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1.
Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing.
Mol Biol Rep
; 51(1): 662, 2024 May 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-38767670
2.
Second report of TEDC1-related microcephaly caused by a novel biallelic mutation in an Iranian consanguineous family.
Mol Biol Rep
; 51(1): 181, 2024 Jan 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-38252227
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