Publications by authors named "Ralph Oertel"

6Publications

Molecular Karyotyping in Children and Adolescents with Gender Dysphoria.

Transgend Health 2018 1;3(1):147-153. Epub 2018 Aug 1.

Department of Adolescent Medicine, Royal Children's Hospital, Parkville, Australia.

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http://dx.doi.org/10.1089/trgh.2017.0051DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083207PMC
August 2018

Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction.

Genes (Basel) 2018 Jun 7;9(6). Epub 2018 Jun 7.

Cyto-Molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, 3052 Victoria, Australia.

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http://www.mdpi.com/2073-4425/9/6/287
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http://dx.doi.org/10.3390/genes9060287DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027392PMC
June 2018

FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts.

Genet Med 2018 12 29;20(12):1627-1634. Epub 2018 Mar 29.

Cyto-Molecular Diagnostic Research Laboratory, Victorian Clinical Genetics Services and Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.

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http://dx.doi.org/10.1038/gim.2018.52DOI Listing
December 2018

Clinical audit of genetic testing and referral patterns for fragile X and associated conditions.

Am J Med Genet A 2016 06 18;170(6):1439-49. Epub 2016 Feb 18.

Genetics Education and Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, VIC, Australia.

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http://dx.doi.org/10.1002/ajmg.a.37603DOI Listing
June 2016