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- Publications
- Influence
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III.
- H. J. Luedecke, J. Schaper, +37 authors B. Horsthemke
- Biology, Medicine
- American journal of human genetics
- 2001
Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;… Expand
Spending for Development: making the most of Indonesia's new opportunities - Indonesia Public Expenditure Review - By The World Bank
- R. Mcleod
- Economics
- 1 November 2009
Soeharto’s Indonesia: A Better Class of Corruption
- R. Mcleod
- Political Science
- 2000
"TTndonesia has a reputation as one of the most corrupt countries in the world I (Transparency International, 1999). Unlike many others that are regarded as highly corrupt, however, this was not… Expand
A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots.
- D. Whiteside, R. Mcleod, +4 authors S. Andrew
- Medicine
- Cancer research
- 15 January 2002
Individuals with a germ-line mutation in one of the DNA mismatch repair (MMR) genes are at significant risk for colorectal cancer and other tumors. Three families have previously been reported with… Expand
The struggle to regain effective government under democracy in Indonesia
- R. Mcleod
- Economics
- 1 December 2005
With Soeharto's demise, Indonesia gained democracy but lost effective government. A return to sustained, rapid economic growth will require an overhaul of Indonesia's bureaucracy and judiciary which,… Expand
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.
- Steven C. Greenway, R. Mcleod, +9 authors B. Gerull
- Medicine
- The Canadian journal of cardiology
- 1 February 2014
BACKGROUND
The genetics of congenital heart disease (CHD) remain incompletely understood. Exome sequencing has been successfully used to identify disease-causing mutations in familial disorders in… Expand
Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH
- C. Tyson, Y. Qiao, +20 authors E. Rajcan-Separovic
- Biology, Medicine
- Molecular Cytogenetics
- 11 November 2008
BackgroundJacobsen syndrome is a rare contiguous gene disorder that results from a terminal deletion of the long arm of chromosome 11. It is typically characterized by intellectual disability, a… Expand
East Asia in crisis : from being a miracle to needing one?
- R. Mcleod, R. Garnaut
- History
- 1998
Part I. Overview 1. East Asia in Crisis Ross Garnaut and Ross McLeod Part II. Case Studies: The Troubled Economies 2. Indonesia Ross McLeod 3. Thailand Peter G. Warr 4. Korea Heather Smith 5.… Expand
Fiscal Transfers to Regional Governments in Indonesia
This paper examines the design of the fiscal 'equalisation', or 'balancing', arrangements introduced in Indonesia in 2001, when many functions were devolved from the central to regional governments.… Expand
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