Detalhe da pesquisa
1.
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.
Am J Hum Genet
; 108(5): 857-873, 2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33961779
2.
Scaling national and international improvement in virtual gene panel curation via a collaborative approach to discordance resolution.
Am J Hum Genet
; 108(9): 1551-1557, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34329581
3.
Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate.
Hum Mutat
; 41(11): 1884-1891, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32906196
4.
Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol.
BMJ Open
; 14(4): e081426, 2024 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38569677
5.
Distinct diagnostic trajectories in NBAS-associated acute liver failure highlights the need for timely functional studies.
JIMD Rep
; 63(3): 240-249, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35433172