Associated Papers
Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type.
Wu J et al.
Frontiers in Genetics, 2022
35368703 (PubMed )
Supplement: DataSheet1.zip › 823861_SupMaterial › Data_Sheet_1.ZIP › raw_datas › patient_2__NGS_raw_data.xlsx › Sheet1
FOXE1 gene mutation screening by multiplex PCR/DHPLC in CHARGE syndrome and syndromic and non-syndromic cleft palate.
Venza M et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 2006
Gene symbol: FOXE1. Disease: Nonsyndromic cleft palate. Accession #Hm0535.
Teti D et al.
Human Genetics, 2006
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