Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon ; volume:8 ; number:1 ; day:11 ; month:9 ; year:2018 ; pages:1-2 ; date:12.2018
Scientific reports ; 8, Heft 1 (11.9.2018), 1-2, 12.2018

Classification: Allgemeines, Wissenschaft

Creator: Mathur, Praveen

Contributor: Medicherla, Krishna Mohan
Chaudhary, Spandan
Patel, Mruduka
Bagali, Prashanth
Suravajhala, Prashanth
SpringerLink (Online service)

DOI: 10.1038/s41598-018-32119-5

URN: urn:nbn:de:101:1-2018102723225762914704

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

Last update: 14.08.2025, 10:59 AM CEST

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Mathur, Praveen
Medicherla, Krishna Mohan
Chaudhary, Spandan
Patel, Mruduka
Bagali, Prashanth
Suravajhala, Prashanth
SpringerLink (Online service)

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Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon

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Other Objects (12)

Whole exome sequencing reveals rare variants linked to congenital pouch colon

Exome variants associated with asthma and allergy

Exome sequencing for diagnosis of congenital hemolytic anemia

Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Identification of copy number variants from exome sequence data

Annotation of human exome gene variants with consensus pathogenicity

Identifying rare variants from exome scans: the GAW17 experience

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

X-linked congenital adrenal hypoplasia: a case presentation

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

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Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing

Whole exome sequencing reveals rare variants linked to congenital pouch colon

Exome variants associated with asthma and allergy

Exome sequencing for diagnosis of congenital hemolytic anemia

Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Identification of copy number variants from exome sequence data

Annotation of human exome gene variants with consensus pathogenicity

Identifying rare variants from exome scans: the GAW17 experience

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

X-linked congenital adrenal hypoplasia: a case presentation

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

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Whole exome sequencing reveals rare variants linked to congenital pouch colon

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Exome sequencing for diagnosis of congenital hemolytic anemia

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Identification of copy number variants from exome sequence data

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Identifying rare variants from exome scans: the GAW17 experience

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