J Med Genet -- Table of Contents (24 [10])

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October 1987 (Volume 24, Number 10). [Index by author]

		Articles Articles Book Reviews Conference Report Research Article

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Articles

Editorial
Peter S Harper
J Med Genet 1987; 24: 577. doi:10.1136/jmg.24.10.577 [PDF] [Request Permissions]

Book Reviews

Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies
J D Brook
J Med Genet 1987; 24: 645. doi:10.1136/jmg.24.10.645 [PDF] [Request Permissions]

Monitoring of Occupational Genotoxicants
J M Parry
J Med Genet 1987; 24: 645-646. doi:10.1136/jmg.24.10.645-a [PDF] [Request Permissions]

Genetic Risk
I D Young
J Med Genet 1987; 24: 646. doi:10.1136/jmg.24.10.646 [PDF] [Request Permissions]

The Harvey Lectures
Andrew P Read
J Med Genet 1987; 24: 646-647. doi:10.1136/jmg.24.10.646-a [PDF] [Request Permissions]

X Linked Mental Retardation 2
Sarah Bundey
J Med Genet 1987; 24: 647. doi:10.1136/jmg.24.10.647 [PDF] [Request Permissions]

Conference Report

Report on Conference on New Prospects in Genetic Diseases, Royal College of Physicians, 3 and 4 December 1986
J Med Genet 1987; 24: 642-643. doi:10.1136/jmg.24.10.642 [PDF] [Request Permissions]

Research Article

Disorders of haemoglobin in China.
Y T Zeng and S Z Huang
J Med Genet 1987; 24: 578-583. doi:10.1136/jmg.24.10.578 [Abstract] [PDF] [Request Permissions]

Prevalence and mode of inheritance of major genetic eye diseases in China.
D N Hu
J Med Genet 1987; 24: 584-588. doi:10.1136/jmg.24.10.584 [Abstract] [PDF] [Request Permissions]

Prevalence and genetic aspects of deaf mutism in Shanghai.
D N Hu, W Q Qiu, B T Wu, L Z Fang, F Zhou, Y P Gu, Q H Zhang, and J H Yan
J Med Genet 1987; 24: 589-592. doi:10.1136/jmg.24.10.589 [Abstract] [PDF] [Request Permissions]

The effect of hydroxyurea on the expression of the common fragile site at 3p14.
Z A Yan, X Z Li, and X T Zhou
J Med Genet 1987; 24: 593-596. doi:10.1136/jmg.24.10.593 [Abstract] [PDF] [Request Permissions]

A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?
T I Farag, S A Al-Awadi, M C Hunt, S Satyanath, M Zahran, R Usha, and R Uma
J Med Genet 1987; 24: 597-601. doi:10.1136/jmg.24.10.597 [Abstract] [PDF] [Request Permissions]

Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance.
K D MacDermot, S C Roth, C Hall, and R M Winter
J Med Genet 1987; 24: 602-608. doi:10.1136/jmg.24.10.602 [Abstract] [PDF] [Request Permissions]

Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.
S Ohdo, H Madokoro, T Sonoda, M Takei, H Yasuda, and N Mori
J Med Genet 1987; 24: 609-612. doi:10.1136/jmg.24.10.609 [Abstract] [PDF] [Request Permissions]

Hydatidiform mole: parental chromosome aberrations in partial and complete moles.
L O Vejerslev, R A Fisher, U Surti, and N Wake
J Med Genet 1987; 24: 613-615. doi:10.1136/jmg.24.10.613 [Abstract] [PDF] [Request Permissions]

Goldenhar syndrome and overlapping dysplasias, in vitro fertilisation and ovopathy.
P H Jongbloet
J Med Genet 1987; 24: 616-620. doi:10.1136/jmg.24.10.616 [Abstract] [PDF] [Request Permissions]

The Alagille syndrome (arteriohepatic dysplasia).
R F Mueller
J Med Genet 1987; 24: 621-626. doi:10.1136/jmg.24.10.621 [PDF] [Request Permissions]

Brachmann-de Lange syndrome in sibs.
K K Naguib, A S Teebi, S A Al-Awadi, and M J Marafie
J Med Genet 1987; 24: 627-629. doi:10.1136/jmg.24.10.627 [Abstract] [PDF] [Request Permissions]

A lethal presentation of de novo deletion 7q.
L E McMorrow, I R Toth, M M Gluckson, A Leff, and S R Wolman
J Med Genet 1987; 24: 629-631. doi:10.1136/jmg.24.10.629 [Abstract] [PDF] [Request Permissions]

Prenatal diagnosis of haemophilia B in the first trimester.
Y T Zeng, M L Zhang, Z R Ren, S R Chen, H L Wang, Z Y Wang, and J H Tong
J Med Genet 1987; 24: 632. doi:10.1136/jmg.24.10.632 [PDF] [Request Permissions]

An unbalanced t(X;10) mat translocation in a child with congenital abnormalities.
J Williams and P R Dear
J Med Genet 1987; 24: 633. doi:10.1136/jmg.24.10.633 [PDF] [Request Permissions]

Abstracts of the meeting of the Clinical Genetics Society. 2 and 3 April 1987, Leicester.
J Med Genet 1987; 24: 634-641. doi:10.1136/jmg.24.10.634 [PDF] [Request Permissions]

IVF and Goldenhar syndrome.
J Yovich, M Mulcahy, and P Matson
J Med Genet 1987; 24: 644. doi:10.1136/jmg.24.10.644 [PDF] [Request Permissions]

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	Editorial Peter S Harper J Med Genet 1987; 24: 577. doi:10.1136/jmg.24.10.577 [PDF] [Request Permissions]

	Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies J D Brook J Med Genet 1987; 24: 645. doi:10.1136/jmg.24.10.645 [PDF] [Request Permissions]

	Monitoring of Occupational Genotoxicants J M Parry J Med Genet 1987; 24: 645-646. doi:10.1136/jmg.24.10.645-a [PDF] [Request Permissions]

	Genetic Risk I D Young J Med Genet 1987; 24: 646. doi:10.1136/jmg.24.10.646 [PDF] [Request Permissions]

	The Harvey Lectures Andrew P Read J Med Genet 1987; 24: 646-647. doi:10.1136/jmg.24.10.646-a [PDF] [Request Permissions]

	X Linked Mental Retardation 2 Sarah Bundey J Med Genet 1987; 24: 647. doi:10.1136/jmg.24.10.647 [PDF] [Request Permissions]

	Report on Conference on New Prospects in Genetic Diseases, Royal College of Physicians, 3 and 4 December 1986 J Med Genet 1987; 24: 642-643. doi:10.1136/jmg.24.10.642 [PDF] [Request Permissions]

	Disorders of haemoglobin in China. Y T Zeng and S Z Huang J Med Genet 1987; 24: 578-583. doi:10.1136/jmg.24.10.578 [Abstract] [PDF] [Request Permissions]

	Prevalence and mode of inheritance of major genetic eye diseases in China. D N Hu J Med Genet 1987; 24: 584-588. doi:10.1136/jmg.24.10.584 [Abstract] [PDF] [Request Permissions]

	Prevalence and genetic aspects of deaf mutism in Shanghai. D N Hu, W Q Qiu, B T Wu, L Z Fang, F Zhou, Y P Gu, Q H Zhang, and J H Yan J Med Genet 1987; 24: 589-592. doi:10.1136/jmg.24.10.589 [Abstract] [PDF] [Request Permissions]

	The effect of hydroxyurea on the expression of the common fragile site at 3p14. Z A Yan, X Z Li, and X T Zhou J Med Genet 1987; 24: 593-596. doi:10.1136/jmg.24.10.593 [Abstract] [PDF] [Request Permissions]

	A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance? T I Farag, S A Al-Awadi, M C Hunt, S Satyanath, M Zahran, R Usha, and R Uma J Med Genet 1987; 24: 597-601. doi:10.1136/jmg.24.10.597 [Abstract] [PDF] [Request Permissions]

	Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance. K D MacDermot, S C Roth, C Hall, and R M Winter J Med Genet 1987; 24: 602-608. doi:10.1136/jmg.24.10.602 [Abstract] [PDF] [Request Permissions]

	Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation. S Ohdo, H Madokoro, T Sonoda, M Takei, H Yasuda, and N Mori J Med Genet 1987; 24: 609-612. doi:10.1136/jmg.24.10.609 [Abstract] [PDF] [Request Permissions]

	Hydatidiform mole: parental chromosome aberrations in partial and complete moles. L O Vejerslev, R A Fisher, U Surti, and N Wake J Med Genet 1987; 24: 613-615. doi:10.1136/jmg.24.10.613 [Abstract] [PDF] [Request Permissions]

	Goldenhar syndrome and overlapping dysplasias, in vitro fertilisation and ovopathy. P H Jongbloet J Med Genet 1987; 24: 616-620. doi:10.1136/jmg.24.10.616 [Abstract] [PDF] [Request Permissions]

	The Alagille syndrome (arteriohepatic dysplasia). R F Mueller J Med Genet 1987; 24: 621-626. doi:10.1136/jmg.24.10.621 [PDF] [Request Permissions]

	Brachmann-de Lange syndrome in sibs. K K Naguib, A S Teebi, S A Al-Awadi, and M J Marafie J Med Genet 1987; 24: 627-629. doi:10.1136/jmg.24.10.627 [Abstract] [PDF] [Request Permissions]

	A lethal presentation of de novo deletion 7q. L E McMorrow, I R Toth, M M Gluckson, A Leff, and S R Wolman J Med Genet 1987; 24: 629-631. doi:10.1136/jmg.24.10.629 [Abstract] [PDF] [Request Permissions]

	Prenatal diagnosis of haemophilia B in the first trimester. Y T Zeng, M L Zhang, Z R Ren, S R Chen, H L Wang, Z Y Wang, and J H Tong J Med Genet 1987; 24: 632. doi:10.1136/jmg.24.10.632 [PDF] [Request Permissions]

	An unbalanced t(X;10) mat translocation in a child with congenital abnormalities. J Williams and P R Dear J Med Genet 1987; 24: 633. doi:10.1136/jmg.24.10.633 [PDF] [Request Permissions]

	Abstracts of the meeting of the Clinical Genetics Society. 2 and 3 April 1987, Leicester. J Med Genet 1987; 24: 634-641. doi:10.1136/jmg.24.10.634 [PDF] [Request Permissions]

	IVF and Goldenhar syndrome. J Yovich, M Mulcahy, and P Matson J Med Genet 1987; 24: 644. doi:10.1136/jmg.24.10.644 [PDF] [Request Permissions]