A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient.

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🔗 View Article (PMC 4297881)

Published in Meta Gene on November 25, 2014

Authors

Rashmi Patel¹, Fanish Mani Tripathi², Subodh Kumar Singh³, Anjali Rani⁴, Visweswar Bhattacharya⁵, Akhtar Ali⁶

Author Affiliations

1: Centre for Genetic Disorders, Faculty of Science, Banaras Hindu University, Varanasi, India.
2: Swami Harshankranand Ji Hospital & Research Center, Varanasi, India.
3: G S Memorial Plastic Surgery Hospital & Trauma Center, Varanasi, India.
4: Department of Obstetrics & Gynaecology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
5: Department of Plastic Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
6: Centre for Genetic Disorders, Faculty of Science, Banaras Hindu University, Varanasi 221005, U.P., India.

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