Genomics

Dataset Information

0

SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystrophy and Bosma Arhinia and microphtalmia syndrome (Methylation).

ABSTRACT: Determination of SMCHD1 epi-signature in type 2 Facio Scapulo Humeral Dystrophy (FSHD2) and Bosma Arhinia and Microphtalmia Syndrome (BAMS).

ORGANISM(S): Homo sapiens

PROVIDER: GSE175527 | GEO | 2023/12/31

REPOSITORIES: GEO

Json Xml

Similar Datasets

Unknown SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome (ChIP-Seq).
2023-12-31 | GSE174769 | GEO
Unknown SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome. [ChIP-Seq]
2022-05-27 | GSE179984 | GEO
Unknown SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome. [RNA-Seq]
2022-05-27 | GSE174604 | GEO
Genomics SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome.
| PRJNA746136 | ENA
Genomics SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome. [ChIP-Seq]
| PRJNA746140 | ENA
Genomics SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome. [RNA-Seq]
| PRJNA730717 | ENA
Genomics Weakened sarcomeric contractility distinguishes Facio Scapulo Humeral Dystrophy muscle fibers
| PRJNA717762 | ENA
Unknown SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome.
2022-05-27 | GSE179986 | GEO
Unknown Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report.
| S-EPMC5025538 | biostudies-literature
Unknown Weakened sarcomeric contractility distinguishes Facio Scapulo Humeral Dystrophy muscle fibers
2022-02-18 | GSE169724 | GEO