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chromosomes human, pair 16
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NextBio Summary
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Body Atlas
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Acute myeloid leukemia by karyotype and by discrete mutation
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Morquio A syndrome due to maternal uniparental isodisomy of the telomeric end of chromosome 16.
Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of …
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…
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PGS Using Microarray in IVF Patients With Repeated Implantation Failure
Molecular Epidemiology of Childhood Leukemia (Aka The California Childhood Leukemia Study)
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