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Retricted access

Research article

First published 2018-5

Grey wolf optimization based clustering of hybrid fingerprint for efficient de-duplication

Jyoti Malhotra, Jagdish Bakal

Multiagent and Grid Systems

Open access

Case report

First published 2023

A de novo chromosome 9p duplication in a female child with short stature and developmental delay

Tinatin Tkemaladze, Kakha Bregvadze, Nikoloz Papiashvili [...]

Sage Open Medical Case Reports

Open access

Research article

First published 2026-1

A comprehensive framework for de-duplication: Acute kidney failure (AKF) case study

Chomchanok Yawana, Wachiranun Sirikul, Juggapong Natwichai

Health Informatics Journal

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Research article

First published 2021-09-15

An efficient technique for cloud storage using secured de-duplication algorithm

Prakash Mohan, Manikandan Sundaram, Sambit Satpathy [...]

Journal of Intelligent & Fuzzy Systems: Applications in Engineering and Technology

Open access

Case report

First published 2019

De Novo Duplication in the CHD7 Gene Associated With Severe CHARGE Syndrome

Laura Pranckėnienė, Eglė Preikšaitienė, Lucie Gueneau [...]

Genomics Insights

Open access

Research article

First published 2024-8

Prenatal diagnosis and genetic counseling of a de novo 10q11.21q11.23 duplication associated with a normal phenotype

Liu Ouyang, Yan Li, Fangfang Liu [...]

Journal of International Medical Research

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Other

First published 2011-2

Congenital Hypotonia in a Child With a De Novo 22q13 Monosomy and 2pter Duplication: A Clinical and Molecular Genetic Study

Antonio Trabacca, Luciana Losito, Marta De Rinaldis [...]

Journal of Child Neurology

Free access

Case report

First published 2020

Muscular,Ocular and Brain Involvement Associated with a De Novo 11q13.2q14.1 Duplication: Contribution to the Differential Diagnosis of Muscle-Eye-Brain Congenital Muscular Dystrophy

Rocío N. Villar-Quiles, Marta Gomez-Garcia de la Banda, Annie Barois [...]

Journal of Neuromuscular Diseases

Retricted access

Research article

First published 2019-6

India as database: Response to Reetika Khera

Lawrence Cohen

Contributions to Indian Sociology

Retricted access

Research article

First published 2010-02

Clinical,Cytogenetic,and Molecular Characterization of a Girl with Some Clinical Features of Down Syndrome Resulting from a Pure Partial Trisomy 21q22.11-qter Due to a De Novo Intrachromosomal Duplication

Alicia Vaglio, Aubrey Milunsky, Andrea Quadrelli [...]

Genetic Testing and Molecular Biomarkers

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