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Lista de obras de Masoumeh Falah

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.

artículo científico publicado en 2010

A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family

artículo científico publicado en 2011

Association of genetic variations in the mitochondrial DNA control region with presbycusis

artículo científico publicado en 2017

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

artículo científico publicado en 2016

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.

artículo científico publicado en 2010

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

artículo científico publicado en 2011

Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment

artículo científico publicado en 2016

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

artículo científico publicado en 2006

Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome.

artículo científico publicado en 2008

The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis

scientific article published on 19 October 2016

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