Cargando…
Maternal UPD of chromosome 7 in a patient with Silver‐Russell syndrome and Pendred syndrome
BACKGROUND: Silver‐Russell syndrome (SRS) is a heterogeneous imprinting disorder featuring severe intrauterine and postnatal growth retardation and dysmorphic features. Pendred syndrome (PDS) is an autosomal recessive disorder caused by mutations in the SLC26A4 gene characterized by sensorineural he...
Autores principales: | Zhang, Chuan, Hao, Shengju, Zhang, Qinghua, Liu, Furong, Zhou, Bingbo, Xuan, Feng, Xing, Wang, Chen, Xue, Wang, Yan, Ma, Panpan, Cao, Zongfu, Ma, Xu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521231/ https://www.ncbi.nlm.nih.gov/pubmed/32666542 http://dx.doi.org/10.1002/jcla.23407 |
Ejemplares similares
-
Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features
por: Cirello, Valentina, et al.
Publicado: (2018) -
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome
por: Pignata, Laura, et al.
Publicado: (2021) -
Mosaic UPD(7q)mat in a patient with silver Russell syndrome
por: Su, Jiasun, et al.
Publicado: (2017) -
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
por: Tannorella, Pierpaola, et al.
Publicado: (2021) -
Pendred Syndrome, or Not Pendred Syndrome? That Is the Question
por: Tesolin, Paola, et al.
Publicado: (2021)