Osteoglophonic dysplasia: A 'common' mutation in a rare disease

A. J. Sow, Roszalina Ramli, Zarina Abdul Latiff, S. Ichikawa, A. K. Gray, Rifqah Nordin, Mohd Nazimi Abd Jabar, S. H A Primuharsa Putra, C. H. Siar, M. J. Econs

Research output: Contribution to journalArticle

4 Citations (Scopus)
Original languageEnglish
Pages (from-to)197-198
Number of pages2
JournalClinical Genetics
Volume78
Issue number2
DOIs
Publication statusPublished - Aug 2010

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DNA Mutational Analysis
Molecular Sequence Data
Receptor, Fibroblast Growth Factor, Type 1
Dwarfism
Preschool Children
Heterozygote
Rare Diseases
Exons
Mutation
Osteoglophonic dwarfism

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Osteoglophonic dysplasia : A 'common' mutation in a rare disease. / Sow, A. J.; Ramli, Roszalina; Abdul Latiff, Zarina; Ichikawa, S.; Gray, A. K.; Nordin, Rifqah; Abd Jabar, Mohd Nazimi; Primuharsa Putra, S. H A; Siar, C. H.; Econs, M. J.

In: Clinical Genetics, Vol. 78, No. 2, 08.2010, p. 197-198.

Research output: Contribution to journalArticle

Sow, A. J. ; Ramli, Roszalina ; Abdul Latiff, Zarina ; Ichikawa, S. ; Gray, A. K. ; Nordin, Rifqah ; Abd Jabar, Mohd Nazimi ; Primuharsa Putra, S. H A ; Siar, C. H. ; Econs, M. J. / Osteoglophonic dysplasia : A 'common' mutation in a rare disease. In: Clinical Genetics. 2010 ; Vol. 78, No. 2. pp. 197-198.
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