Volume 9, Issue 1 supplement

Journal of Inherited Metabolic Disease is now archived and no longer receiving submissions with this publisher. All articles published in the journal during its time with Springer will remain fully searchable through our websites.

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March 1986

19 articles in this issue

Preface
G. M. Addison
R. A Harkness
R. J. Pollitt
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 1 - 2
Introduction to recombinant DNA
J. Scott
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 3 - 16
Human biochemical genetics of enzyme proteins in the new age of molecular genetics
D. M. Swallow
D. A. Hopkinson
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 17 - 31
Direct DNA analysis in family studies
S. Malcolm
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 32 - 37
Applications and limitations of direct DNA analysis in genetic prediction
M. E. Pembrey
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 38 - 48
DNA analysis for ornithine transcarbamylase deficiency
R. Rozen
J. E. Fox
L. E. Rosenberg
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 49 - 57
Molecular genetics of PKU
F. Güttler
S. L. C. Woo
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 58 - 68
Human DNA repair defects
C. F. Arlett
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 69 - 84
Molecular basis of α₁-antitrypsin deficiency and its potential therapy by gene transfer
F. D. Ledley
S. L. C. Woo
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 85 - 91
Direct alteration of a gene in the human genome
O. Smithies
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 92 - 97
Diabetes mellitus, atherosclerosis, and the 5′ flanking polymorphism of the human insulin gene
T. Mandrup-Poulsen
D. Owerbach
A. Tybjærg Hansen
The 23rd Annual Symposium Of The SSIEM: Liverpool 1985 Pages: 98 - 110
Introduction
G. M. Addison
Workshop On Screening For Congenital Adrenal Hyperplasia (Steroid 21-Hydroxylase Deficiency) Pages: 111 - 114
Clinical aspects of congenital adrenal hyperplasia: Early diagnosis and prognosis
I. A. Hughes
Workshop On Screening For Congenital Adrenal Hyperplasia (Steroid 21-Hydroxylase Deficiency) Pages: 115 - 123
Biochemical aspects of congenital adrenal hyperplasia
J. Honour
Workshop On Screening For Congenital Adrenal Hyperplasia (Steroid 21-Hydroxylase Deficiency) Pages: 124 - 134
Review of CAH screening programmes and the Scottish experience
A. M. Wallace
Large Scale Pilot Studies Pages: 135 - 141
Neonatal screening programme for congenital adrenal hyperplasia in a homogenous Caucasian population
E. Cacciari
A. Balsamo
C. I. Cordaro
Large Scale Pilot Studies Pages: 142 - 146
Neonatal screening for congenital adrenal hyperplasia: a pilot study in France
J. L. Dhondt
C. Dorche
C. Courte
Large Scale Pilot Studies Pages: 147 - 151
Congenital adrenal hyperplasia in Birmingham: a retrospective analysis (1958–1985)
N. K. Virdi
A. Green
Existing Clinical Diagnoses Pages: 152 - 155
Prevalence of adrenal 21-hydroxylase deficiency in neonates born in the West Midlands: a retrospective study
B. T. Rudd
Existing Clinical Diagnoses Pages: 155 - 156

Volume 9, Issue 1 supplement

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