Genome-wide association study in craniosynostosis condition using innovative systematic bioinformatic analysis tools and techniques: Future prospective and clinical practice | Zendy

Mayadhar Barik | Zendy; Minu Bajpai | Zendy; Arun Malhotra | Zendy; JyotishC Samantaray | Zendy; Sadananda Dwivedi | Zendy; Sambhunath Das | Zendy

Open Access

Genome-wide association study in craniosynostosis condition using innovative systematic bioinformatic analysis tools and techniques: Future prospective and clinical practice

Author(s) -

Mayadhar Barik,

Minu Bajpai,

Arun Malhotra,

JyotishC Samantaray,

Sadananda Dwivedi,

Sambhunath Das

Publication year - 2018

Publication title -

journal of pediatric neurosciences

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.247

H-Index - 18

eISSN - 1998-3948

pISSN - 1817-1745

DOI - 10.4103/jpn.jpn_71_17

Subject(s) - medicine , craniosynostosis , genome wide association study , clinical practice , computational biology , medline , bioinformatics , genetics , single nucleotide polymorphism , family medicine , surgery , genotype , gene , biology , political science , law

Craniosynostosis (CS) conditions are included with the premature fusion of one or more multiple cranial sutures. As the second leading and most common craniofacial anomaly and orofacial clefts globally. Syndromic and nonsyndromic CS (NSCS) occur as a part of a genetic syndrome unlike Apert, Crouzon, Pfeiffer, Muenke, and Saethre-Chotzen syndromes. Approximately, 90% of the cases of CS arises from NSCS group and it is now a great challenge for the researcher and neurosurgeon for Indian-origin children, a great burden worldwide.

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