J Med Genet -- Table of Contents (14 [2])

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April 1977 (Volume 14, Number 2). [Index by author]

		Book Reviews Research Article

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Book Reviews

Racial Variation in Man. (Institute of Biology Symposium No. 22.)
C. E. Blank
J Med Genet 1977; 14: 154. doi:10.1136/jmg.14.2.154 [PDF] [Request Permissions]

Human Multiple Reproduction
M. G. Bulmer
J Med Genet 1977; 14: 154. doi:10.1136/jmg.14.2.154-a [PDF] [Request Permissions]

Diseases of the Fundus Oculi
Barrie Jay
J Med Genet 1977; 14: 155. doi:10.1136/jmg.14.2.155 [PDF] [Request Permissions]

Control of Gene Expression
D. J. Weatherall
J Med Genet 1977; 14: 155-156. doi:10.1136/jmg.14.2.155-a [PDF] [Request Permissions]

Genetics and the Law
Alan E. H. Emery
J Med Genet 1977; 14: 156. doi:10.1136/jmg.14.2.156 [PDF] [Request Permissions]

Research Article

Occurrence of childhood cancers among sibs and estimation of familial risks.
G J Draper, M M Heaf, and L M Kinnier Wilson
J Med Genet 1977; 14: 81-90. doi:10.1136/jmg.14.2.81 [Abstract] [PDF] [Request Permissions]

Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles.
M W Spence, A L Goldbloom, J K Burgess, D D'entremont, B A Ripley, and K L Weldon
J Med Genet 1977; 14: 91-99. doi:10.1136/jmg.14.2.91 [Abstract] [PDF] [Request Permissions]

Rapid prenatal diagnosis of the Lesch-Nyhan syndrome.
D Halley and M J Heukels-Dully
J Med Genet 1977; 14: 100-102. doi:10.1136/jmg.14.2.100 [Abstract] [PDF] [Request Permissions]

Genetic heterogeneity within the chondroitinsulphaturias.
B S Danes, B K Rottell, L Eviatar, and J Stolzenberg
J Med Genet 1977; 14: 103-107. doi:10.1136/jmg.14.2.103 [Abstract] [PDF] [Request Permissions]

Problem of sex ratio in cases of type I syndactyly.
C M Woolf and D L Cone
J Med Genet 1977; 14: 108-113. doi:10.1136/jmg.14.2.108 [Abstract] [PDF] [Request Permissions]

Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.
H J Kim, L Y Hsu, L C Goldsmith, L Strauss, and K Hirschhorn
J Med Genet 1977; 14: 114-119. doi:10.1136/jmg.14.2.114 [Abstract] [PDF] [Request Permissions]

Prenatal diagnosis and gonadal findings in X/XXX mosaicism.
G Kohn, M M Cohen, Y Beyth, and A Ornoy
J Med Genet 1977; 14: 120-123. doi:10.1136/jmg.14.2.120 [Abstract] [PDF] [Request Permissions]

Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.
J Simpson and H Zellweger
J Med Genet 1977; 14: 124-127. doi:10.1136/jmg.14.2.124 [Abstract] [PDF] [Request Permissions]

Gonadal dysgenesis with Graves's disease.
W H Brooks, J C Meek, and R N Schimke
J Med Genet 1977; 14: 128-129. doi:10.1136/jmg.14.2.128 [Abstract] [PDF] [Request Permissions]

Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating.
D N Greig
J Med Genet 1977; 14: 130-132. doi:10.1136/jmg.14.2.130 [Abstract] [PDF] [Request Permissions]

GM1 gangliosidosis type 1 in twins.
C M Ginsburg and C G Long
J Med Genet 1977; 14: 132-134. doi:10.1136/jmg.14.2.132 [Abstract] [PDF] [Request Permissions]

Reproductive ability of an adult female with Silver-Russell syndrome.
H K Abramowicz and H M Nitowsky
J Med Genet 1977; 14: 134-136. doi:10.1136/jmg.14.2.134 [Abstract] [PDF] [Request Permissions]

Autosomal recessive hydrotic ectodermal dysplasia.
K Fried
J Med Genet 1977; 14: 137-139. doi:10.1136/jmg.14.2.137 [Abstract] [PDF] [Request Permissions]

Recessive form of Freeman-Sheldon's syndrome or 'whistling face'.
A F Alves and E S Azevedo
J Med Genet 1977; 14: 139-141. doi:10.1136/jmg.14.2.139 [Abstract] [PDF] [Request Permissions]

Two reciprocal translocations associated with microcephaly and retardation.
E F Bell and D Warburton
J Med Genet 1977; 14: 141-142. doi:10.1136/jmg.14.2.141 [Abstract] [PDF] [Request Permissions]

De novo balanced reciprocal translocation 46,XY,t(6;8)(q13;q22).
K Fried, M Rosenblatt, and G Mundel
J Med Genet 1977; 14: 142-144. doi:10.1136/jmg.14.2.142 [Abstract] [PDF] [Request Permissions]

A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).
B G Kousseff, L Y Hsu, S Paciuc, and K Hirschhorn
J Med Genet 1977; 14: 144-147. doi:10.1136/jmg.14.2.144 [Abstract] [PDF] [Request Permissions]

Down's syndrome and deletion of short arms of a G chromosome.
G H Ballantyne, M I Parslow, A M Veale, and D H Pullon
J Med Genet 1977; 14: 147-150. doi:10.1136/jmg.14.2.147 [Abstract] [PDF] [Request Permissions]

Sex chromatin and the biological effects of triploidy.
U Mittwoch
J Med Genet 1977; 14: 151. doi:10.1136/jmg.14.2.151 [PDF] [Request Permissions]

Extra chromosome in Kallmann's syndrome.
E Kemmann
J Med Genet 1977; 14: 151-152. doi:10.1136/jmg.14.2.151-a [PDF] [Request Permissions]

'Mirror image' chromosome No. 21.
J Harvey, S Wiener, and R Birner
J Med Genet 1977; 14: 152-153. doi:10.1136/jmg.14.2.152 [PDF] [Request Permissions]

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	Racial Variation in Man. (Institute of Biology Symposium No. 22.) C. E. Blank J Med Genet 1977; 14: 154. doi:10.1136/jmg.14.2.154 [PDF] [Request Permissions]

	Human Multiple Reproduction M. G. Bulmer J Med Genet 1977; 14: 154. doi:10.1136/jmg.14.2.154-a [PDF] [Request Permissions]

	Diseases of the Fundus Oculi Barrie Jay J Med Genet 1977; 14: 155. doi:10.1136/jmg.14.2.155 [PDF] [Request Permissions]

	Control of Gene Expression D. J. Weatherall J Med Genet 1977; 14: 155-156. doi:10.1136/jmg.14.2.155-a [PDF] [Request Permissions]

	Genetics and the Law Alan E. H. Emery J Med Genet 1977; 14: 156. doi:10.1136/jmg.14.2.156 [PDF] [Request Permissions]

	Occurrence of childhood cancers among sibs and estimation of familial risks. G J Draper, M M Heaf, and L M Kinnier Wilson J Med Genet 1977; 14: 81-90. doi:10.1136/jmg.14.2.81 [Abstract] [PDF] [Request Permissions]

	Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles. M W Spence, A L Goldbloom, J K Burgess, D D'entremont, B A Ripley, and K L Weldon J Med Genet 1977; 14: 91-99. doi:10.1136/jmg.14.2.91 [Abstract] [PDF] [Request Permissions]

	Rapid prenatal diagnosis of the Lesch-Nyhan syndrome. D Halley and M J Heukels-Dully J Med Genet 1977; 14: 100-102. doi:10.1136/jmg.14.2.100 [Abstract] [PDF] [Request Permissions]

	Genetic heterogeneity within the chondroitinsulphaturias. B S Danes, B K Rottell, L Eviatar, and J Stolzenberg J Med Genet 1977; 14: 103-107. doi:10.1136/jmg.14.2.103 [Abstract] [PDF] [Request Permissions]

	Problem of sex ratio in cases of type I syndactyly. C M Woolf and D L Cone J Med Genet 1977; 14: 108-113. doi:10.1136/jmg.14.2.108 [Abstract] [PDF] [Request Permissions]

	Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. H J Kim, L Y Hsu, L C Goldsmith, L Strauss, and K Hirschhorn J Med Genet 1977; 14: 114-119. doi:10.1136/jmg.14.2.114 [Abstract] [PDF] [Request Permissions]

	Prenatal diagnosis and gonadal findings in X/XXX mosaicism. G Kohn, M M Cohen, Y Beyth, and A Ornoy J Med Genet 1977; 14: 120-123. doi:10.1136/jmg.14.2.120 [Abstract] [PDF] [Request Permissions]

	Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature. J Simpson and H Zellweger J Med Genet 1977; 14: 124-127. doi:10.1136/jmg.14.2.124 [Abstract] [PDF] [Request Permissions]

	Gonadal dysgenesis with Graves's disease. W H Brooks, J C Meek, and R N Schimke J Med Genet 1977; 14: 128-129. doi:10.1136/jmg.14.2.128 [Abstract] [PDF] [Request Permissions]

	Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating. D N Greig J Med Genet 1977; 14: 130-132. doi:10.1136/jmg.14.2.130 [Abstract] [PDF] [Request Permissions]

	GM1 gangliosidosis type 1 in twins. C M Ginsburg and C G Long J Med Genet 1977; 14: 132-134. doi:10.1136/jmg.14.2.132 [Abstract] [PDF] [Request Permissions]

	Reproductive ability of an adult female with Silver-Russell syndrome. H K Abramowicz and H M Nitowsky J Med Genet 1977; 14: 134-136. doi:10.1136/jmg.14.2.134 [Abstract] [PDF] [Request Permissions]

	Autosomal recessive hydrotic ectodermal dysplasia. K Fried J Med Genet 1977; 14: 137-139. doi:10.1136/jmg.14.2.137 [Abstract] [PDF] [Request Permissions]

	Recessive form of Freeman-Sheldon's syndrome or 'whistling face'. A F Alves and E S Azevedo J Med Genet 1977; 14: 139-141. doi:10.1136/jmg.14.2.139 [Abstract] [PDF] [Request Permissions]

	Two reciprocal translocations associated with microcephaly and retardation. E F Bell and D Warburton J Med Genet 1977; 14: 141-142. doi:10.1136/jmg.14.2.141 [Abstract] [PDF] [Request Permissions]

	De novo balanced reciprocal translocation 46,XY,t(6;8)(q13;q22). K Fried, M Rosenblatt, and G Mundel J Med Genet 1977; 14: 142-144. doi:10.1136/jmg.14.2.142 [Abstract] [PDF] [Request Permissions]

	A partial long arm deletion of chromosome 7:46,XY,del(7)(q32). B G Kousseff, L Y Hsu, S Paciuc, and K Hirschhorn J Med Genet 1977; 14: 144-147. doi:10.1136/jmg.14.2.144 [Abstract] [PDF] [Request Permissions]

	Down's syndrome and deletion of short arms of a G chromosome. G H Ballantyne, M I Parslow, A M Veale, and D H Pullon J Med Genet 1977; 14: 147-150. doi:10.1136/jmg.14.2.147 [Abstract] [PDF] [Request Permissions]

	Sex chromatin and the biological effects of triploidy. U Mittwoch J Med Genet 1977; 14: 151. doi:10.1136/jmg.14.2.151 [PDF] [Request Permissions]

	Extra chromosome in Kallmann's syndrome. E Kemmann J Med Genet 1977; 14: 151-152. doi:10.1136/jmg.14.2.151-a [PDF] [Request Permissions]

	'Mirror image' chromosome No. 21. J Harvey, S Wiener, and R Birner J Med Genet 1977; 14: 152-153. doi:10.1136/jmg.14.2.152 [PDF] [Request Permissions]