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September 1975 (Volume 12, Number 3). [Index by author]

		Book Reviews Research Article

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Book Reviews

The Biology of Racial Integration
D. F. Roberts
J Med Genet 1975; 12: 315. doi:10.1136/jmg.12.3.315 [PDF] [Request Permissions]

Practical Human Cytogenetics
Stanley Walker
J Med Genet 1975; 12: 315-316. doi:10.1136/jmg.12.3.315-a [PDF] [Request Permissions]

Handbuch der Inneren Medizin, vol 7—Erbliche Defekte des Kohlenhydrat-Aminosauren-und Proteinstoff-wechsels
D. N. Raine
J Med Genet 1975; 12: 316. doi:10.1136/jmg.12.3.316 [PDF] [Request Permissions]

X-Linked Mental Retardation and Verbal Disability
Renata Lax
J Med Genet 1975; 12: 316. doi:10.1136/jmg.12.3.316-a [PDF] [Request Permissions]

Research Article

Attitudes of patients and their relatives to Huntington's disease.
R Stern and R Eldridge
J Med Genet 1975; 12: 217-223. doi:10.1136/jmg.12.3.217 [Abstract] [PDF] [Request Permissions]

Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells.
E Young, P Willcox, A E Whitfield, and A D Patrick
J Med Genet 1975; 12: 224-229. doi:10.1136/jmg.12.3.224 [Abstract] [PDF] [Request Permissions]

Transplacental passage of blood cells.
J Schröder
J Med Genet 1975; 12: 230-242. doi:10.1136/jmg.12.3.230 [PDF] [Request Permissions]

Development of dermal ridges in the fetus.
M Okajima
J Med Genet 1975; 12: 243-250. doi:10.1136/jmg.12.3.243 [Abstract] [PDF] [Request Permissions]

Specific chromosome aberrations in ataxia telangiectasia.
J M Oxford, D G Harnden, J M Parrington, and J D Delhanty
J Med Genet 1975; 12: 251-262. doi:10.1136/jmg.12.3.251 [Abstract] [PDF] [Request Permissions]

Alpha1-antitrypsin phenotypes in sex chromosome mosaicism.
F Kueppers, P O'Brien, E Passarge, and H W Rüdiger
J Med Genet 1975; 12: 263-264. doi:10.1136/jmg.12.3.263 [Abstract] [PDF] [Request Permissions]

Identification of C trisomies in human abortuses.
J Boué, A Boué, C Deluchat, N Perraudin, and F Yvert
J Med Genet 1975; 12: 265-268. doi:10.1136/jmg.12.3.265 [Abstract] [PDF] [Request Permissions]

Homozygous haemoglobin D Punjab.
C Politis-Tsegos, P Kynoch, A Lang, H Lehmann, P A Lorkin, R Stathopoulou, and G Wakefield
J Med Genet 1975; 12: 269-274. doi:10.1136/jmg.12.3.269 [Abstract] [PDF] [Request Permissions]

Haemoglobin Lepore in Cyprus.
Z Zachariadis, P E Nute, and G Stamatoyannopoulos
J Med Genet 1975; 12: 275-279. doi:10.1136/jmg.12.3.275 [Abstract] [PDF] [Request Permissions]

Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica.
R Wynne-Davies
J Med Genet 1975; 12: 280-288. doi:10.1136/jmg.12.3.280 [Abstract] [PDF] [Request Permissions]

Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs.
C K Ho, R L Kaufman, and S M Podos
J Med Genet 1975; 12: 289-293. doi:10.1136/jmg.12.3.289 [Abstract] [PDF] [Request Permissions]

Haemoglobin Hasharon in a north Italian community.
R Alberti, G M Mariuzzi, M Marinucci, E Bruni, and L Tenteri
J Med Genet 1975; 12: 294-296. doi:10.1136/jmg.12.3.294 [Abstract] [PDF] [Request Permissions]

A new case of haemoglobin Bucuresti in a Cuban family: further functional studies.
B Colombe, M P Benitez, L Bernini, J Elien, H Wajeman, and D Labie
J Med Genet 1975; 12: 297-298. doi:10.1136/jmg.12.3.297 [Abstract] [PDF] [Request Permissions]

Klinefelter's syndrome associated with a D/D translocation.
M Sparagana and G P Smith
J Med Genet 1975; 12: 299-301. doi:10.1136/jmg.12.3.299 [Abstract] [PDF] [Request Permissions]

Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).
V B Penehaszadeh and R Coco
J Med Genet 1975; 12: 301-305. doi:10.1136/jmg.12.3.301 [Abstract] [PDF] [Request Permissions]

Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.
L M Stern and A R Mureh
J Med Genet 1975; 12: 305-307. doi:10.1136/jmg.12.3.305 [Abstract] [PDF] [Request Permissions]

A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs.
N Freire-Maia, V A Fortes, L C Pereira, J M Opitz, F A Marcalle, and I J Cavalli
J Med Genet 1975; 12: 308-310. doi:10.1136/jmg.12.3.308 [Abstract] [PDF] [Request Permissions]

A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).
M K Mason, D A Spencer, and A Rutter
J Med Genet 1975; 12: 310-314. doi:10.1136/jmg.12.3.310 [Abstract] [PDF] [Request Permissions]

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	The Biology of Racial Integration D. F. Roberts J Med Genet 1975; 12: 315. doi:10.1136/jmg.12.3.315 [PDF] [Request Permissions]

	Practical Human Cytogenetics Stanley Walker J Med Genet 1975; 12: 315-316. doi:10.1136/jmg.12.3.315-a [PDF] [Request Permissions]

	Handbuch der Inneren Medizin, vol 7—Erbliche Defekte des Kohlenhydrat-Aminosauren-und Proteinstoff-wechsels D. N. Raine J Med Genet 1975; 12: 316. doi:10.1136/jmg.12.3.316 [PDF] [Request Permissions]

	X-Linked Mental Retardation and Verbal Disability Renata Lax J Med Genet 1975; 12: 316. doi:10.1136/jmg.12.3.316-a [PDF] [Request Permissions]

	Attitudes of patients and their relatives to Huntington's disease. R Stern and R Eldridge J Med Genet 1975; 12: 217-223. doi:10.1136/jmg.12.3.217 [Abstract] [PDF] [Request Permissions]

	Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells. E Young, P Willcox, A E Whitfield, and A D Patrick J Med Genet 1975; 12: 224-229. doi:10.1136/jmg.12.3.224 [Abstract] [PDF] [Request Permissions]

	Transplacental passage of blood cells. J Schröder J Med Genet 1975; 12: 230-242. doi:10.1136/jmg.12.3.230 [PDF] [Request Permissions]

	Development of dermal ridges in the fetus. M Okajima J Med Genet 1975; 12: 243-250. doi:10.1136/jmg.12.3.243 [Abstract] [PDF] [Request Permissions]

	Specific chromosome aberrations in ataxia telangiectasia. J M Oxford, D G Harnden, J M Parrington, and J D Delhanty J Med Genet 1975; 12: 251-262. doi:10.1136/jmg.12.3.251 [Abstract] [PDF] [Request Permissions]

	Alpha1-antitrypsin phenotypes in sex chromosome mosaicism. F Kueppers, P O'Brien, E Passarge, and H W Rüdiger J Med Genet 1975; 12: 263-264. doi:10.1136/jmg.12.3.263 [Abstract] [PDF] [Request Permissions]

	Identification of C trisomies in human abortuses. J Boué, A Boué, C Deluchat, N Perraudin, and F Yvert J Med Genet 1975; 12: 265-268. doi:10.1136/jmg.12.3.265 [Abstract] [PDF] [Request Permissions]

	Homozygous haemoglobin D Punjab. C Politis-Tsegos, P Kynoch, A Lang, H Lehmann, P A Lorkin, R Stathopoulou, and G Wakefield J Med Genet 1975; 12: 269-274. doi:10.1136/jmg.12.3.269 [Abstract] [PDF] [Request Permissions]

	Haemoglobin Lepore in Cyprus. Z Zachariadis, P E Nute, and G Stamatoyannopoulos J Med Genet 1975; 12: 275-279. doi:10.1136/jmg.12.3.275 [Abstract] [PDF] [Request Permissions]

	Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica. R Wynne-Davies J Med Genet 1975; 12: 280-288. doi:10.1136/jmg.12.3.280 [Abstract] [PDF] [Request Permissions]

	Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs. C K Ho, R L Kaufman, and S M Podos J Med Genet 1975; 12: 289-293. doi:10.1136/jmg.12.3.289 [Abstract] [PDF] [Request Permissions]

	Haemoglobin Hasharon in a north Italian community. R Alberti, G M Mariuzzi, M Marinucci, E Bruni, and L Tenteri J Med Genet 1975; 12: 294-296. doi:10.1136/jmg.12.3.294 [Abstract] [PDF] [Request Permissions]

	A new case of haemoglobin Bucuresti in a Cuban family: further functional studies. B Colombe, M P Benitez, L Bernini, J Elien, H Wajeman, and D Labie J Med Genet 1975; 12: 297-298. doi:10.1136/jmg.12.3.297 [Abstract] [PDF] [Request Permissions]

	Klinefelter's syndrome associated with a D/D translocation. M Sparagana and G P Smith J Med Genet 1975; 12: 299-301. doi:10.1136/jmg.12.3.299 [Abstract] [PDF] [Request Permissions]

	Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-). V B Penehaszadeh and R Coco J Med Genet 1975; 12: 301-305. doi:10.1136/jmg.12.3.301 [Abstract] [PDF] [Request Permissions]

	Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. L M Stern and A R Mureh J Med Genet 1975; 12: 305-307. doi:10.1136/jmg.12.3.305 [Abstract] [PDF] [Request Permissions]

	A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs. N Freire-Maia, V A Fortes, L C Pereira, J M Opitz, F A Marcalle, and I J Cavalli J Med Genet 1975; 12: 308-310. doi:10.1136/jmg.12.3.308 [Abstract] [PDF] [Request Permissions]

	A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-). M K Mason, D A Spencer, and A Rutter J Med Genet 1975; 12: 310-314. doi:10.1136/jmg.12.3.310 [Abstract] [PDF] [Request Permissions]