defect.
W H James
J Med Genet 1985; 22: 319. doi:10.1136/jmg.22.4.319-a [PDF] [Request Permissions]

Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta.
J P Gage
J Med Genet 1985; 22: 319-320. doi:10.1136/jmg.22.4.319-b [PDF] [Request Permissions]

HLA antigens in South African Afrikaners with heterozygous familial hypercholesterolaemia.
S G Baker, A Rabson, R Shires, B I Joffe, and H C Seftel
J Med Genet 1985; 22: 320-321. doi:10.1136/jmg.22.4.320-a [PDF] [Request Permissions]

Prenatal screening for Down syndrome.
M J Seller
J Med Genet 1985; 22: 321-323. doi:10.1136/jmg.22.4.321 [PDF] [Request Permissions]

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	Triple aneuploidy Digamber S Borgaonkar J Med Genet 1985; 22: 319. doi:10.1136/jmg.22.4.319 [PDF] [Request Permissions]

	Correspondence F M Pope and A C Nicholls J Med Genet 1985; 22: 320. doi:10.1136/jmg.22.4.320 [PDF] [Request Permissions]

	Practical Genetic Counselling Rodney Harris J Med Genet 1985; 22: 324. doi:10.1136/jmg.22.4.324 [PDF] [Request Permissions]

	Genetic Analysis of the Cell Surface Alan Emery J Med Genet 1985; 22: 324-325. doi:10.1136/jmg.22.4.324-a [PDF] [Request Permissions]

	Genetic Aspects of Speech and Language Disorders M Baraitser J Med Genet 1985; 22: 325. doi:10.1136/jmg.22.4.325 [PDF] [Request Permissions]

	The Hereditary Ataxias and Related Disorders Sarah Bundey J Med Genet 1985; 22: 325-326. doi:10.1136/jmg.22.4.325-a [PDF] [Request Permissions]

	Annual Review of Genetics Peter S Harper J Med Genet 1985; 22: 326. doi:10.1136/jmg.22.4.326 [PDF] [Request Permissions]

	Mutagenicity, Carcinogenicity, and Teratogenicity of Industrial Pollutants J Parry J Med Genet 1985; 22: 326-327. doi:10.1136/jmg.22.4.326-a [PDF] [Request Permissions]

	Gene mapping and medical genetics. P S Harper J Med Genet 1985; 22: 241-242. doi:10.1136/jmg.22.4.241 [PDF] [Request Permissions]

	Molecular genetics of the human X chromosome. K E Davies J Med Genet 1985; 22: 243-249. doi:10.1136/jmg.22.4.243 [Abstract] [PDF] [Request Permissions]

	A population study of adult onset limb-girdle muscular dystrophy. J R Yates and A E Emery J Med Genet 1985; 22: 250-257. doi:10.1136/jmg.22.4.250 [Abstract] [PDF] [Request Permissions]

	A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology. S Bundey, T P Webb, A Thake, and J Todd J Med Genet 1985; 22: 258-266. doi:10.1136/jmg.22.4.258 [Abstract] [PDF] [Request Permissions]

	Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder. R A Pagon, T D Bird, J C Detter, and I Pierce J Med Genet 1985; 22: 267-273. doi:10.1136/jmg.22.4.267 [Abstract] [PDF] [Request Permissions]

	The inheritance of primary lymphoedema. R F Dale J Med Genet 1985; 22: 274-278. doi:10.1136/jmg.22.4.274 [Abstract] [PDF] [Request Permissions]

	Zygosity determination in newborn twins using DNA variants. C Derom, E Bakker, R Vlietinck, R Derom, H Van den Berghe, M Thiery, and P Pearson J Med Genet 1985; 22: 279-282. doi:10.1136/jmg.22.4.279 [Abstract] [PDF] [Request Permissions]

	A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome. J L Watt, I A Olson, A W Johnston, H S Ross, D A Couzin, and G S Stephen J Med Genet 1985; 22: 283-287. doi:10.1136/jmg.22.4.283 [Abstract] [PDF] [Request Permissions]

	Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace. M Aksoy, A Kutlar, F Kutlar, G Dinçol, S Erdem, and S Bastesbihçi J Med Genet 1985; 22: 288-290. doi:10.1136/jmg.22.4.288 [Abstract] [PDF] [Request Permissions]

	Admission of Hb S heterozygotes to a general hospital is relatively reduced in malarial areas. B Colombo and L Felicetti J Med Genet 1985; 22: 291-292. doi:10.1136/jmg.22.4.291 [Abstract] [PDF] [Request Permissions]

	Evaluation of haematological findings in 50 Bahraini patients with sickle cell disease and in some of their parents. M A Buhazza, A B Bikhazi, and F P Khouri J Med Genet 1985; 22: 293-295. doi:10.1136/jmg.22.4.293 [Abstract] [PDF] [Request Permissions]

	Cornelia de Lange syndrome in several members of the same family. D Kumar, C E Blank, and B L Griffiths J Med Genet 1985; 22: 296-300. doi:10.1136/jmg.22.4.296 [Abstract] [PDF] [Request Permissions]

	High incidence of Meckel's syndrome in Gujarati Indians. I D Young, A B Rickett, and M Clarke J Med Genet 1985; 22: 301-304. doi:10.1136/jmg.22.4.301 [Abstract] [PDF] [Request Permissions]

	Gene deletion in an Italian haemophilia B subject. F Bernardi, L del Senno, R Barbieri, D Buzzoni, R Gambari, G Marchetti, F Conconi, F Panicucci, M Positano, and S Pitruzzello J Med Genet 1985; 22: 305-307. doi:10.1136/jmg.22.4.305 [Abstract] [PDF] [Request Permissions]

	Two brothers with Martsolf's syndrome. J M Sánchez, C Barreiro, and H Freilij J Med Genet 1985; 22: 308-310. doi:10.1136/jmg.22.4.308 [Abstract] [PDF] [Request Permissions]

	Familial pulmonary valve stenosis, atrial septal defect, and unique electrocardiogram abnormalities. A A Ciuffo, E Cunningham, and T A Traill J Med Genet 1985; 22: 311-313. doi:10.1136/jmg.22.4.311 [Abstract] [PDF] [Request Permissions]

	Complex translocation in a boy with trichorhinophalangeal syndrome. L M Sánchez, J D Labarta, T C De Negrotti, and A M Migliorini J Med Genet 1985; 22: 314-316. doi:10.1136/jmg.22.4.314 [Abstract] [PDF] [Request Permissions]

	Interstitial deletion of chromosome 7p detected antenatally. K Marks, L Hill, R G Chitham, and W L Whitehouse J Med Genet 1985; 22: 316-318. doi:10.1136/jmg.22.4.316 [Abstract] [PDF] [Request Permissions]

	A possible mechanism underlying the sex selectivity of neural tube defect. W H James J Med Genet 1985; 22: 319. doi:10.1136/jmg.22.4.319-a [PDF] [Request Permissions]

	Clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. J P Gage J Med Genet 1985; 22: 319-320. doi:10.1136/jmg.22.4.319-b [PDF] [Request Permissions]

	HLA antigens in South African Afrikaners with heterozygous familial hypercholesterolaemia. S G Baker, A Rabson, R Shires, B I Joffe, and H C Seftel J Med Genet 1985; 22: 320-321. doi:10.1136/jmg.22.4.320-a [PDF] [Request Permissions]

	Prenatal screening for Down syndrome. M J Seller J Med Genet 1985; 22: 321-323. doi:10.1136/jmg.22.4.321 [PDF] [Request Permissions]