J Med Genet -- Table of Contents (13 [5])

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October 1976 (Volume 13, Number 5). [Index by author]

		Book Reviews Research Article

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Book Reviews

Genetic diversity among Australian Aborigines. (Australian Aboriginal Studies Research and Regional Studies No. 3.)
D. F. Roberts
J Med Genet 1976; 13: 413. doi:10.1136/jmg.13.5.413 [PDF] [Request Permissions]

Chromosome Variations in Human Evolution
C. E. Blank
J Med Genet 1976; 13: 413-414. doi:10.1136/jmg.13.5.413-a [PDF] [Request Permissions]

Chromosome Hierarchy. An Introduction to the Biology of the Chromosome
A. McDermott
J Med Genet 1976; 13: 414. doi:10.1136/jmg.13.5.414 [PDF] [Request Permissions]

Chromosomal Variation in Man. A Catalog of Chromosomal Variants and Anomalies
Michael Baraitser
J Med Genet 1976; 13: 414-415. doi:10.1136/jmg.13.5.414-a [PDF] [Request Permissions]

New Chromosomal and Malformation Syndromes
Michael Baraitser
J Med Genet 1976; 13: 415. doi:10.1136/jmg.13.5.415 [PDF] [Request Permissions]

Familial Polyposis Coli. Family Studies, Histopathology, Differential Diagnosis, and Results of Treatment
R. B. McConnell
J Med Genet 1976; 13: 415-416. doi:10.1136/jmg.13.5.415-a [PDF] [Request Permissions]

Human Malformations. British Medical Bulletin. Vol. 32, No. 1
Alan E. H. Emery
J Med Genet 1976; 13: 416. doi:10.1136/jmg.13.5.416 [PDF] [Request Permissions]

Handbook of Hemophilia, Parts I and II
F. G. H. Hill
J Med Genet 1976; 13: 416. doi:10.1136/jmg.13.5.416-a [PDF] [Request Permissions]

Research Article

Genetic polymorphism and interethnic variability of plasma paroxonase activity.
J R Playfer, L C Eze, M F Bullen, and D A Evans
J Med Genet 1976; 13: 337-342. doi:10.1136/jmg.13.5.337 [Abstract] [PDF] [Request Permissions]

Spinal dysraphism: genetic relation to neural tube malformations.
C O Carter, K A Evans, and K Till
J Med Genet 1976; 13: 343-350. doi:10.1136/jmg.13.5.343 [Abstract] [PDF] [Request Permissions]

Risks of miscarriage after amniocentesis.
C O Carter
J Med Genet 1976; 13: 351. doi:10.1136/jmg.13.5.351 [PDF] [Request Permissions]

An unusual family of benign "X" linked muscular dystrophy with cardiac involvement.
R S Wadia, S U Wadgaonkar, R B Amin, and H V Sardesai
J Med Genet 1976; 13: 352-356. doi:10.1136/jmg.13.5.352 [Abstract] [PDF] [Request Permissions]

Familial essential ("benign") chorea.
T D Bird, C B Carlson, and J G Hall
J Med Genet 1976; 13: 357-362. doi:10.1136/jmg.13.5.357 [Abstract] [PDF] [Request Permissions]

Haemoglobin LeporeBoston in a Turkish family.
A O Cavdar and A Arcasoy
J Med Genet 1976; 13: 363-365. doi:10.1136/jmg.13.5.363 [Abstract] [PDF] [Request Permissions]

Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.
A M Vianna-Morgante, M J Nozaki, C C Ortega, V Coates, and Y Yamamura
J Med Genet 1976; 13: 366-370. doi:10.1136/jmg.13.5.366 [Abstract] [PDF] [Request Permissions]

Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man.
C M Gosden, M O Wright, W G Paterson, and K A Grant
J Med Genet 1976; 13: 371-380. doi:10.1136/jmg.13.5.371 [Abstract] [PDF] [Request Permissions]

Structure and inheritance of some heterozygous Robertsonian translocation in man.
A Daniel and P R Lam-Po-Tang
J Med Genet 1976; 13: 381-388. doi:10.1136/jmg.13.5.381 [Abstract] [PDF] [Request Permissions]

Association of D/D translocations with fetal wastage and aneuploidy. A report of four families.
P M Fernhoff, D N Singh, J Hanson, S Trusler, C R Dumont, and A T Chen
J Med Genet 1976; 13: 389-393. doi:10.1136/jmg.13.5.389 [Abstract] [PDF] [Request Permissions]

Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritis.
V Ventruto, R Di Girlamo, B Festa, A Romano, G Sebastio, and L Sebastio
J Med Genet 1976; 13: 394-398. doi:10.1136/jmg.13.5.394 [Abstract] [PDF] [Request Permissions]

Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groups.
C J de Weerdt
J Med Genet 1976; 13: 399. doi:10.1136/jmg.13.5.399 [Abstract] [PDF] [Request Permissions]

Antenatal diagnosis of trisomy 13 with unexpected increase in alpha-feto protein.
J S Fitzsimmons, G M Filshie, A S Hill, and R Kime
J Med Genet 1976; 13: 400-402. doi:10.1136/jmg.13.5.400 [Abstract] [PDF] [Request Permissions]

Discordance for Cornelia de Lange syndrome in twins.
R E Stevenson and C I Scott, Jr
J Med Genet 1976; 13: 402-404. doi:10.1136/jmg.13.5.402 [Abstract] [PDF] [Request Permissions]

The de Lange syndrome in one of twins.
G Carakushannsky and C Berthier
J Med Genet 1976; 13: 404-406. doi:10.1136/jmg.13.5.404 [Abstract] [PDF] [Request Permissions]

Gardner's syndrome and steatocystoma multiplex. Two unusual genetically determined conditions occurring in same patient.
B Leppard and H R Thompson
J Med Genet 1976; 13: 407-411. doi:10.1136/jmg.13.5.407 [Abstract] [PDF] [Request Permissions]

A giant short arm of no. 21 chromosome in mother of 21/21 translocation mongol.
E Tuncbilek, M Bobrow, G Clarke, and K Taysi
J Med Genet 1976; 13: 411-412. doi:10.1136/jmg.13.5.411 [Abstract] [PDF] [Request Permissions]

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	Genetic diversity among Australian Aborigines. (Australian Aboriginal Studies Research and Regional Studies No. 3.) D. F. Roberts J Med Genet 1976; 13: 413. doi:10.1136/jmg.13.5.413 [PDF] [Request Permissions]

	Chromosome Variations in Human Evolution C. E. Blank J Med Genet 1976; 13: 413-414. doi:10.1136/jmg.13.5.413-a [PDF] [Request Permissions]

	Chromosome Hierarchy. An Introduction to the Biology of the Chromosome A. McDermott J Med Genet 1976; 13: 414. doi:10.1136/jmg.13.5.414 [PDF] [Request Permissions]

	Chromosomal Variation in Man. A Catalog of Chromosomal Variants and Anomalies Michael Baraitser J Med Genet 1976; 13: 414-415. doi:10.1136/jmg.13.5.414-a [PDF] [Request Permissions]

	New Chromosomal and Malformation Syndromes Michael Baraitser J Med Genet 1976; 13: 415. doi:10.1136/jmg.13.5.415 [PDF] [Request Permissions]

	Familial Polyposis Coli. Family Studies, Histopathology, Differential Diagnosis, and Results of Treatment R. B. McConnell J Med Genet 1976; 13: 415-416. doi:10.1136/jmg.13.5.415-a [PDF] [Request Permissions]

	Human Malformations. British Medical Bulletin. Vol. 32, No. 1 Alan E. H. Emery J Med Genet 1976; 13: 416. doi:10.1136/jmg.13.5.416 [PDF] [Request Permissions]

	Handbook of Hemophilia, Parts I and II F. G. H. Hill J Med Genet 1976; 13: 416. doi:10.1136/jmg.13.5.416-a [PDF] [Request Permissions]

	Genetic polymorphism and interethnic variability of plasma paroxonase activity. J R Playfer, L C Eze, M F Bullen, and D A Evans J Med Genet 1976; 13: 337-342. doi:10.1136/jmg.13.5.337 [Abstract] [PDF] [Request Permissions]

	Spinal dysraphism: genetic relation to neural tube malformations. C O Carter, K A Evans, and K Till J Med Genet 1976; 13: 343-350. doi:10.1136/jmg.13.5.343 [Abstract] [PDF] [Request Permissions]

	Risks of miscarriage after amniocentesis. C O Carter J Med Genet 1976; 13: 351. doi:10.1136/jmg.13.5.351 [PDF] [Request Permissions]

	An unusual family of benign "X" linked muscular dystrophy with cardiac involvement. R S Wadia, S U Wadgaonkar, R B Amin, and H V Sardesai J Med Genet 1976; 13: 352-356. doi:10.1136/jmg.13.5.352 [Abstract] [PDF] [Request Permissions]

	Familial essential ("benign") chorea. T D Bird, C B Carlson, and J G Hall J Med Genet 1976; 13: 357-362. doi:10.1136/jmg.13.5.357 [Abstract] [PDF] [Request Permissions]

	Haemoglobin LeporeBoston in a Turkish family. A O Cavdar and A Arcasoy J Med Genet 1976; 13: 363-365. doi:10.1136/jmg.13.5.363 [Abstract] [PDF] [Request Permissions]

	Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18. A M Vianna-Morgante, M J Nozaki, C C Ortega, V Coates, and Y Yamamura J Med Genet 1976; 13: 366-370. doi:10.1136/jmg.13.5.366 [Abstract] [PDF] [Request Permissions]

	Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in man. C M Gosden, M O Wright, W G Paterson, and K A Grant J Med Genet 1976; 13: 371-380. doi:10.1136/jmg.13.5.371 [Abstract] [PDF] [Request Permissions]

	Structure and inheritance of some heterozygous Robertsonian translocation in man. A Daniel and P R Lam-Po-Tang J Med Genet 1976; 13: 381-388. doi:10.1136/jmg.13.5.381 [Abstract] [PDF] [Request Permissions]

	Association of D/D translocations with fetal wastage and aneuploidy. A report of four families. P M Fernhoff, D N Singh, J Hanson, S Trusler, C R Dumont, and A T Chen J Med Genet 1976; 13: 389-393. doi:10.1136/jmg.13.5.389 [Abstract] [PDF] [Request Permissions]

	Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritis. V Ventruto, R Di Girlamo, B Festa, A Romano, G Sebastio, and L Sebastio J Med Genet 1976; 13: 394-398. doi:10.1136/jmg.13.5.394 [Abstract] [PDF] [Request Permissions]

	Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groups. C J de Weerdt J Med Genet 1976; 13: 399. doi:10.1136/jmg.13.5.399 [Abstract] [PDF] [Request Permissions]

	Antenatal diagnosis of trisomy 13 with unexpected increase in alpha-feto protein. J S Fitzsimmons, G M Filshie, A S Hill, and R Kime J Med Genet 1976; 13: 400-402. doi:10.1136/jmg.13.5.400 [Abstract] [PDF] [Request Permissions]

	Discordance for Cornelia de Lange syndrome in twins. R E Stevenson and C I Scott, Jr J Med Genet 1976; 13: 402-404. doi:10.1136/jmg.13.5.402 [Abstract] [PDF] [Request Permissions]

	The de Lange syndrome in one of twins. G Carakushannsky and C Berthier J Med Genet 1976; 13: 404-406. doi:10.1136/jmg.13.5.404 [Abstract] [PDF] [Request Permissions]

	Gardner's syndrome and steatocystoma multiplex. Two unusual genetically determined conditions occurring in same patient. B Leppard and H R Thompson J Med Genet 1976; 13: 407-411. doi:10.1136/jmg.13.5.407 [Abstract] [PDF] [Request Permissions]

	A giant short arm of no. 21 chromosome in mother of 21/21 translocation mongol. E Tuncbilek, M Bobrow, G Clarke, and K Taysi J Med Genet 1976; 13: 411-412. doi:10.1136/jmg.13.5.411 [Abstract] [PDF] [Request Permissions]