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Human Heredity|March 24, 2012
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing dataJennifer L Asimit, Aaron G Day-Williams, Andrew P Morris, et al.
Genomics|September 1, 1993
Sequence of the human iduronate 2-sulfatase (IDS) geneP J Wilson, C A Meaney, J J Hopwood, et al.
American Journal of Medical Genetics|January 15, 1994
Mutation analysis of 28 Gaucher disease patients: the Australasian experienceB D Lewis, P V Nelson, E F Robertson, et al.
Child Abuse & Neglect|December 29, 2000
Home visiting intervention for vulnerable families with newborns: follow-up results of a randomized controlled trialJ A Fraser, K L Armstrong, J P Morris, et al.
Clinical Epidemiology|July 30, 2021
Current Practices in Missing Data Handling for Interrupted Time Series Studies Performed on Individual-Level Data: A Scoping Review in Health ResearchJuan Carlos Bazo-Alvarez, Tim P Morris, James R Carpenter, et al.
The Journal of Bone and Joint Surgery. British Volume|August 1, 1984
The management of equinus deformity in Duchenne muscular dystrophyE A Williams, L Read, A Ellis, et al.
Developmental Neuroscience|January 1, 1993
Studies on metabolic regulation using NMR spectroscopyH Bachelard, R Badar-Goffer, O Ben-Yoseph, et al.
Human Mutation|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, J Zlotogora, A Harris, et al.
Archives of Disease in Childhood|June 23, 2005
A new formula for blood transfusion volume in the critically illK P Morris, N Naqvi, P Davies, et al.
Biochimica Et Biophysica Acta|April 15, 1976
RNA polymerases from a rat hepatoma. Partial purification and comparison of properties with corresponding liver enzymesK M Rose, P A Ruch, H P Morris, et al.
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