Related Experiment Videos

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G

M Shohat¹, N Fischel-Ghodsian, C Legum

¹Department of Medical Genetics, Rabin Medical Center, Petah Tiqva, Israel.

American Journal of Otolaryngology

|February 9, 1999

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type.

Clinical genetics·2017

Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2017

Homozygous deletion of RAG1, RAG2 and 5' region TRAF6 causes severe immune suppression and atypical osteopetrosis.

Clinical genetics·2016

Controversies in counseling for mitochondrial conditions.

Journal of genetic counseling·2013

High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel.

Clinical genetics·2011

Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype.

Clinical genetics·2008

See all related articles