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1.
Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems.
Mol Syndromol
; 11(2): 62-72, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32655337
2.
Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability.
Gene
; : 144918, 2020 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32621952
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