Familial 22q11.2 deletion syndrome with autosomal dominant inheritance

Lignende værker

• Palatoschisis, Schizophrenia and Hypocalcaemia: Phenotypic Expression of 22q11.2 Deletion Syndrome (DiGeorge Syndrome) in an Adult
  af: Melissa Elise van der Meijs, et al.
  Udgivet: (2021-04-01)
• Hypoparathyroidism concomitant with macrothrombocytopenia in an elderly woman with 22q11.2 deletion syndrome
  af: Hsiu-Chien Yang, et al.
  Udgivet: (2018-10-01)
• Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies
  af: Paula Sandrin-Garcia, et al.
  Udgivet: (2007-01-01)
• 22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment
  af: Leyla S. Namazova-Baranova, et al.
  Udgivet: (2016-12-01)
• Case report: Novel phenotype in central 22q11.2 deletion syndrome
  af: Patrick Dideum, et al.
  Udgivet: (2020-12-01)