J Med Genet -- Table of Contents (22 [5])

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October 1985 (Volume 22, Number 5). [Index by author]

		Obituaries Miscellaneous Correspondence Research Article

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Obituaries

Stanley Walker, BSc, PhD
Nina M Gregson
J Med Genet 1985; 22: 416. doi:10.1136/jmg.22.5.416 [PDF] [Request Permissions]

Miscellaneous

Correction
J Med Genet 1985; 22: 389. doi:10.1136/jmg.22.5.389 [PDF] [Request Permissions]

Correspondence

Correspondence
M J Seller and N C Nevin
J Med Genet 1985; 22: 412-413. doi:10.1136/jmg.22.5.412 [PDF] [Request Permissions]

Research Article

The human Y chromosome.
P Goodfellow, S Darling, and J Wolfe
J Med Genet 1985; 22: 329-344. doi:10.1136/jmg.22.5.329 [Abstract] [PDF] [Request Permissions]

Classroom teaching in genetics and birth defects: the Nottingham experience.
J S Fitzsimmons
J Med Genet 1985; 22: 345-349. doi:10.1136/jmg.22.5.345 [Abstract] [PDF] [Request Permissions]

Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.
I Hausmanowa-Petrusewicz, J Zaremba, and J Borkowska
J Med Genet 1985; 22: 350-353. doi:10.1136/jmg.22.5.350 [Abstract] [PDF] [Request Permissions]

Genetics and biochemical variability of variants of 21 hydroxylase deficiency.
M T Gordon, D I Conway, D C Anderson, and R Harris
J Med Genet 1985; 22: 354-360. doi:10.1136/jmg.22.5.354 [Abstract] [PDF] [Request Permissions]

The genetic control of phenformin 4-hydroxylation.
R R Shah, D A Evans, N S Oates, J R Idle, and R L Smith
J Med Genet 1985; 22: 361-366. doi:10.1136/jmg.22.5.361 [Abstract] [PDF] [Request Permissions]

A family study of hidradenitis suppurativa.
J S Fitzsimmons and P R Guilbert
J Med Genet 1985; 22: 367-373. doi:10.1136/jmg.22.5.367 [Abstract] [PDF] [Request Permissions]

Osmotic fragility test in heterozygotes for alpha and beta thalassaemia.
L Maccioni and A Cao
J Med Genet 1985; 22: 374-376. doi:10.1136/jmg.22.5.374 [Abstract] [PDF] [Request Permissions]

The first observation of Hb D Punjab beta zero thalassaemia in an English family with 22 cases of unsuspected beta zero thalassaemia minor among its members.
S Worthington and H Lehmann
J Med Genet 1985; 22: 377-381. doi:10.1136/jmg.22.5.377 [Abstract] [PDF] [Request Permissions]

Phenotypic variation in LADD syndrome.
E Thompson, M Pembrey, and J M Graham
J Med Genet 1985; 22: 382-385. doi:10.1136/jmg.22.5.382 [Abstract] [PDF] [Request Permissions]

Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.
M A Patton and K M Laurence
J Med Genet 1985; 22: 386-389. doi:10.1136/jmg.22.5.386 [Abstract] [PDF] [Request Permissions]

Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles.
T J David and R M Winter
J Med Genet 1985; 22: 390-392. doi:10.1136/jmg.22.5.390 [Abstract] [PDF] [Request Permissions]

Abstracts of the meeting of the Clinical Genetics Society. 24-25 April 1985, Birmingham.
J Med Genet 1985; 22: 393-397. doi:10.1136/jmg.22.5.393 [PDF] [Request Permissions]

Reciprocal translocation between chromosomes 8 and 9 in atypical chronic myeloid leukaemia.
D G Oscier, G J Mufti, A Gardiner, and T J Hamblin
J Med Genet 1985; 22: 398-401. doi:10.1136/jmg.22.5.398 [Abstract] [PDF] [Request Permissions]

Partial 2p deletion in a girl with a complex chromosome rearrangement involving chromosomes 2, 6, 11, and 21.
R S Young, M A Medrano, and K L Hansen
J Med Genet 1985; 22: 401-405. doi:10.1136/jmg.22.5.401 [Abstract] [PDF] [Request Permissions]

Sacrococcygeal teratoma and normal alphafetoprotein concentration in amniotic fluid.
M Szabó, P Varga, A Zalatnai, J Hidvégi, Z Tóth, and Z Papp
J Med Genet 1985; 22: 405-408. doi:10.1136/jmg.22.5.405 [Abstract] [PDF] [Request Permissions]

The Nager acrofacial dysostosis syndrome with the tetralogy of Fallot.
E Thompson, R Cadbury, and M Baraitser
J Med Genet 1985; 22: 408-410. doi:10.1136/jmg.22.5.408 [Abstract] [PDF] [Request Permissions]

Periconceptional vitamin supplementation and the prevention of neural tube defects.
P H Jongbloet
J Med Genet 1985; 22: 411-413. doi:10.1136/jmg.22.5.411 [PDF] [Request Permissions]

Attitudes of Asian families to genetic counselling.
L Mehta and I D Young
J Med Genet 1985; 22: 413. doi:10.1136/jmg.22.5.413 [PDF] [Request Permissions]

Parietal foramina in the Saethre-Chotzen syndrome.
I D Young and P G Swift
J Med Genet 1985; 22: 413-414. doi:10.1136/jmg.22.5.413-a [PDF] [Request Permissions]

Philtrum length, intercommissural distance, and ear measurements in newborn infants.
Y Sivan, P Merlob, and S H Reisner
J Med Genet 1985; 22: 414-415. doi:10.1136/jmg.22.5.414 [PDF] [Request Permissions]

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	Stanley Walker, BSc, PhD Nina M Gregson J Med Genet 1985; 22: 416. doi:10.1136/jmg.22.5.416 [PDF] [Request Permissions]

	Correction J Med Genet 1985; 22: 389. doi:10.1136/jmg.22.5.389 [PDF] [Request Permissions]

	Correspondence M J Seller and N C Nevin J Med Genet 1985; 22: 412-413. doi:10.1136/jmg.22.5.412 [PDF] [Request Permissions]

	The human Y chromosome. P Goodfellow, S Darling, and J Wolfe J Med Genet 1985; 22: 329-344. doi:10.1136/jmg.22.5.329 [Abstract] [PDF] [Request Permissions]

	Classroom teaching in genetics and birth defects: the Nottingham experience. J S Fitzsimmons J Med Genet 1985; 22: 345-349. doi:10.1136/jmg.22.5.345 [Abstract] [PDF] [Request Permissions]

	Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling. I Hausmanowa-Petrusewicz, J Zaremba, and J Borkowska J Med Genet 1985; 22: 350-353. doi:10.1136/jmg.22.5.350 [Abstract] [PDF] [Request Permissions]

	Genetics and biochemical variability of variants of 21 hydroxylase deficiency. M T Gordon, D I Conway, D C Anderson, and R Harris J Med Genet 1985; 22: 354-360. doi:10.1136/jmg.22.5.354 [Abstract] [PDF] [Request Permissions]

	The genetic control of phenformin 4-hydroxylation. R R Shah, D A Evans, N S Oates, J R Idle, and R L Smith J Med Genet 1985; 22: 361-366. doi:10.1136/jmg.22.5.361 [Abstract] [PDF] [Request Permissions]

	A family study of hidradenitis suppurativa. J S Fitzsimmons and P R Guilbert J Med Genet 1985; 22: 367-373. doi:10.1136/jmg.22.5.367 [Abstract] [PDF] [Request Permissions]

	Osmotic fragility test in heterozygotes for alpha and beta thalassaemia. L Maccioni and A Cao J Med Genet 1985; 22: 374-376. doi:10.1136/jmg.22.5.374 [Abstract] [PDF] [Request Permissions]

	The first observation of Hb D Punjab beta zero thalassaemia in an English family with 22 cases of unsuspected beta zero thalassaemia minor among its members. S Worthington and H Lehmann J Med Genet 1985; 22: 377-381. doi:10.1136/jmg.22.5.377 [Abstract] [PDF] [Request Permissions]

	Phenotypic variation in LADD syndrome. E Thompson, M Pembrey, and J M Graham J Med Genet 1985; 22: 382-385. doi:10.1136/jmg.22.5.382 [Abstract] [PDF] [Request Permissions]

	Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype. M A Patton and K M Laurence J Med Genet 1985; 22: 386-389. doi:10.1136/jmg.22.5.386 [Abstract] [PDF] [Request Permissions]

	Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles. T J David and R M Winter J Med Genet 1985; 22: 390-392. doi:10.1136/jmg.22.5.390 [Abstract] [PDF] [Request Permissions]

	Abstracts of the meeting of the Clinical Genetics Society. 24-25 April 1985, Birmingham. J Med Genet 1985; 22: 393-397. doi:10.1136/jmg.22.5.393 [PDF] [Request Permissions]

	Reciprocal translocation between chromosomes 8 and 9 in atypical chronic myeloid leukaemia. D G Oscier, G J Mufti, A Gardiner, and T J Hamblin J Med Genet 1985; 22: 398-401. doi:10.1136/jmg.22.5.398 [Abstract] [PDF] [Request Permissions]

	Partial 2p deletion in a girl with a complex chromosome rearrangement involving chromosomes 2, 6, 11, and 21. R S Young, M A Medrano, and K L Hansen J Med Genet 1985; 22: 401-405. doi:10.1136/jmg.22.5.401 [Abstract] [PDF] [Request Permissions]

	Sacrococcygeal teratoma and normal alphafetoprotein concentration in amniotic fluid. M Szabó, P Varga, A Zalatnai, J Hidvégi, Z Tóth, and Z Papp J Med Genet 1985; 22: 405-408. doi:10.1136/jmg.22.5.405 [Abstract] [PDF] [Request Permissions]

	The Nager acrofacial dysostosis syndrome with the tetralogy of Fallot. E Thompson, R Cadbury, and M Baraitser J Med Genet 1985; 22: 408-410. doi:10.1136/jmg.22.5.408 [Abstract] [PDF] [Request Permissions]

	Periconceptional vitamin supplementation and the prevention of neural tube defects. P H Jongbloet J Med Genet 1985; 22: 411-413. doi:10.1136/jmg.22.5.411 [PDF] [Request Permissions]

	Attitudes of Asian families to genetic counselling. L Mehta and I D Young J Med Genet 1985; 22: 413. doi:10.1136/jmg.22.5.413 [PDF] [Request Permissions]

	Parietal foramina in the Saethre-Chotzen syndrome. I D Young and P G Swift J Med Genet 1985; 22: 413-414. doi:10.1136/jmg.22.5.413-a [PDF] [Request Permissions]

	Philtrum length, intercommissural distance, and ear measurements in newborn infants. Y Sivan, P Merlob, and S H Reisner J Med Genet 1985; 22: 414-415. doi:10.1136/jmg.22.5.414 [PDF] [Request Permissions]