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March 1991 (Volume 28, Number 3). [Index by author]

		Book Reviews Conference Report Research Article

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Book Reviews

Advances in Human Genetics
I D Young
J Med Genet 1991; 28: 215. doi:10.1136/jmg.28.3.215 [PDF] [Request Permissions]

Human Achondroplasia—A Multi-disciplinary Approach
Ruth Wynne Davies
J Med Genet 1991; 28: 215-216. doi:10.1136/jmg.28.3.215-a [PDF] [Request Permissions]

Epidermolysis Bullosa: A Comprehensive Review of Classification, Management and Laboratory Studies
Andrew Y Finlay
J Med Genet 1991; 28: 216. doi:10.1136/jmg.28.3.216 [PDF] [Request Permissions]

Conference Report

The genetics, demography, and health of minority populations: a symposium held by The Galton Institute, September 1990
Sarah Bundey
J Med Genet 1991; 28: 211-212. doi:10.1136/jmg.28.3.211 [PDF] [Request Permissions]

Research Article

Prenatal diagnosis of osteogenesis imperfecta by identification of the concordant collagen 1 allele.
J R Lynch, D Ogilvie, L Priestley, C Baigrie, R Smith, P Farndon, and B Sykes
J Med Genet 1991; 28: 145-150. doi:10.1136/jmg.28.3.145 [Abstract] [PDF] [Request Permissions]

A cytogenetic and molecular study of a series of 45,X fetuses and their parents.
A Cockwell, M MacKenzie, S Youings, and P Jacobs
J Med Genet 1991; 28: 151-155. doi:10.1136/jmg.28.3.151 [Abstract] [PDF] [Request Permissions]

Analysis of the origin of Turner's syndrome using polymorphic DNA probes.
S A Loughlin, A Redha, J McIver, E Boyd, A Carothers, and J M Connor
J Med Genet 1991; 28: 156-158. doi:10.1136/jmg.28.3.156 [Abstract] [PDF] [Request Permissions]

Molecular studies of non-disjunction in trisomy 16.
T J Hassold, D Pettay, S B Freeman, M Grantham, and N Takaesu
J Med Genet 1991; 28: 159-162. doi:10.1136/jmg.28.3.159 [Abstract] [PDF] [Request Permissions]

Molecular and cytogenetic analysis of a familial microdeletion of Xq.
S Wells, S Mould, D Robins, D Robinson, and P Jacobs
J Med Genet 1991; 28: 163-166. doi:10.1136/jmg.28.3.163 [Abstract] [PDF] [Request Permissions]

Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.
Y T Zeng, M J Chen, Z R Ren, X K Qui, and S Z Huang
J Med Genet 1991; 28: 167-170. doi:10.1136/jmg.28.3.167 [Abstract] [PDF] [Request Permissions]

Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians.
N S Van-de-Water, D Ridgway, and P A Ockelford
J Med Genet 1991; 28: 171-176. doi:10.1136/jmg.28.3.171 [Abstract] [PDF] [Request Permissions]

Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish population.
E C Landels, I H Ellis, A H Fensom, P M Green, and M Bobrow
J Med Genet 1991; 28: 177-180. doi:10.1136/jmg.28.3.177 [Abstract] [PDF] [Request Permissions]

Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.
P J Crawford, M J Aldred, and A Clarke
J Med Genet 1991; 28: 181-185. doi:10.1136/jmg.28.3.181 [Abstract] [PDF] [Request Permissions]

Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome.
M Le Merrer, R Brauner, and P Maroteaux
J Med Genet 1991; 28: 186-191. doi:10.1136/jmg.28.3.186 [Abstract] [PDF] [Request Permissions]

The acetylator phenotypes of Saudi Arabians with coronary arterial atheroma.
D A Evans, J Wicks, J Higgins, and M Assisto
J Med Genet 1991; 28: 192-193. doi:10.1136/jmg.28.3.192 [Abstract] [PDF] [Request Permissions]

Analysis of problems in making the reproductive decision after genetic counselling.
P G Frets, H J Duivenvoorden, F Verhage, B M Peters-Romeyn, and M F Niermeijer
J Med Genet 1991; 28: 194-200. doi:10.1136/jmg.28.3.194 [Abstract] [PDF] [Request Permissions]

Floating-Harbor syndrome.
M A Patton, J Hurst, D Donnai, C M McKeown, T Cole, and J Goodship
J Med Genet 1991; 28: 201-204. doi:10.1136/jmg.28.3.201 [PDF] [Request Permissions]

A new case of proximal 10q partial trisomy.
M I de Michelena and P J Campos
J Med Genet 1991; 28: 205-206. doi:10.1136/jmg.28.3.205 [Abstract] [PDF] [Request Permissions]

The CHARGE association and athyreosis.
J F Marín, B García, A Quintana, R Barrio, M T Sordo, and C Lozano
J Med Genet 1991; 28: 207-208. doi:10.1136/jmg.28.3.207 [Abstract] [PDF] [Request Permissions]

DMD carrier detection in a female with mosaic Turner's syndrome.
M Baiget, E Tizzano, V Volpini, E del Rio, T Pérez-Vidal, and P Gallano
J Med Genet 1991; 28: 209-210. doi:10.1136/jmg.28.3.209 [PDF] [Request Permissions]

Male proband with X linked retinoschisis apparently inherited from his father's family.
M S Newton, S Collyer, and C I Phillips
J Med Genet 1991; 28: 213-214. doi:10.1136/jmg.28.3.213 [PDF] [Request Permissions]

Child naevus is not ILVEN.
R Happle
J Med Genet 1991; 28: 214. doi:10.1136/jmg.28.3.214 [PDF] [Request Permissions]

The variable clinical spectrum and mental prognosis of the acrocallosal syndrome.
J P Fryns, A Spaepen, C Grubben, H van den Berghe, and P Casaer
J Med Genet 1991; 28: 214-215. doi:10.1136/jmg.28.3.214-a [PDF] [Request Permissions]

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	Advances in Human Genetics I D Young J Med Genet 1991; 28: 215. doi:10.1136/jmg.28.3.215 [PDF] [Request Permissions]

	Human Achondroplasia—A Multi-disciplinary Approach Ruth Wynne Davies J Med Genet 1991; 28: 215-216. doi:10.1136/jmg.28.3.215-a [PDF] [Request Permissions]

	Epidermolysis Bullosa: A Comprehensive Review of Classification, Management and Laboratory Studies Andrew Y Finlay J Med Genet 1991; 28: 216. doi:10.1136/jmg.28.3.216 [PDF] [Request Permissions]

	The genetics, demography, and health of minority populations: a symposium held by The Galton Institute, September 1990 Sarah Bundey J Med Genet 1991; 28: 211-212. doi:10.1136/jmg.28.3.211 [PDF] [Request Permissions]

	Prenatal diagnosis of osteogenesis imperfecta by identification of the concordant collagen 1 allele. J R Lynch, D Ogilvie, L Priestley, C Baigrie, R Smith, P Farndon, and B Sykes J Med Genet 1991; 28: 145-150. doi:10.1136/jmg.28.3.145 [Abstract] [PDF] [Request Permissions]

	A cytogenetic and molecular study of a series of 45,X fetuses and their parents. A Cockwell, M MacKenzie, S Youings, and P Jacobs J Med Genet 1991; 28: 151-155. doi:10.1136/jmg.28.3.151 [Abstract] [PDF] [Request Permissions]

	Analysis of the origin of Turner's syndrome using polymorphic DNA probes. S A Loughlin, A Redha, J McIver, E Boyd, A Carothers, and J M Connor J Med Genet 1991; 28: 156-158. doi:10.1136/jmg.28.3.156 [Abstract] [PDF] [Request Permissions]

	Molecular studies of non-disjunction in trisomy 16. T J Hassold, D Pettay, S B Freeman, M Grantham, and N Takaesu J Med Genet 1991; 28: 159-162. doi:10.1136/jmg.28.3.159 [Abstract] [PDF] [Request Permissions]

	Molecular and cytogenetic analysis of a familial microdeletion of Xq. S Wells, S Mould, D Robins, D Robinson, and P Jacobs J Med Genet 1991; 28: 163-166. doi:10.1136/jmg.28.3.163 [Abstract] [PDF] [Request Permissions]

	Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene. Y T Zeng, M J Chen, Z R Ren, X K Qui, and S Z Huang J Med Genet 1991; 28: 167-170. doi:10.1136/jmg.28.3.167 [Abstract] [PDF] [Request Permissions]

	Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians. N S Van-de-Water, D Ridgway, and P A Ockelford J Med Genet 1991; 28: 171-176. doi:10.1136/jmg.28.3.171 [Abstract] [PDF] [Request Permissions]

	Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish population. E C Landels, I H Ellis, A H Fensom, P M Green, and M Bobrow J Med Genet 1991; 28: 177-180. doi:10.1136/jmg.28.3.177 [Abstract] [PDF] [Request Permissions]

	Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia. P J Crawford, M J Aldred, and A Clarke J Med Genet 1991; 28: 181-185. doi:10.1136/jmg.28.3.181 [Abstract] [PDF] [Request Permissions]

	Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome. M Le Merrer, R Brauner, and P Maroteaux J Med Genet 1991; 28: 186-191. doi:10.1136/jmg.28.3.186 [Abstract] [PDF] [Request Permissions]

	The acetylator phenotypes of Saudi Arabians with coronary arterial atheroma. D A Evans, J Wicks, J Higgins, and M Assisto J Med Genet 1991; 28: 192-193. doi:10.1136/jmg.28.3.192 [Abstract] [PDF] [Request Permissions]

	Analysis of problems in making the reproductive decision after genetic counselling. P G Frets, H J Duivenvoorden, F Verhage, B M Peters-Romeyn, and M F Niermeijer J Med Genet 1991; 28: 194-200. doi:10.1136/jmg.28.3.194 [Abstract] [PDF] [Request Permissions]

	Floating-Harbor syndrome. M A Patton, J Hurst, D Donnai, C M McKeown, T Cole, and J Goodship J Med Genet 1991; 28: 201-204. doi:10.1136/jmg.28.3.201 [PDF] [Request Permissions]

	A new case of proximal 10q partial trisomy. M I de Michelena and P J Campos J Med Genet 1991; 28: 205-206. doi:10.1136/jmg.28.3.205 [Abstract] [PDF] [Request Permissions]

	The CHARGE association and athyreosis. J F Marín, B García, A Quintana, R Barrio, M T Sordo, and C Lozano J Med Genet 1991; 28: 207-208. doi:10.1136/jmg.28.3.207 [Abstract] [PDF] [Request Permissions]

	DMD carrier detection in a female with mosaic Turner's syndrome. M Baiget, E Tizzano, V Volpini, E del Rio, T Pérez-Vidal, and P Gallano J Med Genet 1991; 28: 209-210. doi:10.1136/jmg.28.3.209 [PDF] [Request Permissions]

	Male proband with X linked retinoschisis apparently inherited from his father's family. M S Newton, S Collyer, and C I Phillips J Med Genet 1991; 28: 213-214. doi:10.1136/jmg.28.3.213 [PDF] [Request Permissions]

	Child naevus is not ILVEN. R Happle J Med Genet 1991; 28: 214. doi:10.1136/jmg.28.3.214 [PDF] [Request Permissions]

	The variable clinical spectrum and mental prognosis of the acrocallosal syndrome. J P Fryns, A Spaepen, C Grubben, H van den Berghe, and P Casaer J Med Genet 1991; 28: 214-215. doi:10.1136/jmg.28.3.214-a [PDF] [Request Permissions]