G. de Jong

发表

Aminoglycoside-induced hearing loss: South Africans at risk.

S. Bardien, H. S. Schaaf, G. de Jong, 2009, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Prenatal diagnosis of congenital leukemia in a fetus at 25 weeks' gestation with Down syndrome: case report and review of the literature

G. de Jong, E. Mansvelt, M. Robertson, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

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

S. Bardien, J. Fagan, H. S. Schaaf, 2012, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Ring chromosome 15 in a patient with features of Fryns' syndrome.

G. de Jong, A. Retief, R. Rossouw, 1989, Journal of medical genetics.

RSH (Smith-Lemli-Opitz) syndrome: "severe" phenotype with ectrodactyly.

L. Muller, P. Kirby, G. de Jong, 1998, American journal of medical genetics.

The antenatal ultrasonographic detection of the Holt-Oram syndrome.

G. de Jong, L. Muller, K. M. van Heerden, 1985, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.

R. Hennekam, J. Allanson, D. Lacombe, 2002, American journal of medical genetics.

Perinatal death in two sibs with infantile cortical hyperostosis (Caffey disease).

G. de Jong, L. Muller, 1995, American journal of medical genetics.

Proteus syndrome in southern Africa: natural history and clinical manifestations in six individuals.

P. Beighton, D. Viljoen, G. de Jong, 1987, American journal of medical genetics.

Prenatal ultrasonographic features of the Pena-Shokeir I syndrome and the trisomy 18 syndrome.

G. de Jong, L. Muller, 1986, American journal of medical genetics.

Defects of blastogenesis: counseling dilemmas in two families.

P. Kirby, G. de Jong, 2000, American journal of medical genetics.

A case of the Neu-Laxova syndrome: prenatal ultrasonographic monitoring in the third trimester and the histopathological findings.

P. Kirby, G. de Jong, M. Greeff, 1987, American journal of medical genetics.

Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

G. de Jong, J. Brusnicky, A. Retief, 1986, Journal of medical genetics.

Mesenchymal Dysplasia in a Monochorionic Diamniotic Twin Pregnancy With Review of the Differential Diagnosis of Cystic Changes in the Placenta

L. Geerts, H. Wainwright, G. de Jong, 2007, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Somatic mutations of the APC, KRAS, and TP53 genes in nonpolypoid colorectal adenomas

E. Jaramillo, P. Slezak, V. Hayes, 2000, Genes, chromosomes & cancer.

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

D. Zaharie, S. Bardien, L. van der Merwe, 2009, British journal of neurosurgery.

Chromosome 22q11 in a Xhosa schizophrenia population.

R. Emsley, D. Niehaus, L. Koen, 2012, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Heavy Prenatal Alcohol Exposure is Related to Smaller Corpus Callosum in Newborn MRI Scans

Lilla Zöllei, J. Jacobson, S. Warfield, 2017, Alcoholism, clinical and experimental research.

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

S. Bardien, L. van der Merwe, J. Greinwald, 2009, BMC Medical Genetics.

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

M. Christiansen, S. Bardien, G. de Jong, 2010, Biochemical and biophysical research communications.

Antenatal ultrasonographic findings in tuberous sclerosis. Report of 2 cases.

G. de Jong, R. Hewlett, J. Shires, 1986, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.