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1.
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing.
Ann Hum Genet
; 86(4): 181-194, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35118659
2.
Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys.
Mol Genet Genomic Med
; 10(2): e1868, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34997822
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