de Jong G - Search Results

1

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.

Bardien S, Human H, Harris T, Hefke G, Veikondis R, Schaaf HS, van der Merwe L, Greinwald JH, Fagan J, de Jong G. Bardien S, et al. Among authors: de jong g. BMC Med Genet. 2009 Jan 13;10:2. doi: 10.1186/1471-2350-10-2. BMC Med Genet. 2009. PMID: 19144107 Free PMC article.

2

A South African family with the mitochondrial A1555G mutation on haplogroup L0d.

Human H, Lombard D, de Jong G, Bardien S. Human H, et al. Among authors: de jong g. Biochem Biophys Res Commun. 2009 May 1;382(2):390-4. doi: 10.1016/j.bbrc.2009.03.032. Epub 2009 Mar 12. Biochem Biophys Res Commun. 2009. PMID: 19285484

3

Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides.

Human H, Hagen CM, de Jong G, Harris T, Lombard D, Christiansen M, Bardien S. Human H, et al. Among authors: de jong g. Biochem Biophys Res Commun. 2010 Mar 19;393(4):751-6. doi: 10.1016/j.bbrc.2010.02.075. Epub 2010 Feb 18. Biochem Biophys Res Commun. 2010. PMID: 20171168

4

Aminoglycoside-induced hearing loss in HIV-positive and HIV-negative multidrug-resistant tuberculosis patients.

Harris T, Bardien S, Schaaf HS, Petersen L, De Jong G, Fagan JJ. Harris T, et al. Among authors: de jong g. S Afr Med J. 2012 May 8;102(6 Pt 2):363-6. doi: 10.7196/samj.4964. S Afr Med J. 2012. PMID: 22668907

5

Aminoglycoside-induced hearing loss: South Africans at risk.

Bardien S, de Jong G, Schaaf HS, Harris T, Fagan J, Petersen L. Bardien S, et al. Among authors: de jong g. S Afr Med J. 2009 Jun;99(6):440-1. S Afr Med J. 2009. PMID: 19736844 No abstract available.

6

A study of meningiomas in South Africa: investigating a correlation between clinical presentation, histopathology and genetic markers.

Vivier J, Bardien S, Van der Merwe L, Brusnicky J, Zaharie D, Keyser R, Hewlett R, de Jong G, Hartzenberg B. Vivier J, et al. Among authors: de jong g. Br J Neurosurg. 2009 Feb;23(1):63-70. doi: 10.1080/02688690802593064. Br J Neurosurg. 2009. PMID: 19234911

7

Chromosome 22q11 in a Xhosa schizophrenia population.

Koen L, Niehaus DJ, Wright G, Warnich L, De Jong G, Emsley RA, Mall S. Koen L, et al. Among authors: de jong g. S Afr Med J. 2012 Feb 23;102(3 Pt 1):165-6. doi: 10.7196/samj.5326. S Afr Med J. 2012. PMID: 22380913 Free article.

8

Morphological features in a Xhosa schizophrenia population.

Koen L, Niehaus DJ, De Jong G, Muller JE, Jordaan E. Koen L, et al. Among authors: de jong g. BMC Psychiatry. 2006 Oct 27;6:47. doi: 10.1186/1471-244X-6-47. BMC Psychiatry. 2006. PMID: 17069645 Free PMC article.

9

Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type I.

Mathew CG, Thorpe K, Easton DF, Chin KS, Jadayel D, Ponder M, Moore G, Wallis CE, Slater CP, De Jong G, et al. Mathew CG, et al. Among authors: de jong g. Am J Hum Genet. 1989 Jan;44(1):38-40. Am J Hum Genet. 1989. PMID: 2491780 Free PMC article.

10

Oculocerebral syndrome with hypopigmentation (Cross syndrome): the mixed pattern of hair pigmentation as an important diagnostic sign.

De Jong G, Fryns JP. De Jong G, et al. Genet Couns. 1991;2(3):151-5. Genet Couns. 1991. PMID: 1801851

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