J Med Genet -- Table of Contents (26 [9])

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September 1989 (Volume 26, Number 9). [Index by author]

		Articles Editorials Correspondence Articles Book Reviews Research Article

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Articles

Abstracts of the meeting of the Clinical Genetics Society and the Clinical Molecular Genetics Society held on 30 and 31 March 1989 at the University of Southampton
J Med Genet 1989; 26: 592-601. doi:10.1136/jmg.26.9.592 [PDF] [Request Permissions]

Editorials

The clinical significance of de novo structural rearrangements and markers detected prenatally by amniocentesis
Dian Donnai
J Med Genet 1989; 26: 545. doi:10.1136/jmg.26.9.545 [PDF] [Request Permissions]

Correspondence

Reproductive behaviour and consistent patterns of abnormality in offspring of Vietnam veterans
Michael A Adena
J Med Genet 1989; 26: 602-603. doi:10.1136/jmg.26.9.602 [PDF] [Request Permissions]

Correspondence
Wayne Hall and Donald MacPhee
J Med Genet 1989; 26: 603-605. doi:10.1136/jmg.26.9.603 [PDF] [Request Permissions]

Correspondence
Charles Kerr and Barbara Field
J Med Genet 1989; 26: 606-607. doi:10.1136/jmg.26.9.606 [PDF] [Request Permissions]

Book Reviews

The Developing Human. Clinically Oriented Embryology
R F Mueller
J Med Genet 1989; 26: 608. doi:10.1136/jmg.26.9.608 [PDF] [Request Permissions]

Medical Genetics Handbook
J L Tolmie
J Med Genet 1989; 26: 608. doi:10.1136/jmg.26.9.608-a [PDF] [Request Permissions]

Research Article

Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man.
A C Chandley
J Med Genet 1989; 26: 546-552. doi:10.1136/jmg.26.9.546 [Abstract] [PDF] [Request Permissions]

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.
E Bakker, H Veenema, J T Den Dunnen, C van Broeckhoven, P M Grootscholten, E J Bonten, G J van Ommen, and P L Pearson
J Med Genet 1989; 26: 553-559. doi:10.1136/jmg.26.9.553 [Abstract] [PDF] [Request Permissions]

Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986.
A M Norman, C Rogers, J R Sibert, and P S Harper
J Med Genet 1989; 26: 560-564. doi:10.1136/jmg.26.9.560 [Abstract] [PDF] [Request Permissions]

Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.
A M Norman, M Upadhyaya, N S Thomas, K Roberts, and P S Harper
J Med Genet 1989; 26: 565-571. doi:10.1136/jmg.26.9.565 [Abstract] [PDF] [Request Permissions]

Osteoglophonic dysplasia.
P Beighton
J Med Genet 1989; 26: 572-576. doi:10.1136/jmg.26.9.572 [PDF] [Request Permissions]

Duplication of distal 17q from a maternal translocation: an additional case with some unique features.
A Caine, D M Knapton, R F Mueller, P J Congdon, and D Haigh
J Med Genet 1989; 26: 577-579. doi:10.1136/jmg.26.9.577 [Abstract] [PDF] [Request Permissions]

Moebius' syndrome with unilateral cerebellar hypoplasia.
M G Harbord, J P Finn, M A Hall-Craggs, E M Brett, and M Baraitser
J Med Genet 1989; 26: 579-582. doi:10.1136/jmg.26.9.579 [Abstract] [PDF] [Request Permissions]

3M dwarfism: a study of two further sibs.
M Feldmann, S Gilgenkrantz, S Parisot, G Zarini, and C Marchal
J Med Genet 1989; 26: 583-585. doi:10.1136/jmg.26.9.583 [Abstract] [PDF] [Request Permissions]

Choanal atresia as a feature of ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome.
J Christodoulou, P N McDougall, and L J Sheffield
J Med Genet 1989; 26: 586-589. doi:10.1136/jmg.26.9.586 [Abstract] [PDF] [Request Permissions]

Outcome of de novo balanced translocations ascertained prenatally.
D J MacGregor, S Imrie, and J L Tolmie
J Med Genet 1989; 26: 590-591. doi:10.1136/jmg.26.9.590 [PDF] [Request Permissions]

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	Abstracts of the meeting of the Clinical Genetics Society and the Clinical Molecular Genetics Society held on 30 and 31 March 1989 at the University of Southampton J Med Genet 1989; 26: 592-601. doi:10.1136/jmg.26.9.592 [PDF] [Request Permissions]

	The clinical significance of de novo structural rearrangements and markers detected prenatally by amniocentesis Dian Donnai J Med Genet 1989; 26: 545. doi:10.1136/jmg.26.9.545 [PDF] [Request Permissions]

	Reproductive behaviour and consistent patterns of abnormality in offspring of Vietnam veterans Michael A Adena J Med Genet 1989; 26: 602-603. doi:10.1136/jmg.26.9.602 [PDF] [Request Permissions]

	Correspondence Wayne Hall and Donald MacPhee J Med Genet 1989; 26: 603-605. doi:10.1136/jmg.26.9.603 [PDF] [Request Permissions]

	Correspondence Charles Kerr and Barbara Field J Med Genet 1989; 26: 606-607. doi:10.1136/jmg.26.9.606 [PDF] [Request Permissions]

	The Developing Human. Clinically Oriented Embryology R F Mueller J Med Genet 1989; 26: 608. doi:10.1136/jmg.26.9.608 [PDF] [Request Permissions]

	Medical Genetics Handbook J L Tolmie J Med Genet 1989; 26: 608. doi:10.1136/jmg.26.9.608-a [PDF] [Request Permissions]

	Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man. A C Chandley J Med Genet 1989; 26: 546-552. doi:10.1136/jmg.26.9.546 [Abstract] [PDF] [Request Permissions]

	Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations. E Bakker, H Veenema, J T Den Dunnen, C van Broeckhoven, P M Grootscholten, E J Bonten, G J van Ommen, and P L Pearson J Med Genet 1989; 26: 553-559. doi:10.1136/jmg.26.9.553 [Abstract] [PDF] [Request Permissions]

	Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986. A M Norman, C Rogers, J R Sibert, and P S Harper J Med Genet 1989; 26: 560-564. doi:10.1136/jmg.26.9.560 [Abstract] [PDF] [Request Permissions]

	Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening. A M Norman, M Upadhyaya, N S Thomas, K Roberts, and P S Harper J Med Genet 1989; 26: 565-571. doi:10.1136/jmg.26.9.565 [Abstract] [PDF] [Request Permissions]

	Osteoglophonic dysplasia. P Beighton J Med Genet 1989; 26: 572-576. doi:10.1136/jmg.26.9.572 [PDF] [Request Permissions]

	Duplication of distal 17q from a maternal translocation: an additional case with some unique features. A Caine, D M Knapton, R F Mueller, P J Congdon, and D Haigh J Med Genet 1989; 26: 577-579. doi:10.1136/jmg.26.9.577 [Abstract] [PDF] [Request Permissions]

	Moebius' syndrome with unilateral cerebellar hypoplasia. M G Harbord, J P Finn, M A Hall-Craggs, E M Brett, and M Baraitser J Med Genet 1989; 26: 579-582. doi:10.1136/jmg.26.9.579 [Abstract] [PDF] [Request Permissions]

	3M dwarfism: a study of two further sibs. M Feldmann, S Gilgenkrantz, S Parisot, G Zarini, and C Marchal J Med Genet 1989; 26: 583-585. doi:10.1136/jmg.26.9.583 [Abstract] [PDF] [Request Permissions]

	Choanal atresia as a feature of ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome. J Christodoulou, P N McDougall, and L J Sheffield J Med Genet 1989; 26: 586-589. doi:10.1136/jmg.26.9.586 [Abstract] [PDF] [Request Permissions]

	Outcome of de novo balanced translocations ascertained prenatally. D J MacGregor, S Imrie, and J L Tolmie J Med Genet 1989; 26: 590-591. doi:10.1136/jmg.26.9.590 [PDF] [Request Permissions]

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