Number of items: 2.
Journal Article
Singh, Nivedita and Bhat, Vishwanath Kumble and Tiwari, Ankana and Kodaganur, Srinivas G and Tontanahal, Sagar J and Sarda, Astha and Malini, K V and Kumar, Arun
(2017)
A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family.
In: HUMAN MOLECULAR GENETICS, 26
(6).
pp. 1104-1114.
Kodaganur, Srinivas G and Tontanahal, Sagar J and Sarda, Astha and Shah, Mohd H and Bhat, Vishwanath and Kumar, Arun
(2013)
Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome.
In: Clinical Dysmorphology, 22
(2).
pp. 54-58.
This list was generated on Wed Apr 24 20:15:14 2024 IST.
