Search Result "uniparental disomy"


Book of Abstract

Uniparental Disomy as a Mechanism for Combined Oxidative PhosphorylationDeficiency Associated with MRPS34 Gene

Journal: Endocrine, Metabolic & Immune Disorders - Drug Targets
Volume: 24 Issue: 16 Year: 2024 Page: 25-25
Author(s):

Systematic Review Article

Clinical and Molecular Heterogeneity of Silver-Russell Syndrome andTherapeutic Challenges: A Systematic Review

Journal: Current Pediatric Reviews
Volume: 19 Issue: 2 Year: 2023 Page: 157-168
Author(s):

The Application of Single Nucleotide Polymorphism Microarrays in Cancer Research

Journal: Current Genomics
Volume: 8 Issue: 4 Year: 2007 Page: 219-228
Author(s): Xueying Mao, Bryan D. Young, Yong-Jie Lu

Molecular Pathogenesis of Philadelphia Chromosome Negative Chronic Myeloproliferative Neoplasms

Journal: Current Cancer Drug Targets
Volume: 11 Issue: 1 Year: 2011 Page: 20-30
Author(s): R. Jager, R. Kralovics

From Genomic Imprinting to Developmental Physiology: Identifying Stepping Stones

Journal: Current Pharmacogenomics
Volume: 2 Issue: 3 Year: 2004 Page: 233-242
Author(s): Bernard Dan, Stewart G. Boyd, Guy Cheron

Use of Single Nucleotide Polymorphism Array Technology to Improve the Identification of Chromosomal Lesions in Leukemia

Journal: Current Cancer Drug Targets
Volume: 13 Issue: 7 Year: 2013 Page: 791-810
Author(s): Ilaria Iacobucci, Annalisa Lonetti, Cristina Papayannidis, Giovanni Martinelli

Clinical Features, Medical Issues, and Diagnostic Testing in Angelman Syndrome

Ebook: Angelman Syndrome: Communication, Educational and Related Considerations
Volume: 1 Year: 2015
Author(s): Jennifer M. Mueller,Charles A. Williams
Doi: 10.2174/9781681081168115010006

Human Imprinting Anomalies in Fetal and Childhood Growth Disorders: Clinical Implications and Molecular Mechanisms

Journal: Current Pharmaceutical Design
Volume: 20 Issue: 1 Year: 2014 Page: 1751-1763
Author(s): Salah Azzi, Frederic Brioude, Yves Le Bouc, Irene Netchine

Cytogenetic and Molecular Abnormalities in Myelodysplastic Syndrome

Journal: Current Molecular Medicine
Volume: 11 Issue: 8 Year: 2011 Page: 678-685
Author(s): H. Nagoshi, S. Horiike, J. Kuroda, M. Taniwaki

Significance of Genome-Wide Analysis of Copy Number Alterations and UPD in Myelodysplastic Syndromes using Combined CGH – SNP Arrays

Journal: Current Medicinal Chemistry
Volume: 19 Issue: 22 Year: 2012 Page: 3739-3747
Author(s): Ausaf Ahmad,M. Anwar Iqbal

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