Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism

Παρόμοια τεκμήρια

• Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism
  ανά: Fu, Chunyun, κ.ά.
  Έκδοση: (2016)
• The incidence of congenital hypothyroidism (CH) in Guangxi, China and the predictors of permanent and transient CH
  ανά: Fu, Chunyun, κ.ά.
  Έκδοση: (2017)
• de novo interstitial deletions at the 11q23.3-q24.2 region
  ανά: Su, Jiasun, κ.ά.
  Έκδοση: (2016)
• Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability
  ανά: Zhang, Shujie, κ.ά.
  Έκδοση: (2016)
• Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3)
  ανά: Chen, Rongyu, κ.ά.
  Έκδοση: (2014)