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

A. J. Sow, R. Ramli, Z. A. Latiff, S. Ichikawa, A. K. Gray, R. Nordin, M. N. Abd Jabar, S. H.A. Primuharsa Putra, C. H. Siar, M. J. Econs

Research output: Contribution to journalLetter

5 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)197-198
Number of pages2
JournalClinical Genetics
Volume78
Issue number2
DOIs
StatePublished - Aug 1 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
  • Genetics(clinical)

Cite this

Sow, A. J., Ramli, R., Latiff, Z. A., Ichikawa, S., Gray, A. K., Nordin, R., ... Econs, M. J. (2010). Osteoglophonic dysplasia: A 'common' mutation in a rare disease. Clinical Genetics, 78(2), 197-198. https://doi.org/10.1111/j.1399-0004.2010.01382.x

Osteoglophonic dysplasia : A 'common' mutation in a rare disease. / Sow, A. J.; Ramli, R.; Latiff, Z. A.; Ichikawa, S.; Gray, A. K.; Nordin, R.; Abd Jabar, M. N.; Primuharsa Putra, S. H.A.; Siar, C. H.; Econs, M. J.

In: Clinical Genetics, Vol. 78, No. 2, 01.08.2010, p. 197-198.

Research output: Contribution to journalLetter

Sow, AJ, Ramli, R, Latiff, ZA, Ichikawa, S, Gray, AK, Nordin, R, Abd Jabar, MN, Primuharsa Putra, SHA, Siar, CH & Econs, MJ 2010, 'Osteoglophonic dysplasia: A 'common' mutation in a rare disease', Clinical Genetics, vol. 78, no. 2, pp. 197-198. https://doi.org/10.1111/j.1399-0004.2010.01382.x
Sow AJ, Ramli R, Latiff ZA, Ichikawa S, Gray AK, Nordin R et al. Osteoglophonic dysplasia: A 'common' mutation in a rare disease. Clinical Genetics. 2010 Aug 1;78(2):197-198. https://doi.org/10.1111/j.1399-0004.2010.01382.x
Sow, A. J. ; Ramli, R. ; Latiff, Z. A. ; Ichikawa, S. ; Gray, A. K. ; Nordin, R. ; Abd Jabar, M. N. ; 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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