Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11970
Title: Phenotype-genotype complexities: opening DOORS.
Austin Authors: Berkovic, Samuel F ;Gecz, Jozef
Affiliation: Epilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
School of Paediatrics and Reproductive Health, The University of Adelaide at the Women's and Children's Hospital, North Adelaide, Adelaide SA 5006, Australia
Issue Date: 29-Nov-2013
Publication information: The Lancet. Neurology 2013; 13(1): 24-5
Gov't Doc #: 24291219
URI: https://ahro.austin.org.au/austinjspui/handle/1/11970
DOI: 10.1016/S1474-4422(13)70237-0
Journal: The Lancet. Neurology
URL: https://pubmed.ncbi.nlm.nih.gov/24291219
Type: Journal Article
Subjects: Carrier Proteins.genetics
Craniofacial Abnormalities.genetics
Exome.genetics
Female
Hand Deformities, Congenital.genetics
Hearing Loss, Sensorineural.genetics
Humans
Intellectual Disability.genetics
Internationality
Male
Nails, Malformed.genetics
Phenotype
Sequence Analysis, DNA.methods
Appears in Collections:Journal articles

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