Results 191 to 200 of about 31,332 (279)

Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia [PDF]

open access: bronze, 2003
Safarina G. Malik   +4 more
openalex   +1 more source

A novel GATA3 frameshift mutation causes hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome. [PDF]

open access: yesMol Genet Metab Rep
Huang B   +8 more
europepmc   +1 more source

Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family [PDF]

open access: bronze, 2003
Safarina G. Malik   +7 more
openalex   +1 more source

Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature. [PDF]

open access: yesBMC Endocr Disord, 2019
Joseph ADD   +7 more
europepmc   +1 more source

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