FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Robea Ballo

Research Profile

Geographic Areas

Concepts & Ideas

Living Beings

African Continental Ancestry Group

Disorders

Physiology

Procedures

Phenomena

Polymorphism, Single-Stranded Conformational

Anatomy

X Chromosome

Chemicals & Drugs

Co-author Network

Publications

TOP 3
Robea Ballo; L J Greenberg; Susan H Kidson
A new class of stem cells in South Africa: iPS cells.
J M Heckmann; H Uwimpuhwe; Robea Ballo; M Kaur; Vladimir Bajic; Sharon Prince
A functional SNP in the regulatory region of the decay-accelerating factor gene associates with extraocular muscle pareses in myasthenia gravis.
Collet Dandara; Robea Ballo; M Iqbal Parker
CYP3A5 genotypes and risk of oesophageal cancer in two South African populations.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Robea Ballo (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Robea Ballo; L J Greenberg; Susan H Kidson
A new class of stem cells in South Africa: iPS cells.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2013;103(1):16-7.
2010: J M Heckmann; H Uwimpuhwe; Robea Ballo; M Kaur; Vladimir Bajic; Sharon Prince
A functional SNP in the regulatory region of the decay-accelerating factor gene associates with extraocular muscle pareses in myasthenia gravis.
Genes and immunity 2010;11(1):1-10.
2005: Collet Dandara; Robea Ballo; M Iqbal Parker
CYP3A5 genotypes and risk of oesophageal cancer in two South African populations.
Cancer letters 2005;225(2):275-82.
2003: Robea Ballo; Dong-Ping Li; M Iqbal Parker
Genotyping of alcohol dehydrogenase type 2 and 3 using a two-buffer polyacrylamide gel electrophoresis system.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2003;41(3):298-301.
1998: Robea Ballo; Peter Beighton; Rajkumar Ramesar
Stickler-like syndrome due to a dominant negative mutation in the COL2A1 gene.
American journal of medical genetics 1998;80(1):6-11.
1997: Robea Ballo; Michael D Briggs; Daniel H Cohn; RG Knowlton; Peter Beighton; Rajkumar Ramesar
Multiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African family.
American journal of medical genetics 1997;68(4):396-400.
1996: Robea Ballo; Denis L Viljoen; M Machado; Douglas R Keene; W Horton; V Fredlund; M Jacobs; R Martell; Peter Beighton; Rajkumar Ramesar
Mseleni joint disease--a molecular genetic approach to defining the aetiology.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1996;86(8):956-8.
1994: Robea Ballo; Denis L Viljoen; Peter Beighton
Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1994;84(8 Pt 1):494-7.
1991: Robea Ballo; H W Hitzeroth; Peter Beighton
Duchenne muscular dystrophy--a molecular service.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1991;79(4):209-12.
1989: J Goldblatt; Robea Ballo; B Sachs; A Moosa
X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype.
Clinical genetics 1989;35(2):116-20.
1988: C Wallis; Robea Ballo; G Wallis; Peter Beighton; J Goldblatt
X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.
Genomics 1988;3(4):299-301.
1987: J Goldblatt; Robea Ballo; G Wallis; J Shapera; Peter Beighton
Duchenne muscular dystrophy in South Africa. Prevention by molecular techniques.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1987;72(12):835-7.