Sreelata Nair

Sreelata Nair

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Sreelata Nair

Sreelata Nair

Publications by authors named "Sreelata Nair"

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Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa.

F1000Res 2016 17;5:900. Epub 2016 May 17.

GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Delhi, India; Academy of Scientific and Innovative Research, CSIR-IGIB South Campus, Delhi, India.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926754PMC
http://dx.doi.org/10.12688/f1000research.8380.2DOI Listing
August 2016

Dysmorphic features and congenital heart disease in chromosome 6q deletion: A short report.

Indian J Hum Genet 2012 Jan;18(1):127-9

Department of Fetal Medicine, Lifeline Genetics and Research Centre, Lifeline Super Specialty Hospital, Adoor, Pathanamthitta, Kerala, India.

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http://dx.doi.org/10.4103/0971-6866.96682DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385170PMC
January 2012