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April 1988 (Volume 25, Number 4). [Index by author]

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Book Reviews

Genetic Disease: Screening and Management
R F Mueller
J Med Genet 1988; 25: 284. doi:10.1136/jmg.25.4.284 [PDF] [Request Permissions]

Monoclonals and DNA Probes in Diagnostic and Preventive Medicine
Veronica Van Heyningen
J Med Genet 1988; 25: 284-285. doi:10.1136/jmg.25.4.284-a [PDF] [Request Permissions]

The Balance of Improbabilities: A Scientific Life
Alan E H Emery
J Med Genet 1988; 25: 285. doi:10.1136/jmg.25.4.285 [PDF] [Request Permissions]

Advances in Human Genetics
Thaddeus E Kelly
J Med Genet 1988; 25: 285-286. doi:10.1136/jmg.25.4.285-a [PDF] [Request Permissions]

Prenatal Diagnosis of Heritable Skin Diseases
A Y Finlay
J Med Genet 1988; 25: 286. doi:10.1136/jmg.25.4.286 [PDF] [Request Permissions]

The Correspondence of Charles Darwin
Peter S Harper
J Med Genet 1988; 25: 286-287. doi:10.1136/jmg.25.4.286-a [PDF] [Request Permissions]

Chorion Villus Sampling
I Rocker
J Med Genet 1988; 25: 287. doi:10.1136/jmg.25.4.287 [PDF] [Request Permissions]

Research Article

Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.
V Greger, S Kerst, E Messmer, W Höpping, E Passarge, and B Horsthemke
J Med Genet 1988; 25: 217-221. doi:10.1136/jmg.25.4.217 [Abstract] [PDF] [Request Permissions]

Linkage analysis of X linked retinitis pigmentosa in the Irish population.
G J Farrar, M T Geraghty, J M Moloney, D J McConnell, and P Humphries
J Med Genet 1988; 25: 222-226. doi:10.1136/jmg.25.4.222 [Abstract] [PDF] [Request Permissions]

A family showing apparent X linked inheritance of both anencephaly and spina bifida.
O Jensson, A Arnason, H Gunnarsdottir, I Petursdottir, R Fossdal, and S Hreidarsson
J Med Genet 1988; 25: 227-229. doi:10.1136/jmg.25.4.227 [Abstract] [PDF] [Request Permissions]

Autosomal recessive inheritance of Nager acrofacial dysostosis.
J Chemke, B M Mogilner, I Ben-Itzhak, L Zurkowski, and D Ophir
J Med Genet 1988; 25: 230-232. doi:10.1136/jmg.25.4.230 [Abstract] [PDF] [Request Permissions]

Familial polyposis coli: no evidence for increased sensitivity to mitomycin C.
H A Mazzullo, J Attwood, and J D Delhanty
J Med Genet 1988; 25: 233-237. doi:10.1136/jmg.25.4.233 [Abstract] [PDF] [Request Permissions]

Expression of fra(10)(q25) in peripheral blood and bone marrow in familial neutropenia.
J A Holmes and P W Thompson
J Med Genet 1988; 25: 238-242. doi:10.1136/jmg.25.4.238 [Abstract] [PDF] [Request Permissions]

Theoretical recurrence risks for cleft lip derived from a population of consecutive newborns.
R Tenconi, M Clementi, and L Turolla
J Med Genet 1988; 25: 243-246. doi:10.1136/jmg.25.4.243 [Abstract] [PDF] [Request Permissions]

Hypothyroidism and sex chromosomes.
C Sarri, G B Côté, C Mengreli, I Lambadaridis, and S Pantelakis
J Med Genet 1988; 25: 247-249. doi:10.1136/jmg.25.4.247 [Abstract] [PDF] [Request Permissions]

Klippel-Trenaunay-Weber syndrome (angio-osteohypertrophy syndrome).
D L Viljoen
J Med Genet 1988; 25: 250-252. doi:10.1136/jmg.25.4.250 [PDF] [Request Permissions]

Medical genetics in China.
L Hui-Yuan
J Med Genet 1988; 25: 253-257. doi:10.1136/jmg.25.4.253 [PDF] [Request Permissions]

Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome.
A Serotkin, J Stamberg, and L Waber
J Med Genet 1988; 25: 258-260. doi:10.1136/jmg.25.4.258 [Abstract] [PDF] [Request Permissions]

De novo partial trisomy 15q (proximal type).
T J Herweijer, J W Oorthuys, and N J Leschot
J Med Genet 1988; 25: 260-262. doi:10.1136/jmg.25.4.260 [Abstract] [PDF] [Request Permissions]

Clinical consequences of deletion 1p35.
S L Wenger, M W Steele, and D J Becker
J Med Genet 1988; 25: 263. doi:10.1136/jmg.25.4.263 [Abstract] [PDF] [Request Permissions]

A duplication/deficient X chromosome in a girl with mental retardation and dysmorphic features.
I C Barnes, D Curtis, and S L Duncan
J Med Genet 1988; 25: 264-267. doi:10.1136/jmg.25.4.264 [Abstract] [PDF] [Request Permissions]

Martsolf's syndrome in a non-Jewish boy.
P Strisciuglio, M Costabile, M Esposito, and S Di Maio
J Med Genet 1988; 25: 267-269. doi:10.1136/jmg.25.4.267 [Abstract] [PDF] [Request Permissions]

Unknown syndrome: mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip.
C Garrett and J H Tripp
J Med Genet 1988; 25: 270-272. doi:10.1136/jmg.25.4.270 [Abstract] [PDF] [Request Permissions]

Unknown syndrome: microcephaly, facial clefting, and preaxial polydactyly.
F M Howard and I D Young
J Med Genet 1988; 25: 272-273. doi:10.1136/jmg.25.4.272 [Abstract] [PDF] [Request Permissions]

Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group)
J Med Genet 1988; 25: 274-283. doi:10.1136/jmg.25.4.274 [PDF] [Request Permissions]

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	Genetic Disease: Screening and Management R F Mueller J Med Genet 1988; 25: 284. doi:10.1136/jmg.25.4.284 [PDF] [Request Permissions]

	Monoclonals and DNA Probes in Diagnostic and Preventive Medicine Veronica Van Heyningen J Med Genet 1988; 25: 284-285. doi:10.1136/jmg.25.4.284-a [PDF] [Request Permissions]

	The Balance of Improbabilities: A Scientific Life Alan E H Emery J Med Genet 1988; 25: 285. doi:10.1136/jmg.25.4.285 [PDF] [Request Permissions]

	Advances in Human Genetics Thaddeus E Kelly J Med Genet 1988; 25: 285-286. doi:10.1136/jmg.25.4.285-a [PDF] [Request Permissions]

	Prenatal Diagnosis of Heritable Skin Diseases A Y Finlay J Med Genet 1988; 25: 286. doi:10.1136/jmg.25.4.286 [PDF] [Request Permissions]

	The Correspondence of Charles Darwin Peter S Harper J Med Genet 1988; 25: 286-287. doi:10.1136/jmg.25.4.286-a [PDF] [Request Permissions]

	Chorion Villus Sampling I Rocker J Med Genet 1988; 25: 287. doi:10.1136/jmg.25.4.287 [PDF] [Request Permissions]

	Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma. V Greger, S Kerst, E Messmer, W Höpping, E Passarge, and B Horsthemke J Med Genet 1988; 25: 217-221. doi:10.1136/jmg.25.4.217 [Abstract] [PDF] [Request Permissions]

	Linkage analysis of X linked retinitis pigmentosa in the Irish population. G J Farrar, M T Geraghty, J M Moloney, D J McConnell, and P Humphries J Med Genet 1988; 25: 222-226. doi:10.1136/jmg.25.4.222 [Abstract] [PDF] [Request Permissions]

	A family showing apparent X linked inheritance of both anencephaly and spina bifida. O Jensson, A Arnason, H Gunnarsdottir, I Petursdottir, R Fossdal, and S Hreidarsson J Med Genet 1988; 25: 227-229. doi:10.1136/jmg.25.4.227 [Abstract] [PDF] [Request Permissions]

	Autosomal recessive inheritance of Nager acrofacial dysostosis. J Chemke, B M Mogilner, I Ben-Itzhak, L Zurkowski, and D Ophir J Med Genet 1988; 25: 230-232. doi:10.1136/jmg.25.4.230 [Abstract] [PDF] [Request Permissions]

	Familial polyposis coli: no evidence for increased sensitivity to mitomycin C. H A Mazzullo, J Attwood, and J D Delhanty J Med Genet 1988; 25: 233-237. doi:10.1136/jmg.25.4.233 [Abstract] [PDF] [Request Permissions]

	Expression of fra(10)(q25) in peripheral blood and bone marrow in familial neutropenia. J A Holmes and P W Thompson J Med Genet 1988; 25: 238-242. doi:10.1136/jmg.25.4.238 [Abstract] [PDF] [Request Permissions]

	Theoretical recurrence risks for cleft lip derived from a population of consecutive newborns. R Tenconi, M Clementi, and L Turolla J Med Genet 1988; 25: 243-246. doi:10.1136/jmg.25.4.243 [Abstract] [PDF] [Request Permissions]

	Hypothyroidism and sex chromosomes. C Sarri, G B Côté, C Mengreli, I Lambadaridis, and S Pantelakis J Med Genet 1988; 25: 247-249. doi:10.1136/jmg.25.4.247 [Abstract] [PDF] [Request Permissions]

	Klippel-Trenaunay-Weber syndrome (angio-osteohypertrophy syndrome). D L Viljoen J Med Genet 1988; 25: 250-252. doi:10.1136/jmg.25.4.250 [PDF] [Request Permissions]

	Medical genetics in China. L Hui-Yuan J Med Genet 1988; 25: 253-257. doi:10.1136/jmg.25.4.253 [PDF] [Request Permissions]

	Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome. A Serotkin, J Stamberg, and L Waber J Med Genet 1988; 25: 258-260. doi:10.1136/jmg.25.4.258 [Abstract] [PDF] [Request Permissions]

	De novo partial trisomy 15q (proximal type). T J Herweijer, J W Oorthuys, and N J Leschot J Med Genet 1988; 25: 260-262. doi:10.1136/jmg.25.4.260 [Abstract] [PDF] [Request Permissions]

	Clinical consequences of deletion 1p35. S L Wenger, M W Steele, and D J Becker J Med Genet 1988; 25: 263. doi:10.1136/jmg.25.4.263 [Abstract] [PDF] [Request Permissions]

	A duplication/deficient X chromosome in a girl with mental retardation and dysmorphic features. I C Barnes, D Curtis, and S L Duncan J Med Genet 1988; 25: 264-267. doi:10.1136/jmg.25.4.264 [Abstract] [PDF] [Request Permissions]

	Martsolf's syndrome in a non-Jewish boy. P Strisciuglio, M Costabile, M Esposito, and S Di Maio J Med Genet 1988; 25: 267-269. doi:10.1136/jmg.25.4.267 [Abstract] [PDF] [Request Permissions]

	Unknown syndrome: mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip. C Garrett and J H Tripp J Med Genet 1988; 25: 270-272. doi:10.1136/jmg.25.4.270 [Abstract] [PDF] [Request Permissions]

	Unknown syndrome: microcephaly, facial clefting, and preaxial polydactyly. F M Howard and I D Young J Med Genet 1988; 25: 272-273. doi:10.1136/jmg.25.4.272 [Abstract] [PDF] [Request Permissions]

	Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group) J Med Genet 1988; 25: 274-283. doi:10.1136/jmg.25.4.274 [PDF] [Request Permissions]