Chintana Tochareontanaphol

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New Mutations of the ID1 Gene in Acute Myeloid Leukemia Patients

Somying Promso, S. Paca-uccaralertkun, Thivaratana Sinthuwiwat, 2015, Pathobiology.

Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion

V. Praphanphoj, A. Mutirangura, P. Kantaputra, 2006, American journal of medical genetics. Part A.

Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: report of a four-generation Thai family.

B. Schutte, Y. Sumitsawan, P. Kantaputra, 2002, American journal of medical genetics.