J Med Genet -- Table of Contents (13 [1])

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February 1976 (Volume 13, Number 1). [Index by author]

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Articles

Blood groups and other polymorphisms in multiple sclerosis
J. L. MacDonald, D. F. Roberts, D. A. Shaw, and M. Saunders
J Med Genet 1976; 13: 30-33. doi:10.1136/jmg.13.1.30 [Abstract] [PDF] [Request Permissions]

Research Article

Aspects of pre-eclamptic toxaemia of pregnancy, consanguinity, twinning in Ankara.
A C Stevenson, B Say, S Ustaoglu, and Z Durmus
J Med Genet 1976; 13: 1-8. doi:10.1136/jmg.13.1.1 [Abstract] [PDF] [Request Permissions]

Congenital malformations of the central nervous system in spontaneous abortions.
M R Creasy and E D Alberman
J Med Genet 1976; 13: 9-16. doi:10.1136/jmg.13.1.9 [Abstract] [PDF] [Request Permissions]

Polymorphic acetylation of nitrazepam.
A K Karim and D A Evans
J Med Genet 1976; 13: 17-19. doi:10.1136/jmg.13.1.17 [Abstract] [PDF] [Request Permissions]

Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia.
D J Weatherall, J B Clegg, P F Milner, G W Marsh, F G Bolton, and G R Serjeant
J Med Genet 1976; 13: 20-26. doi:10.1136/jmg.13.1.20 [Abstract] [PDF] [Request Permissions]

Consanguinity and familial mental retardation.
B S Sridhara Rama Rao and H S Narayanan
J Med Genet 1976; 13: 27-29. doi:10.1136/jmg.13.1.27 [Abstract] [PDF] [Request Permissions]

Behaviour of cell cultures from human amniotic fluid.
L Hasholt
J Med Genet 1976; 13: 34-37. doi:10.1136/jmg.13.1.34 [Abstract] [PDF] [Request Permissions]

New allele at cholinesterase locus 1.
P J Garry, A A Dietz, T Lubrano, P C Ford, K James, and H M Rubinstein
J Med Genet 1976; 13: 38-42. doi:10.1136/jmg.13.1.38 [Abstract] [PDF] [Request Permissions]

E1j, a quantitative variant at cholinesterase locus 1: immunological evidence.
H M Rubinstein, A A Dietz, T Lubrano, and P J Garry
J Med Genet 1976; 13: 43-45. doi:10.1136/jmg.13.1.43 [Abstract] [PDF] [Request Permissions]

'Durate variant with clinical signs' has alpha1 -antitrypsin genotype ZZ.
L R Weitkamp, J W Sayre, R H Schwartz, R Doherty, and S A Khera
J Med Genet 1976; 13: 46-48. doi:10.1136/jmg.13.1.46 [Abstract] [PDF] [Request Permissions]

Prenatal diagnosis of Wolman's disease.
A D Patrick, P Willcox, R Stephens, and V G Kenyon
J Med Genet 1976; 13: 49-51. doi:10.1136/jmg.13.1.49 [Abstract] [PDF] [Request Permissions]

The Gardner syndrome: increased tetraploidy in cultured skin fibroblast.
B S Danes
J Med Genet 1976; 13: 52-56. doi:10.1136/jmg.13.1.52 [Abstract] [PDF] [Request Permissions]

Familial 'partial 9p' trisomy: six cases and four carriers in three generations.
W R Centerwall, K S Miller, and L M Reeves
J Med Genet 1976; 13: 57-61. doi:10.1136/jmg.13.1.57 [Abstract] [PDF] [Request Permissions]

A note on the inheritance of the hereditary persistence of fetal haemoglobin and the delta-chain variant Hb-A2'.
T H Huisman, M E Gravely, and R Sox
J Med Genet 1976; 13: 62-63. doi:10.1136/jmg.13.1.62 [PDF] [Request Permissions]

Monozygotic twins discordant for sex.
R Schmidt, E H Sobel, H M Nitowsky, H Dar, and F H Allen, Jr
J Med Genet 1976; 13: 64-68. doi:10.1136/jmg.13.1.64 [Abstract] [PDF] [Request Permissions]

An XX female with sexual infantilism, absent gonads, and lack of Müllerian ducts.
G Levinson, A Zárate, R Guzmán-Toledano, E S Canales, and M Jiménez
J Med Genet 1976; 13: 68-69. doi:10.1136/jmg.13.1.68 [Abstract] [PDF] [Request Permissions]

Further observations on the Birmingham chimaera.
G W Bird, D A Battey, P Greenwell, C W Mortimer, W M Watkins, and J Wingham
J Med Genet 1976; 13: 70-71. doi:10.1136/jmg.13.1.70 [Abstract] [PDF] [Request Permissions]

A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+).
V Ventruto, A Cali, L Farina, B Festa, I Ricciardi, and L Sebastio
J Med Genet 1976; 13: 71-75. doi:10.1136/jmg.13.1.71 [Abstract] [PDF] [Request Permissions]

A probable case of mutation in Huntington's disease.
E Chiu and C J Brackenridge
J Med Genet 1976; 13: 75-77. doi:10.1136/jmg.13.1.75 [Abstract] [PDF] [Request Permissions]

Trigonocephaly and associated minor anomalies in mother and son.
A G Hunter, N L Rudd, and H J Hoffmann
J Med Genet 1976; 13: 77-79. doi:10.1136/jmg.13.1.77 [Abstract] [PDF] [Request Permissions]

Letter: Cerebral gigantism.
P L Townes
J Med Genet 1976; 13: 80. doi:10.1136/jmg.13.1.80 [PDF] [Request Permissions]

Letter: Diagnositc problems in cerebral gigantism.
M M Cohen
J Med Genet 1976; 13: 80. doi:10.1136/jmg.13.1.80-a [PDF] [Request Permissions]

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	Blood groups and other polymorphisms in multiple sclerosis J. L. MacDonald, D. F. Roberts, D. A. Shaw, and M. Saunders J Med Genet 1976; 13: 30-33. doi:10.1136/jmg.13.1.30 [Abstract] [PDF] [Request Permissions]

	Aspects of pre-eclamptic toxaemia of pregnancy, consanguinity, twinning in Ankara. A C Stevenson, B Say, S Ustaoglu, and Z Durmus J Med Genet 1976; 13: 1-8. doi:10.1136/jmg.13.1.1 [Abstract] [PDF] [Request Permissions]

	Congenital malformations of the central nervous system in spontaneous abortions. M R Creasy and E D Alberman J Med Genet 1976; 13: 9-16. doi:10.1136/jmg.13.1.9 [Abstract] [PDF] [Request Permissions]

	Polymorphic acetylation of nitrazepam. A K Karim and D A Evans J Med Genet 1976; 13: 17-19. doi:10.1136/jmg.13.1.17 [Abstract] [PDF] [Request Permissions]

	Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia. D J Weatherall, J B Clegg, P F Milner, G W Marsh, F G Bolton, and G R Serjeant J Med Genet 1976; 13: 20-26. doi:10.1136/jmg.13.1.20 [Abstract] [PDF] [Request Permissions]

	Consanguinity and familial mental retardation. B S Sridhara Rama Rao and H S Narayanan J Med Genet 1976; 13: 27-29. doi:10.1136/jmg.13.1.27 [Abstract] [PDF] [Request Permissions]

	Behaviour of cell cultures from human amniotic fluid. L Hasholt J Med Genet 1976; 13: 34-37. doi:10.1136/jmg.13.1.34 [Abstract] [PDF] [Request Permissions]

	New allele at cholinesterase locus 1. P J Garry, A A Dietz, T Lubrano, P C Ford, K James, and H M Rubinstein J Med Genet 1976; 13: 38-42. doi:10.1136/jmg.13.1.38 [Abstract] [PDF] [Request Permissions]

	E1j, a quantitative variant at cholinesterase locus 1: immunological evidence. H M Rubinstein, A A Dietz, T Lubrano, and P J Garry J Med Genet 1976; 13: 43-45. doi:10.1136/jmg.13.1.43 [Abstract] [PDF] [Request Permissions]

	'Durate variant with clinical signs' has alpha1 -antitrypsin genotype ZZ. L R Weitkamp, J W Sayre, R H Schwartz, R Doherty, and S A Khera J Med Genet 1976; 13: 46-48. doi:10.1136/jmg.13.1.46 [Abstract] [PDF] [Request Permissions]

	Prenatal diagnosis of Wolman's disease. A D Patrick, P Willcox, R Stephens, and V G Kenyon J Med Genet 1976; 13: 49-51. doi:10.1136/jmg.13.1.49 [Abstract] [PDF] [Request Permissions]

	The Gardner syndrome: increased tetraploidy in cultured skin fibroblast. B S Danes J Med Genet 1976; 13: 52-56. doi:10.1136/jmg.13.1.52 [Abstract] [PDF] [Request Permissions]

	Familial 'partial 9p' trisomy: six cases and four carriers in three generations. W R Centerwall, K S Miller, and L M Reeves J Med Genet 1976; 13: 57-61. doi:10.1136/jmg.13.1.57 [Abstract] [PDF] [Request Permissions]

	A note on the inheritance of the hereditary persistence of fetal haemoglobin and the delta-chain variant Hb-A2'. T H Huisman, M E Gravely, and R Sox J Med Genet 1976; 13: 62-63. doi:10.1136/jmg.13.1.62 [PDF] [Request Permissions]

	Monozygotic twins discordant for sex. R Schmidt, E H Sobel, H M Nitowsky, H Dar, and F H Allen, Jr J Med Genet 1976; 13: 64-68. doi:10.1136/jmg.13.1.64 [Abstract] [PDF] [Request Permissions]

	An XX female with sexual infantilism, absent gonads, and lack of Müllerian ducts. G Levinson, A Zárate, R Guzmán-Toledano, E S Canales, and M Jiménez J Med Genet 1976; 13: 68-69. doi:10.1136/jmg.13.1.68 [Abstract] [PDF] [Request Permissions]

	Further observations on the Birmingham chimaera. G W Bird, D A Battey, P Greenwell, C W Mortimer, W M Watkins, and J Wingham J Med Genet 1976; 13: 70-71. doi:10.1136/jmg.13.1.70 [Abstract] [PDF] [Request Permissions]

	A case of hypogonadotrophic hypogonadism with anosmia (Kallmann's syndrome) in a male, with familial incidence of a small metacentric chromosome (47,XX, mat?+). V Ventruto, A Cali, L Farina, B Festa, I Ricciardi, and L Sebastio J Med Genet 1976; 13: 71-75. doi:10.1136/jmg.13.1.71 [Abstract] [PDF] [Request Permissions]

	A probable case of mutation in Huntington's disease. E Chiu and C J Brackenridge J Med Genet 1976; 13: 75-77. doi:10.1136/jmg.13.1.75 [Abstract] [PDF] [Request Permissions]

	Trigonocephaly and associated minor anomalies in mother and son. A G Hunter, N L Rudd, and H J Hoffmann J Med Genet 1976; 13: 77-79. doi:10.1136/jmg.13.1.77 [Abstract] [PDF] [Request Permissions]

	Letter: Cerebral gigantism. P L Townes J Med Genet 1976; 13: 80. doi:10.1136/jmg.13.1.80 [PDF] [Request Permissions]

	Letter: Diagnositc problems in cerebral gigantism. M M Cohen J Med Genet 1976; 13: 80. doi:10.1136/jmg.13.1.80-a [PDF] [Request Permissions]