Maternal Uniparental Disomy of Chromosome 1 with No Apparent Phenotypic Effects
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
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3. Complete Paternal Uniparental Disomy of Chromosome 2 in an Asian Female Identified by Short Tandem Repeats and Whole Genome Sequencing;Cytogenetic and Genome Research;2019
4. Genomic imprinting;The AGT Cytogenetics Laboratory Manual;2017-03-04
5. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronicNTRK1-mutation due to uniparental disomy;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-05-17
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