Pages that link to "Q56322223"

The following pages link to Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay (Q56322223):

Displaying 14 items.

• The Role of Hedgehog Signaling in Tumor Induced Bone Disease (Q26783615) (← links)
• Infantile hydrocephalus: a review of epidemiology, classification and causes (Q35101052) (← links)
• Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets (Q36017094) (← links)
• Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas (Q37044374) (← links)
• Non-melanoma skin cancer: new and future synthetic drug treatments. (Q38729673) (← links)
• Diagnosis and Management of Hereditary Basal Cell Skin Cancer (Q38807597) (← links)
• Early therapy-related myeloid sarcoma and deletion of 9q22.32 to q31.1. (Q50674980) (← links)
• Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci. (Q54764863) (← links)
• Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies (Q56266807) (← links)
• The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes (Q57266419) (← links)
• Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data (Q58585710) (← links)
• De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental Delay (Q64063541) (← links)
• Unexpected phenotype in a frameshift mutation of PTCH1 (Q90444164) (← links)
• A novel INDEL mutation in the PTCH1 gene in a Chinese family with Gorlin syndrome (Q92714973) (← links)