Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes ; volume:12 ; number:1 ; day:7 ; month:12 ; year:2022 ; pages:1-11 ; date:12.2022
Scientific reports ; 12, Heft 1 (7.12.2022), 1-11, 12.2022

Creator: Ganesh, Suhas
Vemula, Alekhya
Bhattacharjee, Samsiddhi
Mathew, Kezia
Ithal, Dhruva
Navin, Karthick
Nadella, Ravi Kumar
Viswanath, Biju
Sullivan, Patrick F.
Jain, Sanjeev
Purushottam, Meera

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-022-25664-7

URN: urn:nbn:de:101:1-2023021721073422038345

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

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Associated

Ganesh, Suhas
Vemula, Alekhya
Bhattacharjee, Samsiddhi
Mathew, Kezia
Ithal, Dhruva
Navin, Karthick
Nadella, Ravi Kumar
Viswanath, Biju
Sullivan, Patrick F.
Jain, Sanjeev
Purushottam, Meera
SpringerLink (Online service)

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Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes

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Other Objects (12)

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