S. Shaw

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

H. McDermid, A. Wong, M. C. Phelan, 2003, Journal of medical genetics.

22q13 deletion syndrome.

H. McDermid, R. C. Rogers, R. Saul, 2001, American journal of medical genetics.

VACTERLS ASSOCIATIONWITH PULMONARY ARTERIAL HYPERTENSION AND LEAST VERTEBRAL ANOMALY

R. Raj, Braja Kishore Behera, S. Shaw, 2016 .

Mammoth Ovarian Tumour in Pregnancy: A Case Report

A. Nayak, B. Nayak, A. Periyasamy, 2015, Indian Journal of Gynecologic Oncology.