J Med Genet -- Table of Contents (17 [1])

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February 1980 (Volume 17, Number 1). [Index by author]

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Articles

Inbreeding effects on fetal growth and development
P S S Rao and S G Inbaraj
J Med Genet 1980; 17: 27-33. doi:10.1136/jmg.17.1.27 [Abstract] [PDF] [Request Permissions]

Book Reviews

Elemente der klinischen Genetik. Grundlagen und Anwendung der Humangenetik in Studium und Praxis
Andrew P Read
J Med Genet 1980; 17: 77. doi:10.1136/jmg.17.1.77 [PDF] [Request Permissions]

Metabolic Disease in Childhood
J V Leonard
J Med Genet 1980; 17: 77-78. doi:10.1136/jmg.17.1.77-a [PDF] [Request Permissions]

Human Genetics (Outline Studies in Biology)
A W Johnston
J Med Genet 1980; 17: 78-79. doi:10.1136/jmg.17.1.78 [PDF] [Request Permissions]

Genetics and Cancer in Man
D F Roberts
J Med Genet 1980; 17: 79-80. doi:10.1136/jmg.17.1.79 [PDF] [Request Permissions]

Chemical Mutagens. Principles and Methods for their Detection
B A Bridges
J Med Genet 1980; 17: 80. doi:10.1136/jmg.17.1.80 [PDF] [Request Permissions]

Research Article

Haems and chlorophylls: comparison of function and formation.
G A Hendry and O T Jones
J Med Genet 1980; 17: 1-14. doi:10.1136/jmg.17.1.1 [PDF] [Request Permissions]

An overall genetic risk assessment for radiological protection purposes.
P Oftedal and A G Searle
J Med Genet 1980; 17: 15-20. doi:10.1136/jmg.17.1.15 [Abstract] [PDF] [Request Permissions]

Angiokeratoma corporis diffusum with features of a mucopolysaccharidosis.
D I McCallum, R F Macadam, and A W Johnston
J Med Genet 1980; 17: 21-26. doi:10.1136/jmg.17.1.21 [Abstract] [PDF] [Request Permissions]

Sickle cell disease in Sicily.
E F Roth, Jr, G Schiliro, A Russo, S Musumeci, E Rachmilewitz, V Neske, and R Nagel
J Med Genet 1980; 17: 34-38. doi:10.1136/jmg.17.1.34 [Abstract] [PDF] [Request Permissions]

Dominant inheritance in a family with primary atrophic rhinitis.
J R Sibert and R P Barton
J Med Genet 1980; 17: 39-40. doi:10.1136/jmg.17.1.39 [Abstract] [PDF] [Request Permissions]

Sex-influenced expression of Madelung's deformity in a family of dyschondrosteosis.
J R Lichtenstein, M Sundaram, and R Burdge
J Med Genet 1980; 17: 41-43. doi:10.1136/jmg.17.1.41 [Abstract] [PDF] [Request Permissions]

High resolution of a small pericentric inversion of chromosome 11.
H Autio-Harmainen and A De La Chapelle
J Med Genet 1980; 17: 44-47. doi:10.1136/jmg.17.1.44 [Abstract] [PDF] [Request Permissions]

Trisomy 21 mosaicism in two successive generations in a family.
J C Parke, Jr, F S Grass, R Pixley, and J Deal
J Med Genet 1980; 17: 48-49. doi:10.1136/jmg.17.1.48 [Abstract] [PDF] [Request Permissions]

Dermatoglyphic findings in Poland's syndrome.
M Atasu
J Med Genet 1980; 17: 50-52. doi:10.1136/jmg.17.1.50 [Abstract] [PDF] [Request Permissions]

Frontometaphyseal dysplasia: autosomal dominant or X-linked?
P Beighton and H Hamersma
J Med Genet 1980; 17: 53-56. doi:10.1136/jmg.17.1.53 [Abstract] [PDF] [Request Permissions]

Familial caudal regression anomalad and maternal diabetes.
J Evans and A Hunter
J Med Genet 1980; 17: 57-58. doi:10.1136/jmg.17.1.57 [PDF] [Request Permissions]

Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome.
G Zamboni, F Bernardi, C Danesino, U M del Majno, G Beghini, and B Dalla Bernardina
J Med Genet 1980; 17: 59-61. doi:10.1136/jmg.17.1.59 [Abstract] [PDF] [Request Permissions]

47,XXX chromosome constitution in a male.
U Bigozzi, G Simoni, E Montali, L Dalpra, F Rossella, M Piazzini, and A Borghi
J Med Genet 1980; 17: 62-66. doi:10.1136/jmg.17.1.62 [Abstract] [PDF] [Request Permissions]

Complex chromosomal rearrangement leading to partial trisomy 22.
I L Hansteen, L Schirmer, S Hestetun, and A Brøgger
J Med Genet 1980; 17: 66-68. doi:10.1136/jmg.17.1.66 [Abstract] [PDF] [Request Permissions]

Concurrence of anorexia nervosa and yellow mutant albinism.
J T Kelly, J Rohde, C J Witkop, Jr, and A Johannes
J Med Genet 1980; 17: 68-71. doi:10.1136/jmg.17.1.68 [Abstract] [PDF] [Request Permissions]

Simultaneous G- and C- banding for human chromosomes.
R S Verma and H Dosik
J Med Genet 1980; 17: 72-73. doi:10.1136/jmg.17.1.72 [PDF] [Request Permissions]

Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism.
G R Sutherland, C G Judge, and S Wiener
J Med Genet 1980; 17: 73-74. doi:10.1136/jmg.17.1.73 [PDF] [Request Permissions]

Covesdem syndrome.
R M Winter
J Med Genet 1980; 17: 74-75. doi:10.1136/jmg.17.1.74 [PDF] [Request Permissions]

Dermatoglyphic findings in Laurence-Moon-Biedl syndrome.
M Atasu
J Med Genet 1980; 17: 75-76. doi:10.1136/jmg.17.1.75 [PDF] [Request Permissions]

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	Inbreeding effects on fetal growth and development P S S Rao and S G Inbaraj J Med Genet 1980; 17: 27-33. doi:10.1136/jmg.17.1.27 [Abstract] [PDF] [Request Permissions]

	Elemente der klinischen Genetik. Grundlagen und Anwendung der Humangenetik in Studium und Praxis Andrew P Read J Med Genet 1980; 17: 77. doi:10.1136/jmg.17.1.77 [PDF] [Request Permissions]

	Metabolic Disease in Childhood J V Leonard J Med Genet 1980; 17: 77-78. doi:10.1136/jmg.17.1.77-a [PDF] [Request Permissions]

	Human Genetics (Outline Studies in Biology) A W Johnston J Med Genet 1980; 17: 78-79. doi:10.1136/jmg.17.1.78 [PDF] [Request Permissions]

	Genetics and Cancer in Man D F Roberts J Med Genet 1980; 17: 79-80. doi:10.1136/jmg.17.1.79 [PDF] [Request Permissions]

	Chemical Mutagens. Principles and Methods for their Detection B A Bridges J Med Genet 1980; 17: 80. doi:10.1136/jmg.17.1.80 [PDF] [Request Permissions]

	Haems and chlorophylls: comparison of function and formation. G A Hendry and O T Jones J Med Genet 1980; 17: 1-14. doi:10.1136/jmg.17.1.1 [PDF] [Request Permissions]

	An overall genetic risk assessment for radiological protection purposes. P Oftedal and A G Searle J Med Genet 1980; 17: 15-20. doi:10.1136/jmg.17.1.15 [Abstract] [PDF] [Request Permissions]

	Angiokeratoma corporis diffusum with features of a mucopolysaccharidosis. D I McCallum, R F Macadam, and A W Johnston J Med Genet 1980; 17: 21-26. doi:10.1136/jmg.17.1.21 [Abstract] [PDF] [Request Permissions]

	Sickle cell disease in Sicily. E F Roth, Jr, G Schiliro, A Russo, S Musumeci, E Rachmilewitz, V Neske, and R Nagel J Med Genet 1980; 17: 34-38. doi:10.1136/jmg.17.1.34 [Abstract] [PDF] [Request Permissions]

	Dominant inheritance in a family with primary atrophic rhinitis. J R Sibert and R P Barton J Med Genet 1980; 17: 39-40. doi:10.1136/jmg.17.1.39 [Abstract] [PDF] [Request Permissions]

	Sex-influenced expression of Madelung's deformity in a family of dyschondrosteosis. J R Lichtenstein, M Sundaram, and R Burdge J Med Genet 1980; 17: 41-43. doi:10.1136/jmg.17.1.41 [Abstract] [PDF] [Request Permissions]

	High resolution of a small pericentric inversion of chromosome 11. H Autio-Harmainen and A De La Chapelle J Med Genet 1980; 17: 44-47. doi:10.1136/jmg.17.1.44 [Abstract] [PDF] [Request Permissions]

	Trisomy 21 mosaicism in two successive generations in a family. J C Parke, Jr, F S Grass, R Pixley, and J Deal J Med Genet 1980; 17: 48-49. doi:10.1136/jmg.17.1.48 [Abstract] [PDF] [Request Permissions]

	Dermatoglyphic findings in Poland's syndrome. M Atasu J Med Genet 1980; 17: 50-52. doi:10.1136/jmg.17.1.50 [Abstract] [PDF] [Request Permissions]

	Frontometaphyseal dysplasia: autosomal dominant or X-linked? P Beighton and H Hamersma J Med Genet 1980; 17: 53-56. doi:10.1136/jmg.17.1.53 [Abstract] [PDF] [Request Permissions]

	Familial caudal regression anomalad and maternal diabetes. J Evans and A Hunter J Med Genet 1980; 17: 57-58. doi:10.1136/jmg.17.1.57 [PDF] [Request Permissions]

	Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome. G Zamboni, F Bernardi, C Danesino, U M del Majno, G Beghini, and B Dalla Bernardina J Med Genet 1980; 17: 59-61. doi:10.1136/jmg.17.1.59 [Abstract] [PDF] [Request Permissions]

	47,XXX chromosome constitution in a male. U Bigozzi, G Simoni, E Montali, L Dalpra, F Rossella, M Piazzini, and A Borghi J Med Genet 1980; 17: 62-66. doi:10.1136/jmg.17.1.62 [Abstract] [PDF] [Request Permissions]

	Complex chromosomal rearrangement leading to partial trisomy 22. I L Hansteen, L Schirmer, S Hestetun, and A Brøgger J Med Genet 1980; 17: 66-68. doi:10.1136/jmg.17.1.66 [Abstract] [PDF] [Request Permissions]

	Concurrence of anorexia nervosa and yellow mutant albinism. J T Kelly, J Rohde, C J Witkop, Jr, and A Johannes J Med Genet 1980; 17: 68-71. doi:10.1136/jmg.17.1.68 [Abstract] [PDF] [Request Permissions]

	Simultaneous G- and C- banding for human chromosomes. R S Verma and H Dosik J Med Genet 1980; 17: 72-73. doi:10.1136/jmg.17.1.72 [PDF] [Request Permissions]

	Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism. G R Sutherland, C G Judge, and S Wiener J Med Genet 1980; 17: 73-74. doi:10.1136/jmg.17.1.73 [PDF] [Request Permissions]

	Covesdem syndrome. R M Winter J Med Genet 1980; 17: 74-75. doi:10.1136/jmg.17.1.74 [PDF] [Request Permissions]

	Dermatoglyphic findings in Laurence-Moon-Biedl syndrome. M Atasu J Med Genet 1980; 17: 75-76. doi:10.1136/jmg.17.1.75 [PDF] [Request Permissions]