Author

Maria Kamarinos

Observed name: M. Kamarinos

Observed institutions: Royal Children's Hospital, The University of Melbourne, Victorian Clinical Genetics Services, Murdoch Children's Research Institute

OpenAlex ID: A5080215437

High frequency hearing loss correlated with mutations in the GJB2 gene

2000 · Stephen A Wilcox, Kerryn Saunders, et al. · Human Genetics · 201

40th EASD Annual Meeting of the European Association for the Study of Diabetes

2004 · M. Veitenhansl, K. Stegner, et al. · Diabetologia · 70

Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

2001 · Maria Kamarinos, Jim McGill, et al. · Human Mutation · 60

Prevalence and nature of connexin 26 mutations in children with non‐syndromic deafness

2001 · Hans‐Henrik M Dahl, Kerryn Saunders, et al. · The Medical Journal of Australia · 43

Erratum: Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families Communicated by Mark H. Paalman Online Citation: Human Mutation, Mutation in Brief #464 (2001) Online http://www.interscience.wiley.com/jpages/1059-7794/pdf/mutation/464.pdf Original Reference: Kamarinos et al., Human Mutation, 17:351 (2001).

2001 · Maria Kamarinos, Jim McGill, et al. · Human Mutation · 2

Erratum: "Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness" (Medical Journal of Australia (2001) vol. 175 (191-194))

2004 · H H Dahl, Kerryn Saunders, et al. · The Medical Journal of Australia

Works count: 7

Citation count: 376

H-index: 4

I10-index: 4