J Med Genet -- Table of Contents (15 [3])

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June 1978 (Volume 15, Number 3). [Index by author]

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Articles

Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism
Lillian Y. F. Hsu, Sophie Paciuc, Karen David, Steluta Cristian, Ralph Moloshok, and Kurt Hirschhorn
J Med Genet 1978; 15: 222-226. doi:10.1136/jmg.15.3.222 [Abstract] [PDF] [Request Permissions]

Research Article

Parthenogenesis.
U Mittwoch
J Med Genet 1978; 15: 165-181. doi:10.1136/jmg.15.3.165 [PDF] [Request Permissions]

Inducibility of aryl hydrocarbon hydroxylase in cultured human lymphocytes: a study of repeatability.
K A Fletcher, D A Evans, and M V Canning
J Med Genet 1978; 15: 182-188. doi:10.1136/jmg.15.3.182 [Abstract] [PDF] [Request Permissions]

Hereditary pancreatitis in England and Wales.
J R Sibert
J Med Genet 1978; 15: 189-201. doi:10.1136/jmg.15.3.189 [Abstract] [PDF] [Request Permissions]

First premarital screening of thalassaemia carriers in intermediate schools in Latium.
E Silvestroni, I Bianco, B Graziani, C Carboni, and S U D'Arca
J Med Genet 1978; 15: 202-207. doi:10.1136/jmg.15.3.202 [Abstract] [PDF] [Request Permissions]

Brachydactyly, distal symphalangism, scoliosis, tall stature, and club feet: a new syndrome.
D O Sillence
J Med Genet 1978; 15: 208-211. doi:10.1136/jmg.15.3.208 [Abstract] [PDF] [Request Permissions]

Autosomal recessive postaxial polydactyly type A in a Sicilian family.
F Mollica, S L Volti, and G Sorge
J Med Genet 1978; 15: 212-216. doi:10.1136/jmg.15.3.212 [Abstract] [PDF] [Request Permissions]

Linkage studies in Van der Woude syndrome.
J R Eastman, D Bixler, and V Escobar
J Med Genet 1978; 15: 217-218. doi:10.1136/jmg.15.3.217 [Abstract] [PDF] [Request Permissions]

Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association.
S Bernasconi, C Pezzani, P Balestrazzi, and A Marbini
J Med Genet 1978; 15: 219-221. doi:10.1136/jmg.15.3.219 [Abstract] [PDF] [Request Permissions]

Necropsy of original case of Lowry's syndrome.
C L Dolman and V J Wright
J Med Genet 1978; 15: 227-229. doi:10.1136/jmg.15.3.227 [Abstract] [PDF] [Request Permissions]

Late discovery of a case of testicular feminisation.
A M Schindler and J Csank-Brassert
J Med Genet 1978; 15: 229-232. doi:10.1136/jmg.15.3.229 [Abstract] [PDF] [Request Permissions]

Inconsistent expression of both centromeres of a dicentric Y chromosome in a child with ambiguous external genitalia.
B Fass, S Kaplan, B Lippe, and R S Sparkes
J Med Genet 1978; 15: 232-236. doi:10.1136/jmg.15.3.232 [Abstract] [PDF] [Request Permissions]

Deletion 14q and pericentric inversion 14.
J Nielsen, A Homma, K Rasmussen, E Ried, K Sorensen, and P Saldana-Garcia
J Med Genet 1978; 15: 236-238. doi:10.1136/jmg.15.3.236 [Abstract] [PDF] [Request Permissions]

Acute myelogenous leukaemia in Hurler's syndrome.
K T Chen, R W McKenna, and R J Desnick
J Med Genet 1978; 15: 239-242. doi:10.1136/jmg.15.3.239 [Abstract] [PDF] [Request Permissions]

Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs.
Crawfurd MdA, P Jackson, and H G Kohler
J Med Genet 1978; 15: 242-245. doi:10.1136/jmg.15.3.242 [Abstract] [PDF] [Request Permissions]

Heterozygote advantage for the phenylketonuria allele.
I Smith, C O Carter, and O H Wolff
J Med Genet 1978; 15: 246-248. doi:10.1136/jmg.15.3.246 [PDF] [Request Permissions]

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	Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism Lillian Y. F. Hsu, Sophie Paciuc, Karen David, Steluta Cristian, Ralph Moloshok, and Kurt Hirschhorn J Med Genet 1978; 15: 222-226. doi:10.1136/jmg.15.3.222 [Abstract] [PDF] [Request Permissions]

	Parthenogenesis. U Mittwoch J Med Genet 1978; 15: 165-181. doi:10.1136/jmg.15.3.165 [PDF] [Request Permissions]

	Inducibility of aryl hydrocarbon hydroxylase in cultured human lymphocytes: a study of repeatability. K A Fletcher, D A Evans, and M V Canning J Med Genet 1978; 15: 182-188. doi:10.1136/jmg.15.3.182 [Abstract] [PDF] [Request Permissions]

	Hereditary pancreatitis in England and Wales. J R Sibert J Med Genet 1978; 15: 189-201. doi:10.1136/jmg.15.3.189 [Abstract] [PDF] [Request Permissions]

	First premarital screening of thalassaemia carriers in intermediate schools in Latium. E Silvestroni, I Bianco, B Graziani, C Carboni, and S U D'Arca J Med Genet 1978; 15: 202-207. doi:10.1136/jmg.15.3.202 [Abstract] [PDF] [Request Permissions]

	Brachydactyly, distal symphalangism, scoliosis, tall stature, and club feet: a new syndrome. D O Sillence J Med Genet 1978; 15: 208-211. doi:10.1136/jmg.15.3.208 [Abstract] [PDF] [Request Permissions]

	Autosomal recessive postaxial polydactyly type A in a Sicilian family. F Mollica, S L Volti, and G Sorge J Med Genet 1978; 15: 212-216. doi:10.1136/jmg.15.3.212 [Abstract] [PDF] [Request Permissions]

	Linkage studies in Van der Woude syndrome. J R Eastman, D Bixler, and V Escobar J Med Genet 1978; 15: 217-218. doi:10.1136/jmg.15.3.217 [Abstract] [PDF] [Request Permissions]

	Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association. S Bernasconi, C Pezzani, P Balestrazzi, and A Marbini J Med Genet 1978; 15: 219-221. doi:10.1136/jmg.15.3.219 [Abstract] [PDF] [Request Permissions]

	Necropsy of original case of Lowry's syndrome. C L Dolman and V J Wright J Med Genet 1978; 15: 227-229. doi:10.1136/jmg.15.3.227 [Abstract] [PDF] [Request Permissions]

	Late discovery of a case of testicular feminisation. A M Schindler and J Csank-Brassert J Med Genet 1978; 15: 229-232. doi:10.1136/jmg.15.3.229 [Abstract] [PDF] [Request Permissions]

	Inconsistent expression of both centromeres of a dicentric Y chromosome in a child with ambiguous external genitalia. B Fass, S Kaplan, B Lippe, and R S Sparkes J Med Genet 1978; 15: 232-236. doi:10.1136/jmg.15.3.232 [Abstract] [PDF] [Request Permissions]

	Deletion 14q and pericentric inversion 14. J Nielsen, A Homma, K Rasmussen, E Ried, K Sorensen, and P Saldana-Garcia J Med Genet 1978; 15: 236-238. doi:10.1136/jmg.15.3.236 [Abstract] [PDF] [Request Permissions]

	Acute myelogenous leukaemia in Hurler's syndrome. K T Chen, R W McKenna, and R J Desnick J Med Genet 1978; 15: 239-242. doi:10.1136/jmg.15.3.239 [Abstract] [PDF] [Request Permissions]

	Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs. Crawfurd MdA, P Jackson, and H G Kohler J Med Genet 1978; 15: 242-245. doi:10.1136/jmg.15.3.242 [Abstract] [PDF] [Request Permissions]

	Heterozygote advantage for the phenylketonuria allele. I Smith, C O Carter, and O H Wolff J Med Genet 1978; 15: 246-248. doi:10.1136/jmg.15.3.246 [PDF] [Request Permissions]