Pages that link to "Q35770210"

The following pages link to Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. (Q35770210):

Displaying 12 items.

• A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report (Q35845586) (← links)
• THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome (Q37297770) (← links)
• The Missing Link: A Case of Absent Pituitary Infundibulum and Ectopic Neurohypophysis in a Pediatric Patient with Heterotaxy Syndrome (Q47107088) (← links)
• Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities (Q49653037) (← links)
• Update on investigations pertaining to the pathogenesis of biliary atresia (Q50075063) (← links)
• BILIARY ATRESIA: Clinical and Research Challenges for the 21st Century. (Q52617019) (← links)
• A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 (Q57112027) (← links)
• Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation (Q64264952) (← links)
• Exome Sequencing in Individuals with Isolated Biliary Atresia (Q89747881) (← links)
• Pituitary Transcription Factor Mutations Leading to Hypopituitarism (Q90540512) (← links)
• Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome (Q91140075) (← links)
• The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance (Q92967255) (← links)