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chromosome 16
(tissue)
Summary
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Body Atlas
Curated Studies
Most Correlated Studies
Acute myeloid leukemia by karyotype and by discrete mutation
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Most Relevant Literature
Morquio A syndrome due to maternal uniparental isodisomy of the telomeric end of chromosome 16.
Primary ciliary dyskinesia with HYDIN gene mutations in a child and literature review].
Two adjacent mutations on chromosome 16 discovered in a patient presenting with generalized convulsi…
A novel pseudo-dicentric variant of 16p11.2-q11.2 contains euchromatin from 16p11.2-p11.1 and resemb…
A boy with Meier-Gorlin syndrome carrying a novel ORC6 mutation and uniparental disomy of chromosome…
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Non-invasive Placental Chromosome Exploration of Intrauterine Growth Restriction
Validate Non-invasive Prenatal Tests for the Detection of Chromosomal Abnormalities
Prenatal Screening, Diagnosis and Intrauterine Intervention of Fetal Abnormal Chromosome and Structu…
Endocrine, Metabolic, Cardiovascular and Immunological Aspects of Sex Chromosome Abnormalities in Re…
Defining an Obesity QTL on Chromosome 3q
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