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Sultana Muhammad Hussein Faradz (Sultana M H Faradz, Sultana Mh Faradz)

Publication Activity (10 Years)

Years Active: 2019-2020
Publications (10 Years): 3

Top Topics

Intellectual Disability

Mitochondrial Dna

Top Venues

American journal of medical genetics. Part A

Annals of laboratory medicine

BMJ case reports

Diponegoro University

University of New South Wales - Randwick Campus (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Diponegoro University Jan 1o 1979

Indonesia

Professor :: center for Biomedical Research

Education History

University of New South Wales - Randwick Campus

Australia

PHD :: Pathology Medical Genetics

Publications

Nydia Rena Benita Sihombing, Tri Indah Winarni, Hans van Bokhoven, Ineke van der Burgt, Nicole de Leeuw, Sultana Muhammad Hussein Faradz
Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism. American journal of medical genetics. Part A 182 (11) (2020)
Gara Samara Brajadenta, Agustini Utari, Sylvie Patri, Frederic Bilan, Sultana Muhammad Hussein Faradz, Alain Kitzis, Vincent Thoreau
Identification of a Novel CHD7 Mutation in a CHARGE Syndrome Patient in Indonesia. Annals of laboratory medicine 39 (5) (2019)
Nydia Rena Benita Sihombing, Nicole de Leeuw, Hans van Bokhoven, Sultana Muhammad Hussein Faradz
Duplication of 1q31.3q41 in two affected siblings due to paternal insertional translocation. BMJ case reports 12 (8) (2019)