Associated Papers
Genomic and transcriptional characterization of early esophageal squamous cell carcinoma.
Zhao J et al.
Bmc Medical Genomics, 2023
A novel mutation of HOXA11 in a patient with septate uterus.
Zhu Y et al.
Orphanet Journal of Rare Diseases, 2017
A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.
Cao L et al.
Journal of Genetics, 2017
Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1.
Wallis M et al.
American Journal of Medical Genetics. Part A, 2016
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